Covance

Snr Medical Dir

Job Location(s) CN-Shanghai
Job Number
2021-70263
Job Category
Medical Director
Position Type
Full-Time
Telecommute
No

Job Overview

Reporting to the China Oncology Medical Head, the primary role of the incumbent will serve as a physician providing 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, this role 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.
  
Responsibilities
- Serves as project physician and can serve as a program level physician across multiple indications 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 - Reviews laboratory values, adverse events, coding dictionaries and data tables, listings and figures as needed
- 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 and actively participates in investigator meetings
- Provides medical/scientific expertise to project teams
- Responsible for medical and safety monitoring on assigned projects
- 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
- Provides clinical and medical expertise to other Covance departments
- Contributes to the scientific strategic leadership for a given therapeutic area
- 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 support optimal recruiting and conduct of trials
- Ability to present or serve on panels to represent the company at conferences and scientific meetings
- Therapeutic and Scientific Expertise
- Develops training modules and materials, and provides training in disease states and protocol specific requirements across the Company
- Participates in training opportunities to advance knowledge of drug development and good clinical practice guidelines
- Perform other duties as assigned by management.

Education/Qualifications

-MD degree with specialization in Oncology preferred
-Board Certification history
-Relevant sub specialty fellowship training
-excellent communication and interpersonal skills
-ability to travel globally

Experience

-A minimum of 5 years clinical research experience within a pharma or CRO environment
-Previous experience in medical practice/patient care
-Experience supporting Phase I-IV clinical trails
-strong knowledge and experience with oncology clinical trails

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