Job Description

Medical Director / Medical Monitor – Hematology & Oncology

Location: Boston, Massachussets

The Opportunity:

An established clinical-stage biopharmaceutical organization is seeking a Medical Director / Medical Monitor with deep experience in hematology-oncology to support the clinical development of late-stage programs.

This role plays a critical part in driving high-quality clinical execution and providing medical leadership across multiple studies.

Role Focus:

The position combines medical monitoring , clinical development support , and regulatory-facing responsibilities , working closely with internal teams and external partners to ensure trials are delivered efficiently, compliantly, and to a high scientific standard.

Core Accountabilities:

• Provide medical leadership for Phase II–III oncology clinical trials , with a primary focus on hematologic indications
• Oversee medical monitoring activities to ensure adherence to protocols, SOPs, GCP, and applicable regulatory requirements
• Support trial design, protocol development, and ongoing study execution in line with international clinical research standards
• Act as a key medical contact for investigators, maintaining regular communication and participating in on-site visits as required
• Partner cross-functionally with clinical operations, regulatory, safety, and external vendors to ensure study milestones are met
• Participate in safety governance activities, including data review and safety committees
• Contribute to the preparation and review of clinical and regulatory documentation, including medical sections of submissions and publications
• Provide medical input across broader development activities such as clinical strategy, scientific review, and portfolio evaluation

Required Background:

• Medical degree ( MD )
• Several years of hands-on experience in hematology-oncology clinical development
• Direct involvement in Phase I–III clinical trials , including medical monitoring and study oversight
• Experience working within a pharmaceutical, biotech, or CRO environment
• Strong understanding of global regulatory frameworks and GCP requirements
• Ability to communicate effectively with investigators, regulators, and cross-functional teams

Additional Details:

• Some flexibility in working hours may be required due to collaboration across time zones
• Limited travel expected (approximately 10%)

If interested, please apply here directly or contact me on the below information for further details:

joel.isaac@vividresourcing.com

+1 (980) 222 2267

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