Skip to content

This website uses cookies to provide features and services. By using the site you agree to the use of cookies.Cookie policy.  Close

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
Click apply
6/11/2021 2:25:26 PM

We strongly recommend that you should never provide your bank account details to an advertiser during the job application process. Should you receive a request of this nature please contact support giving the advertiser's name and job reference.