Openings >> Medical Director-Hematology/Oncology-Remote
Medical Director-Hematology/Oncology-Remote
Summary
Title:Medical Director-Hematology/Oncology-Remote
ID:20154672087
Labor Type:Contract
Posting #:AM400005MG
Location:United States
Compensation:Contract
Description
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.

Requirements:
  • 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. 

QUALIFICATIONS 
· MD or DO degree from an accredited medical school and (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
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