What Research Scientist Opportunities Jobs are in Hong Kong?

**HOW MIGHT YOU DEFY IMAGINATION?**
Amgen is one of the world's leading independent biotechnology companies. For over 4 decades, Amgen has pioneered biotechnology breakthroughs, to bring state-of-the-art medicines from laboratory to the patient. Amgen has not only discovered and developed innovative human therapeutics but has also invested in cutting edge manufacturing capability and support services to deliver these exciting therapies to medical teams around the world. Japan and Asia Pacific (JAPAC) is the fastest growing region in Amgen. Now we are hiring a **Medical Science Liaison - Cardiovascular** in **Hong Kong** .
**Live**
**What you will do**
The Medical Scientific Liaison is a point of medical contact for their allocated product(s). The Medical Scientific Liaison leads adaptation of global/regional strategy to reflect local/regional priorities for their product(s) and/or supports execution of those strategies to improve Amgen's value proposition of inline and pipeline products in alignment with product strategies.
**Responsibilities**
+ Support development and execution of patient-focused medical strategies that improve the value proposition of Amgen's therapies including annual planning and goal setting, launch support and lifecycle management, in collaboration with Hong Kong Medical Lead and/or appropriate cross-functional teams and governance
+ Foster and enhance collaboration and coordination across Medical
+ Develop/support and lead/support execution of the strategy for medical evidence generation that shapes our products and informs the practice of medicine ensuring key needs are met in alignment with global product medical and relevant brand strategy
+ May develop and manage medical product budget
+ Ensure conduct of medical activities in full compliance of all laws, regulations and SOPs
+ Determine scientific/medical subject matter appropriateness of labels/regulatory/reimbursement/policy/promotional and medical deliverables (eg, slide decks, publications, educational activities) used to support internal/external interactions via appropriate review process
+ Lead/support the development of data interpretation, analysis and communication for medical executed studies
+ Use global infrastructure for tracking, measuring and evaluating performance and ensure continuous performance improvement
**Internally**
+ Contribute to cross functional collaborator teams in shaping the healthcare ecosystem by enabling access to medicines through evidence generation, communication and education of medical and economic value
+ Develop and/or contribute to execution of advocacy plans and strategies in partnership with internal collaborators and lead relationships as appropriate
+ Partner with/support Global Regulatory Affairs and Safety (GRAAS) in risk management/minimization activities and ensure communication of the implications to internal/external collaborators
+ Ensure product/disease state/pipeline specific medical training where appropriate, may deliver training to others
+ Ensure appropriate clinical trial conduct as a key medical interface in close partnership with Global Development Operations (eg Site Management)
+ Provide strategic input into labels/regulatory/reimbursement/policy/promotional used to support internal/external interactions
+ In partnership with cross-functional team, ensure informed budget/resource trade-offs, as appropriate
+ Facilitates Investigator Sponsored Studies through Amgen governance and manage study lifecycle (including communicating with investigators, as appropriate and ensuring accurate reporting of key milestone data)
**Externally**
+ Lead/support relationships with external healthcare community, including interactions with opinion leaders, payers and societies for scientific exchange, where appropriate
+ Understand the expectations of key external collaborators to support appropriate access to Amgen therapies.
+ Foster Amgen's reputation as a science-based, innovative and patient-focused reliable partner
+ Provide support and leadership of advisory boards and other relevant meetings (eg, investigator meetings, and/or expert panels)
+ Provide decision on IME, Donations, medical grants and sponsorships, where appropriate
+ Contribute to strategy development for scientific engagement across a broad range of collaborators to strengthen external understanding of the unmet need and value of the product
+ Synthesize and integrate insights to deliver medical inputs into relevant cross-regional/functional strategies, including relevant brand strategy and translate into tactics including medical communication in all forms to external collaborators
**Win**
**What we expect of you**
**Minimum Requirements**
+ Doctorate degree & 2 years of directly related experience
+ Bachelor's degree & 3 years of directly related experience
**Preferred Requirements**
+ Demonstrated ability as a medical expert in a complex matrix environment
+ Pharmaceutical product development, product lifecycle and commercialization process knowledge with understanding of other functions; including, but not limited to, Clinical Operations, Commercial, Safety, Regulatory, Value & Access, and Medical Affairs
+ Product/therapeutic area knowledge
+ Experience in regional/local medical practice and healthcare ecosystems
+ Skilled at engagement, scientific exchange with external medical community
+ Clinical research experience
+ In-depth understanding of the scientific method and clinical applications based on medical, scientific and practical rationale
+ Familiarity with concepts of clinical research and clinical trial design, including biostatistics
+ Sound scientific and clinical judgement
+ Knowledge of Good Clinical Practices (GCP), region regulations and guidelines, and applicable international regulatory requirements
+ Familiarity of local pharmaceutical industry and legal/health system environment
+ Skilled at effectively presenting ideas and documenting complex medical/clinical concepts in both written and oral communication
+ History of solving problems while exhibiting superior judgment and a balanced, realistic understanding of issues
+ Network of medical, clinical contacts in product/therapeutic area
**Thrive**
**What you can expect of us**
As we work to develop treatments that take care of others, so we work to care for our teammates' professional and personal growth and well-being.
