Dynamic pharmaceutical companies located in the Northern California area are in search of the following professionals with strong oncology backgrounds.
Clinical Oncology Professionals from Director to Sr. Director and Higher levels
Abilities:
Establish and communicate clinical trial strategies for high-quality early clinical decision making directed at highest value labels. Design, prepare and initiate study protocols and other required documentation in compliance with project plans, federal regulations, GCP and good medical practice.
* Work within the project team structure to help evaluate development candidate molecules.
* Supervise both directly and indirectly through a dotted line structure or via other subordinate supervisors.
* Provide guidance, where required, and oversee the activities of other lower level personnel.
* Develop, influence and maintain relationships in the medical community with significant key opinion leaders.
* Research and select investigators.
* Analyze and interpret study data and prepare reports for FDA and publication.
Academic and Empirical background:
M.D. degree with 3 to 5+ years experience in a responsible position focused on oncology clinical development/research. Hands-on experience in the design and execution of controlled clinical trials, with an emphasis on early clinical development. Understanding of basic science relevant to clinical oncology (biochemistry, molecular biology and/or genetics is desirable). Ability to develop, influence and maintain relationships in the oncology community with significant key opinion leaders.
Highly competitive remuneration including base salary, benefits, incentives and overall package plus relocation.
If you are interested in these positions, please send your CV by email to info (at) PRNResource.com, and we will pass it to the recruiter.
