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in Thousand Oaks, CA

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About this job

This position can be located in either Thousand Oaks, CA, San Francisco, CA, or remote.

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 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.

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




About Aerotek:

We know that a company's success starts with its employees. We also know that an individual's success starts with the right career opportunity. As a Best of Staffing® Client and Talent leader, Aerotek's people-focused approach yields competitive advantage for our clients and rewarding careers for our contract employees. Since 1983, Aerotek has grown to become a leader in recruiting and staffing services. With more than 250 non-franchised offices, Aerotek's 8,000 internal employees serve more than 300,000 contract employees and 18,000 clients every year. Aerotek is an Allegis Group company, the global leader in talent solutions. Learn more at Aerotek.com.

Aerotek is acting as an Employment Agency in relation to this vacancy.