+ Vast opportunities to learn and move up and across our global organization
+ Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
+ Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits
**Apply now for a career that defies imagination.**
In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us.
careers.amgen.com
**Equal Opportunity Statement**
Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.

Company Description
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on LinkedIn, ( Facebook, Instagram ( , X ( and YouTube. ( Description
Guide, coordinate, plan, and prioritize the broad area of market access capabilities to design and implement innovative market access solutions into the changing market environment while driving cross-functional teamwork placing the patient at the center of any efforts and operating within AbbVie business code of conduct, policies and all applicable laws and regulations.
Responsibilities
Manage cross-functional task forces to elaborate key insights for new products (prior to Phase 3) and help better tailor clinical development to ensure optimized access and price.
+ Ensure pricing and reimbursement at national and local level is aligned to and leverages other commercial strategies in order to meet or exceed affiliate plan.
+ Work closely with other functions such as Medical and Government Affairs to build networks, understanding and close partnerships with key decision makers and leverage influence through joint programs of action in order to maximize AbbVie brands success.
+ Ensure close collaboration with Area and Global and maintain awareness and understanding of the impact of local affiliate decisions on AbbVie's global business and vice versa in order to ensure Area and Global strategies and tactics are aligned with those of the Affiliate to meet both, local and Area/Global needs to maximize momentum on delivering brand performance.
+ Anticipate and influence Contracting and Tendering situations and develop strategies in order to deal with C&T challenges and maximize their opportunities for the business.
+ Develop, lead and coach direct reports (if applicable)
+ - May, as member of the Affiliate Management Team in SBU/MBU affiliates (if applicable), role model AbbVie WWW behavior and enable the Brand Team matrix to work in order to achieve high quality strategy and execution capability in all allocated brands.
Qualifications
+ Bachelor's degree or equivalent
+ Relevant experience with proven track record of success in delivering commercial results and/or being responsible for product access to market.
+ Extensive knowledge of the healthcare environment, including deep knowledge of payer and provider mechanisms, funding flows, and legislation affecting market access of pharmaceutical products.
+ Good understanding of area healthcare systems to have an area-wide perspective for local affiliate decisions.
+ Proven track record of successful leadership, management and coaching of teams and individuals, and in having developed talent and performance managed low performers (if applicable).
+ Ability to drive complex cross-functional collaboration to involve and to align Market Access strategy with other business strategies.
+ English language proficiency verbally and in writing (for all non-English speaking countries)
+ Preferred:
- Relevant experience working within a payer and provider organization
- Relevant international health care environment experience.
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

Job Overview
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
Essential Functions
- Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
- Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
- Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
- Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
- Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
- Collaborate and liaise with study team members for project execution support as appropriate.
- If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
- If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.
Qualifications
- Bachelor's Degree Degree in scientific discipline or health care preferred. Req
- Requires at least 2 years of year of on-site monitoring experience. Req
- Equivalent combination of education, training and experience may be accepted in lieu of degree. Req
- Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.
- i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Good therapeutic and protocol knowledge as provided in company training.
- Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
- Written and verbal communication skills including good command of English language.
- Organizational and problem-solving skills.
- Effective time and financial management skills.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

**Key Accountabilities:**
**Maintenance (from initiation through close out):**
Act as Parexel's direct contact with assigned sites, assess and ensure overall integrity of study implementation and adherence to study protocol at clinical sites, and perform problem-solving to address and resolve site issues.
