Senior/Medical Director, Oncology

JOB DESCRIPTION

The role of Senior/Medical Director, Oncology will report to the Vice President of Clinical Development and work collaboratively with the clinical team towards the development and execution of Volastra’s oncology programs. The role will oversee one or more of Volastra’s clinical trials to ensure successful planning, execution and analysis.  The ideal candidate works collaboratively and leads by example, is detail-oriented and self-motivated, and has highly relevant experience in oncology clinical development. 

Volastra is a fast-paced biotech company of passionate employees, and there is ample opportunity for the ideal candidate to grow and develop with the organization. Individuals will from time to time have the opportunity to gain experience with projects outside their direct scope of work. 
 
Job is based in NYC and requires weekly in office presence, 2-3 days per week

RESPONSIBILITIES

• Work collaboratively with the entire clinical organization to drive the strategy and execution of the overall clinical development plans of the company.
• Support the design of clinical trials and contribute to writing medically important documents such as protocols, regulatory documents, and study reports.
• With support from clinical science and consultant/CRO partners, provide medical oversight of clinical trials, including medical monitoring, review of important safety events, and appropriate communications with investigators.
• Build and maintain strong relationships with clinical study investigators and other external partners.
• Work closely with translational sciences to ensure successful clinical biomarker plans for assigned clinical studies.
• Ensure compliance with SOPs, GCP, safety reporting, and other applicable regulations
• Travel to critical medical conferences (<10% travel) 

REQUIREMENTS

• MD, MD/PhD, or equivalent degree, Board Eligible or Certified in Medical Oncology.
• 1+ year of industry experience in a medical monitor/medical director role overseeing oncology clinical program(s).  Additional experience running clinical trials as clinical site study investigator is highly preferred. 
• Understanding of the drug development process from target identification to marketing authorization.
• Strong knowledge of ICH, GCP guidelines, and relevant regulatory requirements.
• Excellent written/verbal communication, organizational, and problem-solving skills.

SALARY RANGE

Base salary approximately $225,000- $305,000 which may vary depending on qualifications, experience, and ultimate leveling. Leveling outside of Senior Director may be considered for exceptional candidates on a case by case basis.