Medical Director / Medical Monitor – Hematology & Oncology
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.
- 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
- Some flexibility in working hours may be required due to collaboration across time zones
- Limited travel expected (approximately 10%)
If interested, please apply directly or contact me for further details:
Seniority level: Director
Employment type: Full‑time
Job function: Science
Industries: Pharmaceutical Manufacturing
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