8 Medical Advisor jobs in Hong Kong

Join to apply for the Medical Advisor role at Merck Healthcare

Join to apply for the Medical Advisor role at Merck Healthcare

Work Your Magic with us!
Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.
Key Responsibilities

• Develop and maintain peer-to-peer collaborations and relationships with key medical experts in local medical community
• Support clinical development initiatives including site identification, trial recruitment, registry, and presentation of final approved data
• Collaborate with physicians on medical affairs initiatives including publications, advisory boards, medical education opportunities, training, and speaker development
• Serve as scientific peer-to-peer resource to external disease experts and internal stakeholders
• Support the medical community with up-to-date medical information, robust disease expertise, and product information
• Communicate clinical insights on new data to the company Medical Affairs and to inform medical strategy for the therapeutic area
• Train internal stakeholders on key scientific and medical topics in relevant therapeutic area
• Develop an understanding of the regional landscape including specialties involved in care of patients
• Maintain effective and appropriate communication among internal stakeholders while maintaining full compliance with relevant requirements
• Generate tactical regional plans to provide needs based, value-added support of the medical and scientific community in-line with company goals
• Uses systems to strategically map, identify, profile and prioritize thought leaders in line with the medical plan and goals
• Maintain accurate reporting and documentation of MSL activities
  

• Master degree in biology, pharmacy, or other medical related discipline. Advanced degree preferred, such as MD, PhD, Pharm D, etc.
• 1- or 2-years biotech company related job experience preferred.
• Open for fresh graduate.
  

• Seniority level Associate

• Employment type Full-time

• Job function Research and Science
• Industries Pharmaceutical Manufacturing

Referrals increase your chances of interviewing at Merck Healthcare by 2x

Wan Chai District, Hong Kong SAR 1 year ago

Wan Chai District, Hong Kong SAR 7 hours ago

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Join to apply for the Senior Medical Advisor/ Medical Advisor (Oncology) role at AstraZeneca

3 days ago Be among the first 25 applicants

Join to apply for the Senior Medical Advisor/ Medical Advisor (Oncology) role at AstraZeneca

Do you have expertise in, and passion for providing medical and scientific support? Would you like to apply your expertise to impact the lives of patients in a company that follows the science and turns ideas into life changing medicines? Then AstraZeneca might be the one for you!

About Astrazeneca

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines for some of the world’s most serious diseases. But we’re more than one of the world’s leading pharmaceutical companies. We are on a journey to bring life-saving medicines to patients. Our role in contributing to decreasing mortality rates globally is clear – shaping the future by spotting a scientifically-led commercial opportunity and acting now to operationalise and scale it.

BUSINESS AREA – Hong Kong

Welcome to Hong Kong, one of over 400 sites here at AstraZeneca, providing a collaborative environment where everyone feels comfortable and able to be themselves is at the core of AstraZeneca’s priorities, it’s important to us that you bring your full self to work every day. To help you maintain your best self, here’s a sneak peek into some of the things this site provides for you

• Flexible Medical Benefit for you to better take care of well-being of yourself and your family
• Bright and vibrant work environment
• Top up employer MPF contribution
  
  

• Build, enhance and maintain the engagement with scientific leaders, principally key external experts
• Develop or initiate strategic scientific programs – through scientific meetings, advisory boards, clinical studies and publications – to address or explore unmet medical needs in a specific therapeutic area
• Provide and discuss scientific information and data regarding new launched products to healthcare professionals to ensure quality and accuracy of key medical and scientific information on new treatment options by face to face visits
• Collaborate closely with MSL and Diagnostic team to align external scientific communication
• Provide proactive, updated and effective medical input to internal stakeholders during the pre-launch, peri-launch and post-launch phase of a brand as part of its life cycle management
• Strategic input for overall medical activities and evidence generation plan with budget control
• Ensure overall adherence to internal and external processes and regulations
  
  

