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Equity Research Analyst – Healthcare Sector (Hong Kong)

Position Overview:

Our client, a leading Chinese securities firm in Hong Kong, is seeking an Equity Research Analyst to cover the Healthcare sector, with a focus on Hong Kong-listed pharmaceutical companies. The ideal candidate will possess a hybrid background combining expertise in life sciences/medicine with strong financial analysis skills.

Key Responsibilities :

• Independently conduct in-depth research and analysis on Hong Kong-listed pharmaceutical enterprises, covering sub-sectors such as biotech, innovative pharmaceuticals, and healthcare services.
• Develop and maintain detailed financial models to evaluate company valuations, growth drivers, and risk exposures (e.g., regulatory approvals, patent cliffs).
• Produce high-quality, actionable research reports including thematic studies, company-specific updates, and sector reviews covering regulatory shifts, clinical trials, and product launches.
• Monitor and interpret global pharmaceutical industry trends (e.g., novel therapies, M&A, FDA/EMA regulations) and assess their impact on Hong Kong-listed equities.
• Engage with internal teams (especially mainland China-based pharmaceutical analysts) to align research views, share insights on cross-border trends, and ensure cohesive cross-market analysis.
• Communicate investment recommendations effectively through written reports, client meetings, and formal presentations tailored to both financial and non-financial audiences.
• Attend industry conferences, conduct company site visits, and network with key opinion leaders (e.g., clinicians, consultants) to enhance sector expertise.

Requirements

• Master's or higher in Life Sciences (Biochemistry, Microbiology, etc.), Medicine, Pharmacy, Finance, or Economics. Advanced degrees (PhD, MBA) or professional certifications (CFA, FRM) are strongly preferred.
• Minimum 2 years of sell-side equity research experience focusing on the healthcare/pharmaceutical sector; familiarity with Hong Kong markets and HKEX regulations is a significant advantage.
• Demonstrated ability to independently manage sector coverage, generate investment ideas, and support decision-making through rigorous analysis.
• Proficiency in translating complex scientific/medical data (e.g., clinical trial results) into investable insights.
• Strong financial modeling skills and familiarity with data analysis tools.
• Fluency in English and Mandarin (written and spoken); exceptional communication and presentation skills.

Ideal Profile

The successful candidate will be a proactive, detail-oriented analyst with a passion for the healthcare sector and the ability to work both independently and collaboratively within a cross-border team. Prior exposure to Hong Kong or Greater China equity markets is highly valued.

Our client, a leading Chinese securities firm in Hong Kong, is seeking an Equity Research Analyst to cover the Healthcare sector, with a focus on Hong Kong-listed pharmaceutical companies. The ideal candidate will possess a hybrid background combining expertise in life sciences/medicine with strong financial analysis skills.

Key Responsibilities :

• Independently conduct in-depth research and analysis on Hong Kong-listed pharmaceutical enterprises, covering sub-sectors such as biotech, innovative pharmaceuticals, and healthcare services.
• Develop and maintain detailed financial models to evaluate company valuations, growth drivers, and risk exposures (e.g., regulatory approvals, patent cliffs).
• Produce high-quality, actionable research reports including thematic studies, company-specific updates, and sector reviews covering regulatory shifts, clinical trials, and product launches.
• Monitor and interpret global pharmaceutical industry trends (e.g., novel therapies, M&A, FDA/EMA regulations) and assess their impact on Hong Kong-listed equities.
• Engage with internal teams (especially mainland China-based pharmaceutical analysts) to align research views, share insights on cross-border trends, and ensure cohesive cross-market analysis.
• Communicate investment recommendations effectively through written reports, client meetings, and formal presentations tailored to both financial and non-financial audiences.
• Attend industry conferences, conduct company site visits, and network with key opinion leaders (e.g., clinicians, consultants) to enhance sector expertise.

Requirements

• Master's or higher in Life Sciences (Biochemistry, Microbiology, etc.), Medicine, Pharmacy, Finance, or Economics. Advanced degrees (PhD, MBA) or professional certifications (CFA, FRM) are strongly preferred.
• Minimum 2 years of sell-side equity research experience focusing on the healthcare/pharmaceutical sector; familiarity with Hong Kong markets and HKEX regulations is a significant advantage.
• Demonstrated ability to independently manage sector coverage, generate investment ideas, and support decision-making through rigorous analysis.
• Proficiency in translating complex scientific/medical data (e.g., clinical trial results) into investable insights.
• Strong financial modeling skills and familiarity with data analysis tools.
• Fluency in English and Mandarin (written and spoken); exceptional communication and presentation skills.

Ideal Profile

The successful candidate will be a proactive, detail-oriented analyst with a passion for the healthcare sector and the ability to work both independently and collaboratively within a cross-border team. Prior exposure to Hong Kong or Greater China equity markets is highly valued.