+ Build relationships with investigators and site staff.
+ Facilitate and support site with access to relevant study systems and ensure sites are compliant with project specific training requirements.
+ Evaluate if on-site staff assignment is still accurate and determine and implement corrective actions & follow-up, if necessary / relevant.
+ Address and resolve issues at sites, including the need for additional training, potential deficiencies in documentation, and communication.
+ Address/evaluate/resolve issues pending from the previous visit, if any.
+ Follow-up on and respond to appropriate site related questions.
+ Apply working knowledge and judgment to identify and evaluate potential data quality and data integrity issues. Determine and implement appropriate follow-up action.
+ Actively participate in Investigator and other external or internal meetings and audits & regulatory inspections as required.
+ Collect, review, and approve (if applicable) updated/amended site documentation, including regulatory documents as applicable.
+ Evaluate site recruitment plan in collaboration with the site staff on an ongoing basis and provide strategy for improvements.
+ Perform on-site visits; this includes Qualification and Initiation visits; apply judgment and knowledge to independently resolve site issues, questions and concerns.
+ Conduct remote visits/contacts as requested/needed.
+ Generate visit/contact report.
+ Evaluate overall compliance and performance of sites and site staff: provide recommendations regarding site-specific actions and use judgment and experience to assess the ability and motivation of site staff.
+ Assess & manage test article/study supply including supply, accountability and destruction/return status.
+ Review & follow-up site payment status.
+ Follow-up on CRF data entry, query status, and SAEs.
+ Conduct on-site study-specific training (if applicable).
+ Perform site facilities assessments
+ Recognize impact of study non-compliance/issues/delays/changes on study timelines and communicate study issues that require immediate action, with proposed strategy for resolution
**Overall Accountabilities from Site Identification to Close out:**
Ensure timely and accurate completion of project goals and update of applicable trial management systems.
+ Work with team members to meet project goals, provide strategy for efficient project planning and goal completion, and encourage the support of team members where required.
+ Update all appropriate Clinical Trial Management Systems (CTMS) on an ongoing basis, including performing regular reviews of site level data in clinical systems (e.g. CTMS, EDC, IVRS, and SIS) and ensure timely and high quality data entry compliance from sites, manage and submit all relevant documents to the Trial Master File (TMF), ensuring first time quality, and distribute study documents to site including configuration of Investigator Site Files if applicable and on-going maintenance for completeness and quality.
+ Ensure that assigned sites are audit and inspection ready
+ Monitor and maintain compliance with ICH-GCP and applicable international and local regulations.
+ Delegate administrative and other tasks to Administrative Support Team as needed and where appropriate. Guide Administrative Support Team members, review work, and provide feedback to manager regarding performance.
+ Show commitment and perform consistent high-quality work.
+ Maintain a positive, results-orientated work environment, building partnerships and collaborative relationships, communicating with team(s) in an open, balanced, objective manner, modeling the high performance culture values.
+ Maintain a working knowledge of and ensure compliance with applicable ICH-GCP Guidelines, international and local regulations, Parexel SOPs, other Parexel / Sponsor training requirements and study specific procedures, plans and training.
+ Ensure basic understanding of project scope, milestones, budgets, and strive for high quality, timely, and efficient delivery.
+ Provide input and feedback for Performance Development Conversation(s).
+ Proactively keep manager informed about work progress and any issues.
+ Develop expertise to become a subject matter expert.
+ Work in a self-driven capacity, with limited need for oversight.
+ Complete additional tasks in a timely manner (e.g. timesheets, expenses, metrics, etc.)
**Skills:**
+ Sound problem solving skills.
+ Able to take initiative and work independently, and to proactively seek guidance when necessary.
+ Advance presentation skills.
+ Client focused approach to work.
+ Ability to interact professionally within a client organization.
+ Flexible attitude with respect to work assignments and new learning.
+ Ability to prioritize multiple tasks and achieve project timelines; utilizing strong analytical skills to make decision autonomously due to the unpredictable nature of the issues that arise.
+ Willingness to work in a matrix environment and to value the importance of teamwork.
+ Strong computer skills including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS), and MS-Office products such as Excel and Word.