• University graduate in science or related discipline
• Preferably 2 years' experience in medical affairs in pharmaceutical industry, with oncology experience is an added advantage
• Competent in Adverse Drug Reaction reporting in compliance with local regulations
• Possess a high ethical standard and knowledge of the HKAPI Code of Practices
• Knowledge of good clinical practice
• Sound computer skills on Microsoft Office
• Excellent in both written and spoken English and Chinese, conversable Mandarin is an advantage
• Excellent analytical, organization and communication skills
• Excellent project prioritization and management skills
  
  

• Experience in Oncology medical affairs in pharmaceutical industry
• Possess PhD/MD/PharmD, or master degree in related discipline; Hong Kong Registered Pharmacist License
• Sound computer skills on Microsoft Office
• Depending on candidate experience, this position may be filled at the following levels: Senior Medical Advisor/ Medical Advisor
  
  

• Are you already imagining yourself joining our team? Good, because we can’t wait to hear from you.
• Are you ready to bring new ideas and fresh thinking to the table? Brilliant! We have one seat available and we hope it’s yours.
  
  

• Seniority level Mid-Senior level

• Employment type Full-time

• Job function Health Care Provider
• Industries Pharmaceutical Manufacturing

Referrals increase your chances of interviewing at AstraZeneca by 2x

Sha Tin District, Hong Kong SAR HK$35,000.00-HK$42,000.00 1 week ago

We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.

Join to apply for the Senior Medical Advisor/ Medical Advisor (Oncology) role at AstraZeneca

3 days ago Be among the first 25 applicants

Join to apply for the Senior Medical Advisor/ Medical Advisor (Oncology) role at AstraZeneca

Do you have expertise in, and passion for providing medical and scientific support? Would you like to apply your expertise to impact the lives of patients in a company that follows the science and turns ideas into life changing medicines? Then AstraZeneca might be the one for you!
About Astrazeneca
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines for some of the world’s most serious diseases. But we’re more than one of the world’s leading pharmaceutical companies. We are on a journey to bring life-saving medicines to patients. Our role in contributing to decreasing mortality rates globally is clear – shaping the future by spotting a scientifically-led commercial opportunity and acting now to operationalise and scale it.
BUSINESS AREA – Hong Kong
Welcome to Hong Kong, one of over 400 sites here at AstraZeneca, providing a collaborative environment where everyone feels comfortable and able to be themselves is at the core of AstraZeneca’s priorities, it’s important to us that you bring your full self to work every day. To help you maintain your best self, here’s a sneak peek into some of the things this site provides for you

• Flexible Medical Benefit for you to better take care of well-being of yourself and your family
• Bright and vibrant work environment
• Top up employer MPF contribution
  

• Build, enhance and maintain the engagement with scientific leaders, principally key external experts
• Develop or initiate strategic scientific programs – through scientific meetings, advisory boards, clinical studies and publications – to address or explore unmet medical needs in a specific therapeutic area
• Provide and discuss scientific information and data regarding new launched products to healthcare professionals to ensure quality and accuracy of key medical and scientific information on new treatment options by face to face visits
• Collaborate closely with MSL and Diagnostic team to align external scientific communication
• Provide proactive, updated and effective medical input to internal stakeholders during the pre-launch, peri-launch and post-launch phase of a brand as part of its life cycle management
• Strategic input for overall medical activities and evidence generation plan with budget control
• Ensure overall adherence to internal and external processes and regulations
  

• University graduate in science or related discipline
• Preferably 2 years' experience in medical affairs in pharmaceutical industry, with oncology experience is an added advantage
• Competent in Adverse Drug Reaction reporting in compliance with local regulations
• Possess a high ethical standard and knowledge of the HKAPI Code of Practices
• Knowledge of good clinical practice
• Sound computer skills on Microsoft Office
• Excellent in both written and spoken English and Chinese, conversable Mandarin is an advantage
• Excellent analytical, organization and communication skills
• Excellent project prioritization and management skills
  

