Medical Director / Senior Medical Director

137832
  • 250000 USD - 250000 USD
  • , United States
  • Permanent

We partnered up with a cutting-edge bio-pharmaceutical company nestled on the West Coast, passionately committed to pioneering cancer treatment. At our company (whose name remains confidential), we focus on developing innovative therapeutic solutions, including bi-specific and tri-specific antibodies, along with ADC's. Our mission revolves around creating biologics that intervene systematically within solid tumor microenvironments, aiming to directly combat tumors or activate the immune system for tumor elimination.

Role Overview: We're seeking a dynamic individual to lead and drive our clinical development program. As a pivotal part of our team, you'll orchestrate the planning, execution, and interpretation of clinical trials or research activities. Collaborating across diverse functions, you'll play a pivotal role in delivering high-quality clinical data that underpins our scientific and business strategies.

Key Responsibilities:

  • Shape and execute clinical development programs based on robust medical and scientific principles, ensuring compliance with regulatory requirements.
  • Oversee the entire lifecycle of clinical studies, ensuring integrity, safety, and efficacy data are meticulously reviewed and communicated.
  • Take charge of designing, analyzing, and reporting scientific content for various study/program documents, maintaining the highest standards.
  • Proactively monitor trial safety in collaboration with the Safety team, evaluating safety data and addressing related queries.
  • Act as a medical lead within the Clinical Study Team, fostering a comprehensive, cross-functional approach to medical oversight.
  • Engage with opinion leaders, fostering collaborations to enhance our understanding of compounds and disease areas.

Requirements:

  • M.D. or equivalent, with 2+ years (Director level) or 4+ years (Sr Director level) of Oncology clinical trials experience.
  • Proven track record in managing product safety within Oncology clinical trials, preferably with Biologicals (ADCs and Immune Oncology).
  • Expertise in global drug development, risk management plans, and safety interpretation.
  • Advanced analytical, communication, and leadership skills with a sound medical judgment.

Perks and Benefits:

  • Competitive salary range of $210,000 - $300,000 annually based on skills and experience.
  • Comprehensive benefits package covering medical/dental/vision, 401(k) with company match, generous PTO, sick leave, and more.
  • A stable, well-funded environment with ample opportunities for professional growth and learning.

 

Sarah McGraw Division Manager

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