Previous Job
Medical Director
Ref No.: 18-03543
Location: Thousand Oaks, California
Position Type:Scientific (T)
Start Date / End Date: 03/12/2018 to 03/11/2021
Our client, a leading fortune company is looking for Medical Director for a 3 years contract position and is located in Thousand Oaks, CA.

Top Skill Sets:
  • Oncology experience
  • Medical Monitoring
  • Clinical development
Ideal Candidate-
  • MD or DO from accredited medical school, 2 years of clinical research and/or basic science research experience.
  • The Medical Sciences/Early Development Group is looking for a Medical Director in Hematology/Oncology. This role will contribute to early phase clinical development of oncology compounds from first-in-man studies through proof of concept. The main role will be focused on Medical monitoring of Early Development clinical trials and contributions to the preparation and conduct of clinical trials.
  • They define, design, and execute early phase clinical and translational projects. They provide subject matter expertise in clinical and translational trial science.
  • This role will include the following responsibilities:
  • Serve as medical monitor for clinical trials and assists in resolving major issues that may affect the studies.
  • Serve as a clinical expert in translational and clinical oncology.
  • Present information internally and externally.
  • Coordinate clinical approaches to operational issues and assign monitoring and safety reporting resources.
  • Provide guidance and assistance in the identification and management of oncology phase 1 collaborators, consultants, and/or Clinical Research Organizations (CROs) in completion of key projects.
  • This position can be located in either Thousand Oaks, CA, San Francisco, CA, or remote.
Basic Qualifications:
  • MD or DO degree from an accredited medical school AND
  • Two (2) years of clinical research and/or basic science research experience
Preferred Qualifications:
  • Subspecialty board eligibility/certification in Oncology and/or Hematology
  • Medical Monitoring Expertise
  • Science or clinical research background in academia or industry
  • Prior experience authoring, monitoring, analyzing, and presenting oncology clinical trials
  • Effective presentation and communication abilities (both written and oral)
  • Ability to anticipate problems and find creative solutions
  • In-depth understanding of the scientific method and clinical applications based on medical, scientific and practical rationale including working knowledge of biomarker methods and clinical imaging endpoints
  • Experience functioning as a medical expert in a complex matrixed environment
  • Previous experience in early phase development and/or biomarker work
  • Previous experience in late stage oncology clinical trials and regulatory filings
  • Demonstrated expertise in conducting translational and/or clinical oncology research.
  • Expertise in Spotfire or other data analysis tools
  • Knowledge of GCP, EMA, and FDA policies
  • Expertise in authoring clinical sections of CTA or INDs
Qualified candidates please send your word format updated resume at the earliest to , Thank You!