• Experience in Oncology medical affairs in pharmaceutical industry
• Possess PhD/MD/PharmD, or master degree in related discipline; Hong Kong Registered Pharmacist License
• Sound computer skills on Microsoft Office
• Depending on candidate experience, this position may be filled at the following levels: Senior Medical Advisor/ Medical Advisor
  

• Are you already imagining yourself joining our team? Good, because we can’t wait to hear from you.
• Are you ready to bring new ideas and fresh thinking to the table? Brilliant! We have one seat available and we hope it’s yours.
  

• Seniority level Mid-Senior level

• Employment type Full-time

• Job function Health Care Provider
• Industries Pharmaceutical Manufacturing

Referrals increase your chances of interviewing at AstraZeneca by 2x

Sha Tin District, Hong Kong SAR HK$35,000.00-HK$42,000.00 1 week ago

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Join to apply for the Medical Advisor – New Products & Development role at Novartis Hong Kong

4 days ago Be among the first 25 applicants

Join to apply for the Medical Advisor – New Products & Development role at Novartis Hong Kong

Get AI-powered advice on this job and more exclusive features.

Summary

The MA – NP&Dev, is responsible for supporting the design, implementation and execution of Medical Affairs plans for new products within Greater Bay Area (GBA); building strategies including real-world data generation on innovative medicines listed within GBA following GBA policies and communication guidance allowed

Summary

The MA – NP&Dev, is responsible for supporting the design, implementation and execution of Medical Affairs plans for new products within Greater Bay Area (GBA); building strategies including real-world data generation on innovative medicines listed within GBA following GBA policies and communication guidance allowed

About The Role

Key responsibilities:

Medical Affairs strategy in line with global strategy

• Leverage insights from GBA unmet need and treatment landscape to implement planned Medical Affairs activities on assigned products in GBA
• Identify and build strategies for new HK/Macau approved products (not approved in China) to be listed in GBA hospitals
• Build strategies for new product development aligning with local strategies within GBA and HK
  
  

• Execute integrated evidence generation plans to address unmet needs in GBA and HK for new product development
• Execution/oversight on clinical trial or clinical research related activities, including real-world data generation
• Coordinate scientific meeting and educational programs; develop strategic engagement plans
• Report AE/PC within 24 hours of receipt as appropriate
  
  

• Acts as internal subject expert to provide medical insights to cross-functional teams
• Working with GBA cross-functional teams to build GBA strategy
• Coordinate review and approval of locally developed materials and global materials tailored to local needs adhering to ERC, P3 and GBA policies and communication guidance
• Responsible for risk identification and assessment, mitigation planning; implementation and monitoring of appropriate internal controls
  
  

• Coach and manage 2 GBA MSLs based in China
• Ensure timely execution of planned Medical Affairs activities by MSLs in an efficient and compliant way
• Ensure medical enquiries are responded to in a high quality and timely manner compliantly by MSLs
• Oversight and manage GBA MSLs’ responsibilities in a timely manner (iSEC, customer relationship management tool etc.)
  
  

• MD, PharmD, pharmacist, PhD, Master above degree in medical or other life sciences
• Fluent in spoken and written Chinese and English
• Strategic & collaborative mindset across boundaries
• Medical Advisor and new launch experience preferred
• Experience in clinical research and real-world data generation is preferred, but not mandatory
• Experience in project and operation management and execution
  
  

• Seniority level Mid-Senior level

• Employment type Full-time

• Job function Health Care Provider
• Industries Pharmaceutical Manufacturing

Referrals increase your chances of interviewing at Novartis Hong Kong by 2x

Get notified about new Medical Advisor jobs in Hong Kong, Hong Kong SAR .

Wan Chai District, Hong Kong SAR 1 week ago

Sha Tin District, Hong Kong SAR HK$35,000.00-HK$42,000.00 1 day ago

We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.

