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What this posting tells you
Senior Medical Director role at PPD Pharmaceutical Development in China, fully remote with option for office or home-based. Responsible for medical support of clinical trials and safety evaluation in the Pharmacovigilance department. Requires medical monitoring, safety data analysis, and regulatory submission expertise. Schedule is standard Mon-Fri office hours. Employment types include contract and full-time.
Data, Healthcare admin, Marketing, Product, Sales, Customer support
China
Asia/Shanghai
Senior · contract · full_time
- Compensation is not listed
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Explore the remote job marketSenior Medical Director at 91110101799951519A PPD Pharmaceutical Development (Beijing) Co, Ltd
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
Due to continued growth, CRG is now looking to appoint an Associate Medical Director/Medical Director of Neuroscience, to join our team of Medical Directors in China. This role can be office-based or home based.
The Associate Medical Director/Medical Director will be responsible for providing medical support and medical advice for clinical trials and safety evaluation within the PPD Pharmacovigilance department.
A day in the Life
- Provide study, project and program-specific medical monitoring and review services, including but not restricted to:
- Leading of all medical aspects of contracted tasks. Supervising of safety variables.
- Discussing with clients, investigators and healthcare professionals of medical issues in the pre and post approval services by using accurate medical judgment, interpretation and decision.
- Provide medical consultation to team members and answer study related medical questions. Communicate clearly with associates and clients, maintaining and open line of communication to ensure all procedures are followed appropriately
- Analysis and assessment of safety data to identify and run emerging safety signals.
- Medical review of individual case safety reports, serious adverse event reports and clinical outcome reports.
- Assist in Business Development activities
- Present PPD standard medical safety processes to clients at business development meetings and connect with various medical communities to explore and expand PPD business.
- Participate in training of project teams.
- Provide therapeutic and protocol training as needed.
- Write, review and approve reports, regulatory submissions and protocols, ensuring that the medical content is accurate and complete.