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Medical Director - Oncology HOME BASED (Science & Biotech)
ANYWHERE USA or CANADA, NY 10021
Recruited by: Sheryl Horowitz | Owner | F-O-R-T-U-N-E Personnel Consultants, Inc. See all my Jobs

  • Hiring Company: F-O-R-T-U-N-E Personnel Consultants, Inc.
  • Industry: Science & Biotech
  • Compensation: Salary
  • Expires: Nov 07, 2019
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Job Description

We are currently looking for a Medical Director/ Senior Medical Director specializing in Oncology to join our client's global Medical Affairs team. We are open to Oncologists (board certified US or foreign board certified) who are interested in moving their career into industry, helping to develop and bring out new drugs for cancer patients. These positions are home-based with minimal travel, and can be based in either the US or Canada.

Working in a fast-paced, client-focused global environment, our Medical Directors play a pivotal role on our client's project teams and with the company. Your medical expertise will be called upon throughout the entire life cycle of a project including partnering with global Business Development for requests for information and attending bid defense meetings for future clinical trials.

Our client provides an expansive global network of resources necessary to help the most people possible. Medical Directors are granted the opportunity to take their experience and expertise farther than ever before, while never losing sight of the ultimate goal - improving the lives of real patients in the real world.

Responsibilities
The Tasks will Include:

Providing input into the creation of the protocol and other study-related documents
Participating in discussions with regulators, key opinion leaders, senior management and clients
Delivering training to external project teams and colleagues
Reviewing medical data on the indication, inclusion / exclusion criteria and other medical issues to ensure overall project deliverables are achieved
Sharing your vast medical expertise at investigator meetings, kick-off meetings, and client face-to-face meetings
Working closely with Drug Safety teams to evaluate Serious Adverse Events and to develop Safety Management Plans, Pharmacovigilance Plans and Risk Management Plans
Maintaining a strong consultative relationship with the client throughout the project life cycle
Medical Monitoring