Join to apply for the Medical Advisor – New Products & Development role at Novartis Hong Kong

4 days ago Be among the first 25 applicants

Join to apply for the Medical Advisor – New Products & Development role at Novartis Hong Kong

Get AI-powered advice on this job and more exclusive features.

Summary
The MA – NP&Dev, is responsible for supporting the design, implementation and execution of Medical Affairs plans for new products within Greater Bay Area (GBA); building strategies including real-world data generation on innovative medicines listed within GBA following GBA policies and communication guidance allowed

Summary
The MA – NP&Dev, is responsible for supporting the design, implementation and execution of Medical Affairs plans for new products within Greater Bay Area (GBA); building strategies including real-world data generation on innovative medicines listed within GBA following GBA policies and communication guidance allowed
About The Role
Key responsibilities:
Medical Affairs strategy in line with global strategy

• Leverage insights from GBA unmet need and treatment landscape to implement planned Medical Affairs activities on assigned products in GBA
• Identify and build strategies for new HK/Macau approved products (not approved in China) to be listed in GBA hospitals
• Build strategies for new product development aligning with local strategies within GBA and HK
  

• Execute integrated evidence generation plans to address unmet needs in GBA and HK for new product development
• Execution/oversight on clinical trial or clinical research related activities, including real-world data generation
• Coordinate scientific meeting and educational programs; develop strategic engagement plans
• Report AE/PC within 24 hours of receipt as appropriate
  

• Acts as internal subject expert to provide medical insights to cross-functional teams
• Working with GBA cross-functional teams to build GBA strategy
• Coordinate review and approval of locally developed materials and global materials tailored to local needs adhering to ERC, P3 and GBA policies and communication guidance
• Responsible for risk identification and assessment, mitigation planning; implementation and monitoring of appropriate internal controls
  

• Coach and manage 2 GBA MSLs based in China
• Ensure timely execution of planned Medical Affairs activities by MSLs in an efficient and compliant way
• Ensure medical enquiries are responded to in a high quality and timely manner compliantly by MSLs
• Oversight and manage GBA MSLs’ responsibilities in a timely manner (iSEC, customer relationship management tool etc.)
  

• MD, PharmD, pharmacist, PhD, Master above degree in medical or other life sciences
• Fluent in spoken and written Chinese and English
• Strategic & collaborative mindset across boundaries
• Medical Advisor and new launch experience preferred
• Experience in clinical research and real-world data generation is preferred, but not mandatory
• Experience in project and operation management and execution
  

• Seniority level Mid-Senior level

• Employment type Full-time

• Job function Health Care Provider
• Industries Pharmaceutical Manufacturing

Referrals increase your chances of interviewing at Novartis Hong Kong by 2x

Get notified about new Medical Advisor jobs in Hong Kong, Hong Kong SAR .

Wan Chai District, Hong Kong SAR 1 week ago

Sha Tin District, Hong Kong SAR HK$35,000.00-HK$42,000.00 1 day ago

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Join to apply for the REGULATORY AFFAIRS MANAGER / RA MANAGER – medical device manufacturer (Kwai Fong/5 days) role at JPC Corporation

6 days ago Be among the first 25 applicants

Join to apply for the REGULATORY AFFAIRS MANAGER / RA MANAGER – medical device manufacturer (Kwai Fong/5 days) role at JPC Corporation

Get AI-powered advice on this job and more exclusive features.

Company Description

Hong Kong - Shenzhen - Guangzhou - Shanghai - Beijing

JPC Texson Ltd, established since 1990, is a Hong Kong and China licensed Employment Consulting firm, specializes in Headhunting and Recruiting Services for companies in Hong Kong and China. We have offices in Hong Kong, Shenzhen, Guangzhou, Shanghai and Beijing.

