Sr. Medical Director / Medical Director Job in New Jersey (NJ), Career, Full Time Jobs in Covance, Inc. a division of LabCorp®
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Sr. Medical Director / Medical Director job in Princeton

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Covance, Inc. a division of LabCorp® jobs
New Jersey (NJ), Princeton
Job Code:  2018-22959
Employer:  Covance, Inc. a division of LabCorp®
Job Type:  Full Time

Location
Country:  United States
State:  New Jersey (NJ)
City:  Princeton
10/10/2018

Description
Job Overview
Reporting to the Executive Medical Director - Oncology, the primary role of the incumbent will be to 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, the Sr. 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 up to 40% global travel.

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 Education/Qualifications
- MD degree
- Specialization in Oncology with specialty fellowship training is highly desired
- History of Board Certification Experience
- Minimum of 5 years experience in the clinical research industry as a Medical Monitor
- Experience in and specialization in Oncology is highly desired
- Substantial knowledge of drug development and extensive clinical research experience within the pharmaceutical/CRO industry supporting Phase I - IV clinical trials
ref: (2018-22959)
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