+ Strong interpersonal, verbal, and written communication skills.
+ Sense of urgency in completing assigned tasks and ability to assist others to meet study/country deliverables and preserving patient safety.
+ Effective time management in order to meet study needs, team objectives, and department goals.
+ Developing ability to work across cultures.
+ Shows commitment to and performs consistently high-quality work.
+ Ability to successfully work in a ('virtual') team environment.
+ Consulting Skills
+ Great attention to detail.
+ Able to accommodate extensive travel time requirements, according to tasks allocation/phase of the study assigned.
+ Holds a driver's license where required.
**Knowledge and Experience:**
+ Site Management experience or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology
**Education:**
+ Educated to degree level (biological science, pharmacy, or other health-related discipline preferred) or equivalent nursing qualification or other equivalent experience
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

Marketing and Market Access Manager
Requisition ID: 7968
Location:
Hong Kong, Hong Kong Island, HK
**Role Purpose**
The Marketing and market access manager leads integrated brands, launch and market access plans for Lundbeck Hong Kong's portfolio. The role drives brand growth, supports appropriate patient access and ensures strong execution across public and private healthcare channels in Hong Kong.
This is a hands-on commercial leadership role covering brand strategy, product launch, customer engagement, pricing, tender, reimbursement and access execution. The role works closely with Sales, Medical, Regulatory, Finance, Supply Chain, Compliance, and regional/global teams to deliver business priorities in a compliant and locally relevant way.
This role is focused on product and portfolio-related activities. Public education, disease awareness, patient advocacy, PR, media relations and corporate communications are not primary responsibilities.
**Key responsibilities**
1. **Brand strategy and execution**
1.
2. Develop and implement brand plans, marketing strategies and tactical activities aligned with business priorities, global/regional guidance and local compliance requirements.
3. Drive brand performance by identifying growth opportunities, shaping clear positioning and ensuring effective execution.
4. Plan and deliver product-related marketing activities, including scientific meetings, congress activities, customer engagement programs, compliant sponsorships and digital initiatives.
5. Monitor market dynamics, customer insights, competitor activities and brand performance to support timely business decisions.
6. Manage marketing budgets and evaluate activity performance, KPIs and ROI.
7. Ensure all promotional materials, brand messages and customer engagement activities comply with local regulations, industry codes and Lundbeck policies.
1. **Launch and portfolio management**
1.
2. Lead or support launch planning for new products in neuro-specialty and neuro-rare diseases, indications or formulations, including positioning, customer segmentation, key messages, access pathways, launch activities and performance tracking.
3. Support lifecycle management of existing brands and identify opportunities to maximize the full potential.
4. Partner with cross-functional teams to ensure launch readiness across marketing, medical, regulatory, pricing, access, supply and field execution.
1. **Market access, pricing and tender management**
1.
2. Develop and execute market access strategies to secure appropriate patient access across Hong Kong's public and private healthcare sectors, with a focus on access pathways rather than sales channels.
3. Lead HA formulary listing, drug committee processes, HA Cluster-level adoption, and public hospital tender management.
4. Manage pricing, contracting, reimbursement and funding opportunities, including government reimbursement, charity funding and disease-specific patient access programmes.
5. Build value propositions supported by HEOR evidence and engage policymakers, payers, hospitals and other key access stakeholders.
6. Prepare the affiliate for future launches in neurological rare diseases by shaping access pathways, pricing assumptions and stakeholder plans.
1. **Team leadership and cross-functional collaboration**
1.
2. Lead and develop the Marketing and Market Access team to build a high-performing, collaborative and accountable team.
3. Set clear priorities, objectives and KPIs, and ensure strong execution against business goals.
4. Build team capability in brand planning, launch readiness, market access, stakeholder engagement and compliant execution.
5. Provide regular feedback, coaching and performance support to enable individual development.
6. Work closely with Sales, Medical, Regulatory, Finance, Supply Chain, Compliance and regional/global teams to ensure aligned execution.
7. Provide brand, product and access-related training to the sales team to support effective field execution.
**Qualifications**
+ Bachelor's degree or above in Business, Marketing, Life Sciences, Pharmacy, Public Health or a related discipline.
