Openings >> Medical Director-Hematology/Oncology-Remote
Medical Director-Hematology/Oncology-Remote
Title:Medical Director-Hematology/Oncology-Remote
Labor Type:Contract
Posting #:AM400005MG
Location:United States
Location: Candidate has the option to work remote if not in Thousand Oaks or San Francisco, CA

3 Year Contract 
Please on submit if qualified 

NO CORP to CORP, H1 or candidates needing sponsors

This is an opportunity with a top pharmaceutical company in an exciting work environment.

  • Oncology experience
  • Medical Monitoring
  • Clinical development
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. 

· MD or DO degree from an accredited medical school and (2) years of clinical research and/or basic science research experience 

· 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
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