(Snr) Medical Dir - Oncology

Job Location(s) SG-Singapore | MY | PH-Manila | HK | TW-Taipei City
Job Number
Job Category
Medical Director
Position Type

Job Overview

Essential Job Duties:
Company Focus
- Contributes to the development of Company policies involving medical, safety and therapeutics
- Participates in process improvement activities across Company
- Performs other duties as assigned
Client Relationship & Business Development Activities
- Partnering with GCO to develop new and enhance existing client relationships where possible
- Presents medical/scientific capabilities to clients as a participant of a proposal team
- Performs site/investigator feasibility, builds relationships with investigators to support optimal recruiting and conduct of trials 
- Supports and participates in the recruitment process for department positions
- Provides leadership to junior staff within the therapeutic area
- Participates and leads initiatives that serves the physicians within the TA
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
- Serves as global lead project physician
- 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 for investigator meetings
- 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


Minimum Required
- MD Degree
- Relevant sub specialty fellowship training and history of board certification


- At least 3-5 years’ experience with substantial knowledge of drug development and extensive clinical research experience within the pharmaceutical/CRO industry in a specific therapeutic area


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