+ Minimum 10 years of relevant experience in the pharmaceutical or healthcare industry, preferably with strong experience in pharmaceutical marketing.
+ Proven people management experience, including team leadership, coaching and talent development.
+ Solid experience in brand planning, product launch, customer engagement and marketing execution.
+ Experience in market access, reimbursement, pricing, tender management or hospital listing is highly preferred.
+ Good understanding of the Hong Kong healthcare environment, including public and private sectors, hospital systems, payer dynamics and access pathways.
+ Experience in CNS, specialty care or innovative medicines would be an advantage.
+ Good command of digital marketing knowledge and skills.
+ MBA or other relevant postgraduate qualification would be a plus.
**Core competencies**
+ Strong people leadership, coaching and team development skills.
+ Strategic thinking and strong commercial acumen.
+ Good analytical, planning and execution capabilities.
+ Strong communication, presentation and stakeholder management skills.
+ Ability to work effectively in a matrix environment and manage multiple priorities.
+ High learning agility, resilience and adaptability.
+ Growth mindset and ability to drive change.
+ Strong compliance mindset and sound business judgment.
**About Lundbeck**
At Lundbeck, our most important contribution is easing the burden of the millions of people living with brain disorders. Whether it is migraine, depression, or other brain disorders, patients, their carers, and society as a whole depend on us.
Through cutting edge science and strong partnerships, we develop and market some of the world's leading treatments, expanding into neuro-specialty and neuro-rare from our strong legacy within psychiatry and neurology.
The brain health challenge is real. Our commitment is real. Our impact is real.
**About Lundbeck**
At Lundbeck, our most important contribution is easing the burden of the millions of people living with brain disorders. Whether it is migraine, depression, or other brain disorders, patients, their carers, and society as a whole depend on us.
Through cutting edge science and strong partnerships, we develop and market some of the world's leading treatments, expanding into neuro-specialty and neuro-rare from our strong legacy within psychiatry and neurology.
The brain health challenge is real. Our commitment is real. Our impact is real.

HongKong- FSP- (Senior) Clinical Research Associate - Client office based with flexible Work From Home
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
**What You Will Do:**
You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:
+ Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
+ Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
+ Collaborating with investigators and site staff to facilitate smooth study conduct.
+ Performing data review and resolution of queries to maintain high-quality clinical data.
+ Contributing to the preparation and review of study documentation, including protocols and clinical study reports
**Your Profile:**
You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.
Required qualifications and experience:
+ Bachelor's degree in a scientific or healthcare-related field.
+ Minimum of 2 years of experience as a Clinical Research Associate.
+ In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
+ Strong organizational and communication skills, with attention to detail.
+ Ability to work independently and collaboratively in a fast-paced environment.
+ Willingness to travel as required (approximately 60%)
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply

**Medical Science Liaison**
Hong Kong
**Live**
**What you will** **do**
Amgen is one of the world's leading independent biotechnology companies. For over 4 decades, Amgen has pioneered biotechnology breakthroughs, to bring state-of-the-art medicines from laboratory to the patient. Amgen has not only discovered and developed innovative human therapeutics, but has invested in cutting edge manufacturing capability and support services to deliver these exciting therapies to medical teams around the world. Japan and Asia Pacific (JAPAC) is the fastest growing region in Amgen. Now we are hiring a **Medical Science Liaison** in **Hong Kong** .