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bout the program
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ur Off-Cycle Program varies in length based on program/university for undergraduate students. You will be fully immersed in our day-to-day activities.
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s a participant, you will:
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• eceive training designed to help you succeed
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• ave the opportunity to work on real responsibilities alongside fellow interns and our people
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ubmitting Your Application
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• ach applicant has the opportunity to apply to up to 4 separate business / location combinations in any given recruiting year. Any additional application will be auto withdrawn. In order to apply to an additional opportunity, you must withdraw a current application that has not been turned down.
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• single applicant should not create multiple email addresses to apply to additional opportunities

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bout the division
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lobal Investment Research delivers client-focused research in the equity, fixed income, currency and commodities markets.
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More Information

• Address 224 Waterloo Rd, Kowloon Tong, Hong Kong
• Qualification PhD

FACULTY OF SCIENCE
DEPARTMENT OF COMPUTER SCIENCE
Post-Doctoral Research Fellow / Research Assistant (AI for Healthcare) (PR0733/22-23)
Responsibilities
The appointees will be expected to assist in various research projects on AI for Healthcare. Topics include automatic generation of medical reports, patient motion analysis, and treatment effect estimation. The exact project to work on depends on the appointee's experience.

Requirements
Applicants for the Postdoctoral post should have a PhD degree in areas of artificial intelligence, machine learning, computer vision or other related disciplines, and must have no more than three years of post-qualification experience at the time of application.

Applicants for the Research Assistant post should have an honors degree or above in one of the aforementioned or other related disciplines.

Applicants are expected to have experience in developing machine learning algoirithms in PyTorch/TensorFlow. Prior experience in working on EHR data, medical images, computer vision, video analytics and/or casual inference is a plus.

The successful applicant will be offered a one-year appointment. Re-appointment thereafter will be subject to performance review, mutual agreement, and funding availability.

Application Procedure
Salary will be commensurate with qualifications and experience.
Applicants are invited to submit their applications at the HKBU e-Recruitment System ). Those who are not invited for interview 8 weeks after submission of application may consider their applications unsuccessful. Details of the University's Personal Information Collection Statement can be found at

The University reserves the right not to make an appointment for the post advertised, and the appointment will be made according to the terms and conditions applicable at the time of offer.

Review of applications is ongoing until the position is filled.

This role is for upcoming future opportunities that may arise at Fortrea.

Fortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements, we'll invite you for an interview. If you're pre-selected, our recruiter will keep in touch and let you know when the role officially opens, so we can reconfirm your interest before moving forward with an offer.

Summary of Responsibilities:

• Site management responsibility for clinical studies according to Fortrea's Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records.
• Conducts site monitoring responsibilities for clinical trials according to Fortrea's Standard Operating Procedures (SOPs), ICH guidelines and GCP; including Pre-study, Site Initiation, Process Monitoring, Routine Monitoring, and Close-out Visits.
• Prepares and implements project plans related to Clinical Monitoring responsibilities.
• Ensures the protection of subjects by verifying that informed consent procedures and protocol requirements are adhered to alongside applicable regulatory requirements.
• Safeguards data integrity by careful source document review, source document verification, query generation, and resolution against established data review guidelines on Fortrea or client data management systems.
• Confirms Site Regulatory documents and applicable eTMF/Sponsor Documents are complete and current throughout the duration of the trial.
• Guarantees that the study Investigational Product inventory and accountability is accurate and that study materials are stored securely and per protocol requirements.
• Ensures adherence to global quality control and CRA performance metrics.
• Ensures audit readiness at site level.
• Acts in the project role of a Lead CRA as assigned.
• General On-Site Monitoring Responsibilities:
• Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter subjects/patients into the study. Ensure the protection of study subjects or patients by performing eligibility review, verifying that screening, informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements.
• Ensure the integrity of the source data reported by careful source document review. Monitor data for missing or implausible data.
• Ensure study data completeness, accuracy, consistency, and compliance; identify deficiencies, deviations and discrepancies, and initiate corrective action as required.
• Ensure the resources of the Sponsor and Fortrea are spent wisely by performing the required monitoring tasks in an efficient manner, according to SOPs and established guidelines, including managing travel expenses in an economical fashion according to Fortrea travel policy.
• Travel, including air travel, may be required and is an essential function of the job.
• Prepare and submit accurate and timely trip reports.
• Independently perform eCRF review, 100% source data verification, query generation and resolution against established data review guideline with or without direct supervision, on Fortrea or client data management systems, as assigned by management.
• Assist with the administration of clinical research projects, recruiting investigators (if applicable), collecting investigator documentation and site management.
• Update, navigate, and maintain Fortrea or study/Sponsor-specific trial management tools/eClinical systems.
• Track IP shipments and supplies, as needed.
• Track and follow-up on serious adverse events as assigned.
• Work closely with the study team, align monitoring to critical study timelines ensuring study deliverables are met.
• Prepare and implement study-specific monitoring plans and site Initiation slides, as assigned.
• Attend investigators' meetings (if applicable), project team meetings and teleconferences, and others as needed.
• Present training content for site initiation.
• Assist with training of new employees (e.g., co-monitoring).
• All other duties as needed or assigned.

