In search of a physician career change opportunity or a new non-clinical career? An executive search firm is working with a well known pharmaceutical company located in New Jersey, to fill the position of Assistant Vice President Clinical Affairs.
Scope of essential responsibilities:
Responsible for the medical monitoring of multiple clinical trials in all phases of study. Lead cross-functional groups to generate and implement clinical development plans and selected pipeline products. Responsible for design, execution and analysis and reporting of clinical trials both for internal and regulatory uses, including pivotal and activity-finding studies in a variety of oncologic indications.
* Provide medical monitoring for clinical trials.
* Work with biostatistics on trial design and analysis.
* Work with monitoring and contract research organizations on study conduct.
* Adhere to principles of good clinical practice.
* Work with medical writing on reports and presentations.
* Recruit and communicate with investigators.
* Make presentations at internal and external meetings.
* Provide support and advice on safety issues with candidate compounds.
* Work with discovery on relevant experimental designs for new drug candidates.
* Provide strategic input and backup to other development programs and to the drug safety group, and to support the company with external presentations at scientific and commercial meetings.
Qualifications:
M.D. with >5 years experience in oncology. Excellent working knowledge of clinical oncology practice. Thorough familiarity with areas of investigation in relevant tumor types and with the regulatory landscape. Ability to manage various functional groups productively.
Highly competitive remuneration including incentives package.
If you are interested in this position, please email your cover letter and CV/resume to info at prnresource.com and we will send it to the search firm looking to fill this position.
BR 10-26