**Live**
**What you will do**
**Accountabilities:**
+ Field-based medical expert in the Medical Science Liaison (MSL) group within the medical organization
+ An integral position in communicating accurate, clear, and valued information regarding our science and products to multiple levels within the medical community and are responsible for providing field observations to internal stakeholders
+ Support Regional TA Head and Country Medical Lead in developing local territory R&D Tactics
**Responsibilities:**
+ Engage with healthcare stakeholders to educate and communicate clinical and scientific data to advance the scientific platform as aligned with Amgen's corporate goals and objectives
+ Educate and communicate clinical value, outcomes and economic data to payers, providers, key stakeholders, advocacy, and access enablers
+ Respond to unsolicited inquiries consistent with the MSL compliance standards
+ Provide and/or present field observations and insights to internal stakeholders
+ Execute scientific engagement plan according to annual MSL goals and metrics
+ Develop and implement local OL plans in line with the scientific engagement plan
+ Support speaker training as requested and ensure the speakers are updated on new data
+ Support Amgen sponsored research and may serve as a study lead
+ Liaise with potential investigators in non-sponsored clinical research
+ Lead and/or participate on project teams that support MSL strategies and tactics as delegated by MSL leadership
+ Advance MSL value proposition, identify gaps, achieve results, and set an example for others to follow by consistently demonstrating Amgen values and leadership attributes. Demonstrate tact and professionalism when communicating and interacting with others
+ Lead and support congress activities as aligned with strategy
+ Compliantly collaborate with cross-functional colleagues. May serve as main point of contact
+ Maintain clinical acumen and expertise and timely completion of assigned training. May serve as a training lead
+ May serve as a New Hire Mentor and/or South East Asia (SEA) MSL mentor/trainer
**Win**
**What we expect from you**
**Basic Qualifications:**
+ Medical or scientific education or experience from similar positions
+ Advanced degree (e.g. PhD , MD) preferred or strong demonstration of equivalent combination of relevant educational and professional training
**Experience:**
+ Minimum 2-3 years of experience gained in pharmaceutical / biotech industry with MSL experience preferred
+ Experience in sales force, affiliate Medical Department or Clinical Development
+ Willingness to travel
+ Experience with clinical study management and conduct is preferred
+ Medical / scientific research experience
**Knowledge:**
+ Scientific expertise in the therapeutic area, related products, disease state, and interested in latest discoveries
+ Knowledge of value messages, clinical outcomes and patient benefits for the products
+ Has solid understanding of their country local health care system and decision-making, stays on top of changes
+ Demonstrates strong project management and presentation skills
+ Knowledge of commercialization and business practices
+ Good knowledge of clinical research, drug safety, legal and compliance environment
+ Willingness to continuously expand medical, scientific, market, and industry knowledge
**Thrive**
**What you can expect from us**
As we work to develop treatments that take care of others so we work to care for our teammates' professional
and personal growth and well-being.
+ Vast opportunities to learn and move up and across our global organization
+ Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
+ Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com ( .
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
**Job Function:**
Medical Affairs Group
**Job Sub** **Function:**
Medical Science Liaison
**Job Category:**
People Leader
**All Job Posting Locations:**
Mongkok, Kowloon, Hong Kong
**Job Description:**
**We are searching for the best talent for Senior Medical Affairs Manager.**
**Purpose:**
The Senior Medical Affairs Manager is responsible for leading the development and execution of medical strategy within assigned therapeutic area(s), providing scientific leadership that supports patient outcomes, clinical practice advancement, and business objectives.
This role drives evidence generation, scientific engagement, medical governance, and cross-functional collaboration while influencing key stakeholders and strengthening medical capabilities across the organisation.
**You will** **be responsible for** **:**
+ Leading the development and execution of integrated medical strategies and annual medical plans based on scientific insights, patient needs, clinical practice gaps, and business priorities
+ Driving evidence generation initiatives by providing strategic oversight of study concepts, protocol development, study execution, publication planning, and dissemination of scientific outcomes
+ Providing senior medical leadership in product launches, lifecycle management, and cross-functional strategic discussions, ensuring scientific credibility and compliance
+ Leading high-quality scientific engagement activities, including advisory boards, expert meetings, congress activities, and medical education programmes that address evolving healthcare needs
+ Monitoring emerging scientific evidence, clinical guidelines, competitive intelligence, and healthcare trends to generate actionable insights that inform medical and business decisions
+ Building and strengthening partnerships with key opinion leaders, medical societies, healthcare institutions, and internal stakeholders across local, regional, and global teams
+ Providing expert medical review and governance for promotional, educational, scientific, and project-related materials to ensure compliance, accuracy, andappropriate riskmanagement
+ Coaching and mentoring medical colleagues and cross-functional partners while promoting capability building, scientific excellence, and a culture of continuous learning
**Qualifications / Requirements:**
+ Advanced degree in Medicine, Pharmacy, Life Sciences, Biomedical Sciences, or a related discipline; MD, PharmD, PhD, or equivalent qualification is highly preferred
+ Minimum 10 years of relevant experience in Medical Affairs, clinical development, pharmaceutical industry, academic research, or related healthcare functionsin the Hong Kong healthcare and pharmaceutical landscape.
