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San Francisco, CA Full Time Posted by: Covance Posted: Friday, 11 June 2021
 
 
Job Overview: The primary role of the Medical Director/Senior Medical Director will be to serve as a physician providing medical delivery services and subject matter and drug development expertise. The incumbent will be expected to be a key contributor to the medical strategy and execution of clinical programs. Furthermore, the (Senior) Medical Director will play a key role in people leadership/management, client relations, and business development representing Covance in proposals and industry meetings as needed. This is a remote home-based role with travel (US and Global) as needed. Client Relationship & Business Development Activities + Partnering with GCO to develop new and enhance existing client relationships where possible + Provides leadership and presents medical/scientific capabilities to clients as a participant of a proposal team + Leverage known and builds new relationships with investigators/sites to performs site/investigator feasibility and to s upport optimal recruiting and conduct of trials + Able to present or serve on panels to represent the company at conferences and scientific meetings. Therapeutic and Scientific Expertise + Responsible for medical and safety monitoring on assigned projects + Develops training modules and materials, and provides training in disease states and protocol specific requirements + Participates in training opportunities to advance knowledge of drug development and good clinical practice guidelines + Serve as global lead project physician and provides clinical and medical expertise + May serve as a program level physician across multiple studies for a given company + Provides subject matter and drug development expertise to be a key contributor to the medical strategy and execution of the program for the client + Performs medical data review and/or oversight of central medical data review- laboratory values, adverse events, coding dictionaries and data tables, listings and figures as needed, holistic and aggregated data review + Develops, reviews and revises protocols, case report forms, training materials, project specific tools, analysis plans design, clinical trial reports and new drug applications + Prepares materials for investigator meetings + Actively participates in investigator meetings + Provides medical/scientific expertise to project teams and to other Covance departments + Interacts with inter - departmental and external consultants as appropriate + Participates in feasibility discussions relating to specific project proposals + Participates in project risk assessment activities + Assists when needed with data safety monitoring board activities + Contributes to the scientific strategic l eadership Education/Qualifications: + Doctor of Medicine + BE/BC in Oncology/Hematology preferred Experience: + 5+ years of experience with medical monitoring of Oncology clinical trials or equivalent + History with early phase work preferred + Previous clinical trials experience within the CRO or Pharmaceutical/Biotech industry preferred + Academic experience can be substituted Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran/Sexual Orientation/Gender Identity). Your confidentiality and privacy are important to us.

San Francisco, CA, United States of America
Healthcare
Covance
Click apply
JS11167_1609152646
6/11/2021 2:25:26 PM


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