Associate Medical Director (China)
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Job Location:
Monthly Salary:
Posted on:
Yesterday
Vacancies:
1 Vacancy
Job Summary
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 well invite you for an interview. If youre 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.
Job Overview:
Provide medical safety expertise directly and indirectly to Sponsors undertaking clinical trials of drugs devices and combination products and in the post marketing period; and may manage a team.
Summary of Responsibilities:
- Responsible for medical review of serious adverse events and adverse events of special interest from Clinical Trials in support of safety activities for clients.
- Develops new and enhances existing client relationships whenever possible.
- Provides medical/safety expertise to colleagues within PSS and A including communicating information regarding safety regulations and any changes that have occurred.
- When applicable responsible for preparation and medical review of Aggregate Reports (such as Periodic Adverse Drug Experience Reports PADERs) required by global regulatory agencies for review of safety information for assigned products.
- Provides safety support/expertise to project physicians as appropriate.
- Presents Safety capabilities to clients as part of a proposal team when appropriate.
- When applicable responsible for medical review of serious adverse events and non-serious adverse events from spontaneous reports and reports derived from regulatory authorities and the medical literature during post marketing surveillance in support of safety activities.
- When applicable responsible for signal detection and evaluation activities and preparation and submission of Ad Hoc Reports reviewing specific safety issues to the global regulatory agencies for assigned products.
- All other duties as needed or assigned.
Qualifications (Minimum Required):
- MD or DO with at least one year of postgraduate training or equivalent having substantial knowledge of drug / device safety and the underpinning global regulations.
- Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
Experience (Minimum Required):
- At least 4 years of experience working for a pharmaceutical company health authority or a contract research organization in Safety or related fields such as QA Regulatory Affairs medical writing or clinical medical monitoring.
Preferred Qualifications Include:
- MD who has completed an accredited residency program or equivalent and is board-eligible or certified with at least 4 years experience.
Physical Demands/Work Environment:
- Office Environment or remote.
- Travel is primarily Regional for client meetings with 5% of the time and with 75% of that time requiring an overnight stay.
Learn more about our EEO & Accommodations request here.
Required Experience:
Director
Key Skills
- EMR Systems
- Post Residency Experience
- Occupational Health Experience
- Clinical Research
- Managed Care
- Primary Care Experience
- Medical Management
- Utilization Management
- Clinical Development
- Clinical Trials
- Leadership Experience
- Medicare
