Sr. Medical Director

Are you passionate about advancing oncology therapies and making a meaningful impact on patient care? This is a fantastic opportunity to join a leading organization supporting the development of innovative cancer treatments. You will have the chance to work with a dynamic team, influence clinical strategies, and play a crucial role in bringing new oncology solutions to patients worldwide—all while growing your career within a forward-thinking company that values scientific excellence and collaboration.

Our client is a biotech company dedicated to the discovery and development of cutting-edge oncology medicines. They are committed to transforming cancer treatment through innovative research and collaboration. The role of Senior Medical Director is central to their clinical development efforts, focusing on guiding and overseeing the clinical aspects of their oncology pipeline. This position offers the opportunity to lead and shape critical clinical programs, ensuring scientific rigor and patient safety are at the forefront of all initiatives.

Role Summary:
As a Senior Medical Director, you will support the clinical development of oncology programs by providing medical expertise across trial design, execution, and oversight. You will serve as a Medical Monitor, contribute to regulatory interactions, and collaborate closely with cross-functional teams to drive clinical strategy. This role involves working predominantly on-site in Cambridge, MA, with an emphasis on ensuring the successful conduct of clinical trials that impact the future of cancer treatments.

Key Responsibilities:

• Support the design and execution of oncology clinical trials, ensuring alignment with scientific and regulatory standards.
• Serve as Medical Monitor, overseeing patient safety, protocol adherence, and medical data review.
• Collaborate with regulatory affairs, clinical operations, pharmacovigilance, and other teams to optimize trial performance across multiple time zones.
• Represent the organization in interactions with investigators, key opinion leaders, and regulators.
• Analyze clinical data and real-world evidence, identifying trends and informing decision-making to advance clinical development.
• Contribute to regulatory submissions, health authority meetings, and risk management planning.
• Support business development activities, including licensing and partnership evaluations.
• Stay current with oncology trends, regulatory updates, and scientific literature to inform strategy.

Experience & Requirements:

• MD with board certification in Oncology, Hematology-Oncology, or a related specialty.
• Experience in clinical development, particularly late-stage trials, ideally in a Medical Monitor role.
• Strong understanding of oncology drug development, clinical endpoints, and regulatory pathways.
• Proven ability to work effectively in cross-functional teams and communicate complex scientific information clearly.
• High ethical standards with a commitment to scientific rigor.

Salary:
This role offers a base salary between $300,000 and $340,000, depending on experience.

Apply now to be part of a growing team shaping the future of cancer treatment through innovative clinical development.