+ Demonstrated experience leading medical strategy development, evidence generation, scientific engagement, and medical governance activities
+ Strong understanding of GCP, healthcare compliance, regulatory requirements, medical governance frameworks, and industry standards
+ Proven ability to influence cross-functional and senior stakeholders through credible scientific leadership and strategic thinking
+ Experience designing, overseeing, or supporting evidence generation programmes, including clinical studies, investigator-sponsored research, and publication activities
+ Exceptional communication, scientific presentation, and stakeholder engagement skills with the ability to translate complex scientific data into meaningful medical insights
+ Strong leadership, coaching, and mentoring capabilities witha track recordof developing talent and building high-performing collaborative teams
**About Innovative Medicine**
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Across our therapeutic areas, we are committed to advancing science, generating meaningful evidence, and transforming patient outcomes through innovative treatments and strategic medical leadership. By combining deep scientific expertise with patient-centred insights, we help shape the future of healthcare and clinical practice.
Your unique talents will help patients on their journey to wellness while driving scientific excellence across the healthcare ecosystem.
**Required Skills:**
**Preferred Skills:**
Clinical Experience, Clinical Research and Regulations, Competitive Landscape Analysis, Cross-Functional Collaboration, Customer Centricity, Data-Driven Decision Making, Data Gathering and Analysis, Developing Others, Inclusive Leadership, Interpersonal Influence, Leadership, Medical Affairs, Medical Communications, Medical Compliance, Mentorship, Performance Measurement, Problem Solving, Relationship Building, Research and Development, Scientific Communications, Strategic Thinking

**Company Description**
_"I believe in the saying "You become like the people you surround yourself with."_
_I am incredibly grateful to be part of the AECOM team for over 8 years learning from some of the best in the business - both colleagues and clients alike._
_My colleagues and clients will be the judge if I am delivering a positive difference to their careers too."_
**Michael Hill, Sector Director, Ports and Bridges, Australia and New Zealand.**
**Come grow with us.**
AECOM is continuing to grow our Ports and Maritime capability across Australia and we are seeking experienced Design and Project Managers with a strong background in Ports, Coastal and Maritime Infrastructure design to support our expanding pipeline of major projects.
These opportunities may particularly appeal to professionals who are considering a move to Australia, whether permanently or for a period of time. For those looking for an international career experience, this could be an opportunity to work on complex maritime infrastructure projects while enjoying the lifestyle and natural environment that Australia is known for.
Equally, these roles may suit someone interested in relocating to Australia for a year or two to support key project delivery, before returning to their home market. With strong investment in ports, maritime and coastal infrastructure across the country, these roles offer the opportunity to work on impactful projects supporting trade, connectivity and coastal communities.
**Job Description**
We currently have multiple opportunities across Australia, at all levels of experience, as our project pipeline continues to expand.
These roles will play a key part in strengthening our Ports & Maritime leadership capability nationally, particularly as we continue building our senior technical, design and project management presence.
**How you'll make a difference**
+ Lead the design management and delivery of ports and maritime infrastructure projects, including port expansions, marine structures, coastal infrastructure and waterfront developments.
+ Own and manage packages of work, taking accountability for scope, program, technical delivery and client outcomes.
+ Coordinate with AECOM teams across Australia and and across the globe, leveraging our design capability to deliver complex maritime infrastructure projects. Act as the client interface, building trusted relationships with port authorities, government agencies and private sector clients.
+ Manage project delivery end-to-end, including design and commercial management, programme coordination and multidisciplinary technical integration.
+ Provide leadership across maritime and coastal engineering disciplines, ensuring designs align with industry standards and best practice. Support the growth of AECOM's Ports & Maritime capability globally, mentoring engineers and strengthening delivery teams.
**Qualifications**
**The qualities that help you thrive**
The following qualifications and experience are highly desired, but if you don't tick all the boxes you could still be a perfect fit for these roles. Please apply, all applications will be considered.
+ Significant experience as a Design Manager, Technical Lead, Project Manager or Senior Engineer within ports, coastal or maritime infrastructure projects.
+ Strong experience managing multidisciplinary design teams across complex maritime infrastructure projects.
+ Experience delivering design and planning for ports, marine structures, coastal infrastructure or waterfront developments.