Job Description

THE COMPANY :

• Medical device & medical instrument manufacturer
• Factories : 2 X production plants in Dongguan
• Sales Offices : Europe and the United States.
• Main market : North America and Europe
• We are looking for REGULATORY AFFAIRS MANAGER - with details as follows :
  
  

• Lead one of the Regulatory teams in Dongguan
• Handle regulatory affairs, such as product license registration/renewal, coordinating customers/internal audits, preparing of ISO documentations and etc.
• Maintain the COPs in comply with ISO 13485.
• Maintain good relationship with certify bodies
• Conduct and organize seminar or training for staff to fulfill the regulatory requirements.
• Report to Plant Director
• Degree holder
• An advantage if studies in Bio Engineering or related
• 3+ year solid experience in medical or pharmaceutical industry or related
• Good knowledge in some of these : ISO 13485, ISO9001, 510K, CE, CMDCAS, CFDA legislation.
• Proficient of English and Mandarin
• Work location : 70-80% Dongguan; 20-30% Hong Kong
• Company shuttle bus provided between Dongguan Changping railway station to Dongguan factory
• 5 days work
• Annual leave : 14 days
• Medical insurance
• Work-life balance culture
  
  

• Seniority level Mid-Senior level

• Employment type Full-time

• Job function Other, Manufacturing, and Product Management
• Industries Medical Practices, Pharmaceutical Manufacturing, and Medical Equipment Manufacturing

Referrals increase your chances of interviewing at JPC Corporation by 2x

Get notified about new Regulatory Affairs Manager jobs in Hong Kong SAR .

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Join to apply for the REGULATORY AFFAIRS MANAGER / RA MANAGER – medical device manufacturer (Kwai Fong/5 days) role at JPC Corporation

6 days ago Be among the first 25 applicants

Join to apply for the REGULATORY AFFAIRS MANAGER / RA MANAGER – medical device manufacturer (Kwai Fong/5 days) role at JPC Corporation

Get AI-powered advice on this job and more exclusive features.

Company Description
Hong Kong - Shenzhen - Guangzhou - Shanghai - Beijing
JPC Texson Ltd, established since 1990, is a Hong Kong and China licensed Employment Consulting firm, specializes in Headhunting and Recruiting Services for companies in Hong Kong and China. We have offices in Hong Kong, Shenzhen, Guangzhou, Shanghai and Beijing.
Job Description
THE COMPANY :

• Medical device & medical instrument manufacturer
• Factories : 2 X production plants in Dongguan
• Sales Offices : Europe and the United States.
• Main market : North America and Europe
• We are looking for REGULATORY AFFAIRS MANAGER - with details as follows :
  

• Lead one of the Regulatory teams in Dongguan
• Handle regulatory affairs, such as product license registration/renewal, coordinating customers/internal audits, preparing of ISO documentations and etc.
• Maintain the COPs in comply with ISO 13485.
• Maintain good relationship with certify bodies
• Conduct and organize seminar or training for staff to fulfill the regulatory requirements.
• Report to Plant Director
• Degree holder
• An advantage if studies in Bio Engineering or related
• 3+ year solid experience in medical or pharmaceutical industry or related
• Good knowledge in some of these : ISO 13485, ISO9001, 510K, CE, CMDCAS, CFDA legislation.
• Proficient of English and Mandarin
• Work location : 70-80% Dongguan; 20-30% Hong Kong
• Company shuttle bus provided between Dongguan Changping railway station to Dongguan factory
• 5 days work
• Annual leave : 14 days
• Medical insurance
• Work-life balance culture
  

• Seniority level Mid-Senior level

• Employment type Full-time

• Job function Other, Manufacturing, and Product Management
• Industries Medical Practices, Pharmaceutical Manufacturing, and Medical Equipment Manufacturing

Referrals increase your chances of interviewing at JPC Corporation by 2x

Get notified about new Regulatory Affairs Manager jobs in Hong Kong SAR .

We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.