Overview

Reference Number: JO-1910-438954
Medical Director – Oncology
Rate: Negotiable
Job Type: Permanent
Location: United States

CPL Physicians is currently working with a Successful, Progressive, Full-service global clinical research organization (CRO) headquartered in Ohio that provides pharmaceutical, biotechnology and medical device companies with a broad range of clinical research services in support of Phase I-IV drug development.

They are seeking a Drug Safety Physician to work as a Medical Director providing clinical safety and medical monitoring to various biotech clients across the US and globally. They work in various therapy areas but primarily oncology, neurology and dermatology.

The company aims to provide a comprehensive suite of pre- and post-authorization services designed to ensure safety while focusing on the rapid approval of a compound and pharmacovigilance monitoring thereafter.

The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of that safety and PV aspects of clinical trials. Additionally, this role acts as the internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report.

Responsibilities
Provide medical management and expertise for clinical trials;
Contribute medical expertise to study reports, regulatory documents, and manuscripts;
Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials;
Participate in new business development through involvement in proposal and sponsor meetings as requested;
Coordinate with other departments in all phases of the studies and trials including feasibility assessments, design processes, educational efforts, management of medical information, and reviewing and editing of medical documents;
Follow specific research related protocol and lead others in strict adherence to the policies.
Qualifications
Must have an M.D. with a demonstrable track record in successful pharmacovigilace provision to clinical trials

We offer:
Generous Base Salary
Lucrative Bonus of up to 30% of your salary
Full Benefits
Stock options
No Nights, Weekends, or Holidays!
Relocation provided

For more information please CLICK APPLY and forward an up to date resume

Upload your CV/resume or any other relevant file. Max. file size: 128 MB.
I would like to be contacted via SMS
I have read and agree to the Clinical Professionals Group Privacy Policy

Find our privacy policy here