+ Demonstrated ability to own and deliver packages of work within major infrastructure programs.
+ Strong client engagement and stakeholder management skills, particularly with port authorities, government agencies or major infrastructure clients.
+ Experience coordinating teams across multiple offices, regions or international delivery environments.
+ A passion for delivering infrastructure that supports coastal communities, trade and long-term economic growth.
**Additional Information**
**Why join AECOM**
AECOM is the #1 transportation design firm globally as ranked by ENR for the last 23 years running. We deliver some of the most complex ports, coastal and maritime infrastructure projects across Australia and New Zealand. By joining our teams in Australia, you'll play a key role in delivering infrastructure that supports trade, connectivity and economic development across the region.
You'll also benefit from AECOM's national and global design network, giving you the opportunity to collaborate with leading specialists across ANZ and internationally, while building your career on some of Australia's most significant maritime infrastructure projects.
**Why you'll love working with us**
+ Flexible work arrangements, including alternative start/finish times, part-time, job-sharing and hybrid work options
+ Purchase up to 6 weeks additional annual leave per year
+ Flex public holidays - swap Easter or other holidays for ones that suit you better
+ Continuous learning and growth - lunch and learns, professional development courses, financial study assistance, 5 days paid study leave, global career opportunities
**Ready to push the limits of what's possible?**
We welcome applications from individuals of all backgrounds, including those with disabilities, additional health or mental health needs, and/or neurodiverse conditions. If you require any adjustments during the hiring process, please let us know.
Applications are reviewed as they come in, and the role may close earlier than expected, so if this opportunity sounds like you, we encourage you to apply as soon as possible.
**Learn more about life at AECOM:** LinkedIn, Facebook , Instagram, X, YouTube - explore our AECOM voices, employee stories, latest projects, and much more!
AECOM acknowledges the Traditional Owners and Custodians of the lands on which we, our clients and our communities live and work around Australia. We pay our respects to their cultures and to their Elders - past, present, and emerging. We are committed to connecting to Country in our work through meaningful engagement with First Nations peoples and businesses. Find out more about our Australian Reconciliation Action Plan here: acknowledges the Traditional Owners and Custodians of the lands on which we, our clients and our communities live and work around Australia. We pay our respects to their cultures and to their Elders - past, present, and emerging. We are committed to connecting to Country in our work through meaningful engagement with First Nations peoples and businesses. Find out more about our Australian Reconciliation Action Plan here: AECOM**
AECOM is the world's trusted infrastructure consulting firm, delivering professional services throughout the project lifecycle - from advisory, planning, design and engineering to program and construction management. On projects spanning transportation, buildings, water, new energy and the environment, our public- and private-sector clients trust us to solve their most complex challenges. Our teams are driven by a common purpose to deliver a better world through our unrivaled technical and digital expertise, a culture of equity, diversity and inclusion, and a commitment to environmental, social and governance priorities. AECOM is a Fortune 500 firm and its Professional Services business had revenue of $16.1 billion in fiscal year 2025. See how we are delivering sustainable legacies for generations to come at aecom.com and @AECOM.
**Freedom to Grow in a World of Opportunity**
You will have the flexibility you need to do your best work with hybrid work options. Whether you're working from an AECOM office, remote location or at a client site, you will be working in a dynamic environment where your integrity, entrepreneurial spirit and pioneering mindset are championed.
You will help us foster a culture of equity, diversity and inclusion - a safe and respectful workplace, where we invite everyone to bring their whole selves to work using their unique talents, backgrounds and expertise to create transformational outcomes for our clients.
AECOM provides a wide array of compensation and benefits programs to meet the diverse needs of our employees and their families. We also provide a robust global well-being program. We're the world's trusted global infrastructure firm, and we're in this together - your growth and success are ours too.
Join us, and you'll get all the benefits of being a part of a global, publicly traded firm - access to industry-leading technology and thinking and transformational work with big impact and work flexibility. As an Equal Opportunity Employer, we believe in each person's potential, and we'll help you reach yours.
**ReqID:** REF58838W
**Business Line:** Transportation
**Business Group:** DCS
**Strategic Business Unit:** ANZ
**Career Area:** Engineering
**Work Location Model:** Hybrid