Qualifications (Minimum Required):

•B.A./B.S. (Life Science preferred) or equivalent healthcare experience.

•Minimum 1 year experience as CRA. Has conducted on site monitoring in Hong Kong in the past 3 months.

•In lieu of the above requirement,

-CRA II: candidates with 2 more years of CRA monitoring experience in pharmaceutical or CRO industries may be considered.

-SCRA: candidates with 3 more years of CRA monitoring experience in pharmaceutical or CRO industries may be considered.

•Basic understanding of ICH Guidelines and GCP including a basic understanding of regulatory requirements.

•Basic understanding of the clinical trial process.

•Fluent in local language and English.

Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit

Clinical Research Associate (at the rank of Technical Officer/Research Assistant I/II) in the Clinical Trials Centre (Ref:

The Clinical Trials Centre (HKU-CTC) is a leading clinical trials management platform established under The University of Hong Kong LKS Faculty of Medicine (HKUMed) and is dedicated to managing and facilitating international-standard clinical trials on new drugs, medical devices and medical technologies.  HKU-CTC offers long-term development opportunities to passionate talents who are devoted to a career in the clinical trial profession.

Clinical studies are highly sophisticated, multi-disciplinary projects that require good planning, close monitoring and synchronization of research team members and activities.  HKU-CTC's Project Operations Unit (POU) is a professional unit dedicated to facilitating clinical study planning, performance and completion in compliance with international standards and in an efficient and high-quality manner.  POU is seeking talents who are interested/experienced in practising the project management profession in clinical research.  Comprehensive on-job training will be provided.  Fresh graduates will also be considered.

Main Responsibilities:

• Act as a key contact person among clinical study centres, sponsoring companies, regulatory authorities and other stakeholders to coordinate clinical trial activities;
• Facilitate the planning, initiation and monitoring of clinical studies throughout their project life cycles, ensuring adherence to protocols and regulatory requirements;
• Assess the feasibility of clinical studies at potential sites to support study planning;
• Conduct various visits (including Pre-Study Visits (PSV), Site Initiation Visits (SIV), Site Closure Visits (COV) and Monitoring Visits (MV)) to verify compliance, data integrity, and participant safety;
• Support study planning, preparation and initiation (e.g. setting study time plans/milestones, assisting in obtaining ethics and regulatory approvals, importing study products, coordinating logistics and workflows, and organizing study setup);
• Review and verify study data and source documentation for accuracy and completeness;
• Monitor the progress and quality of study activities (both on-site at study centres and remotely via electronic data capture systems);
• Oversee study centres' compliance with study protocols, Good Clinical Practice (GCP) and other research ethics and regulatory requirements, prepare and write monitoring reports;
• Assist in the proper closure of clinical studies;
• Facilitate study audits and inspections as needed; and
• Perform other duties related to clinical trial management as assigned.

Requirements:

• Bachelor's degree or above in Health, Biological/Life Sciences, Medical, Pharmacy, Nursing or related disciplines;
• Experience in clinical research operations and development, and/or basic knowledge in Good Clinical Practice (GCP) are added advantages;
• Good interpersonal and communication skills allowing collaboration with cross-functional teams;
• Good coordination and problem-solving skills, and commitment to quality and compliance;
• Detail-minded, able to handle multiple concurrent tasks, and have a strong sense of responsibility; and
• Good command of written and spoken English and Cantonese (proficiency in Putonghua is a plus).

The appointment will commence as soon as possible on a 1-year temporary basis or 2-year fixed-term basis, with the possibility of renewal subject to satisfactory performance.  A highly competitive salary commensurate with qualifications and experience will be offered, in addition to annual leave and medical benefits.  Appointment on 2-year fixed term basis will attract a contract-end gratuity and University contribution to a retirement benefits scheme, totalling up to 10% of basic salary.

Application Procedure

The University only accepts online application for the above post.  Applicants should apply online at the University's careers site ) and upload an up-to-date C.V.  Review of applications will start from October 9, 2025 and continue until October 25, 2025, or until the post is filled, whichever is earlier.

CRA II/ Senior CRA - office-based in Hong Kong. Join us and advance your career with an industry leading CRO.

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.

We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.

What You Will Be Doing

• Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
• Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
• Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
• Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
• Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile

• Advanced degree in a relevant field such as life sciences, nursing, or medicine.
• Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
• Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
• Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
• Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
• Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver's license

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

Interested 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