at Labcorp in Dover, Delaware, United States
Job Description
Job Overview:
Reporting to the Executive Medical Director, the primary role of the Senior Medical Director / Medical Director will be to serve as a physician providing medical delivery services and subject matter and drug development expertise. He/She will be expected to be a key contributor to the medical strategy and execution of clinical programs. Furthermore, the Senior Medical Director / Medical Director will play a key role in people leadership/management, client relations, and business development representing Labcorp Drug Development in proposals and industry meetings as needed. This is a remote home-based role with travel (US and Global) as needed.
Responsibilities to include;
Client Relationship & Business Development Activities
+ 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 support 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 Labcorp Drug Development 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 leadership for the Oncology programs
Education/Qualifications:
+ Doctor of Medicine
+ BE/BC in Oncology and/or Hematology preferred
Experience:
+ Experience with medical monitoring of Oncology clinical trials
+ Previous experience within the CRO or Pharmaceutical/Biotech industry
+ History of trial work with focus in head / neck squamous cell carcinomas a plus, but not required