Work Schedule
Other

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.

• 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.

• MD, MB/BS or equivalent degree and strong medical knowledge, validated clinical experience handling Oncology or Neuroscience patients in hospital practice
• Significant experience within pharmaceutical industry, clinical trials or pharmaceutical medicine is beneficial
• Is proficient in spoken and written English
• Solid understanding of regulatory guidelines for adverse event reporting
• Strong communication & presentation skills and is a strong standout colleague

• Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.
• Able to work upright and stationary for typical working hours.
• Able to work in non-traditional work environments.
• Able to use and learn standard office equipment and technology with proficiency.
• Able to perform optimally under pressure while prioritizing and balancing multiple projects or activities.
• May have exposure to potentially hazardous elements typically found in healthcare or laboratory environments.