Consultant Medical Director / Medical Monitor
Commercial Stage Biotech s is seeking an experienced consultant Medical Director / Medical Monitor to support a late-stage hematology program. This is a hands-on consulting role for a senior physician who can quickly step into an active development program and contribute across medical monitoring, clinical data review, regulatory support, and cross-functional execution.
Engagement Snapshot
Role Type
Consulting / contract
Initial Term
Approximately 6 months, with potential to extend
Start Timing
Near-term start preferred
Therapeutic Area
Hematology; lymphoma expertise strongly preferred
Program Context
Support work related to lymphoma study, including broader medical and regulatory activities connected to the program
Opportunity
- The consultant will provide senior physician-level support for an active hematology development program, with a focus on medical monitoring, clinical/safety data review, study team partnership, and regulatory-readiness activities.
- This role requires a practical, biotech-savvy physician who is comfortable working directly in the data, communicating clearly with cross-functional stakeholders, and helping the team maintain execution discipline in a lean environment.
Key Responsibilities
- Provide medical monitoring support for an ongoing hematology clinical program.
- Review clinical and safety data and partner with the study team on patient-level and aggregate data interpretation.
- Collaborate closely with clinical scientists, clinical operations, biostatistics, safety, regulatory, and medical affairs.
- Contribute medical input to regulatory documents, submission-related materials, and health authority response activities.
- Support clinical content for abstracts, presentations, publications, and other program communications.
- Help evaluate emerging data trends, safety signals, protocol questions, and medically relevant study issues.
- Partner with cross-functional team members to support study execution, data-cleanup activities, and regulatory deliverables.
- Help maintain strong medical oversight, urgency, and execution discipline in a fast-moving biotech environment.
Ideal Background
- MD or equivalent physician training required.
- Significant hematology experience required; lymphoma expertise strongly preferred.
- Prior experience as a medical monitor and/or clinical development physician in biotech or pharma.
- Experience supporting late-stage oncology or hematology clinical programs preferred.
- Comfortable working directly in the details of clinical data, safety review, and study-level medical questions.
- Able to contribute to regulatory and submission-related work, including health authority questions and supporting documentation.
- Able to operate independently, communicate clearly, and work effectively in a lean, cross-functional team.
- Practical, proactive, vocal when needed, and execution-oriented.
Best-Fit Profile
- Experienced hematologist / lymphoma-focused physician who has served as a hands-on medical monitor or clinical development lead.
- Biotech-savvy operator who can quickly orient to an active program and add value without a long ramp.
- Strong clinical judgment, clear communication style, and willingness to engage directly in data review rather than simply providing high-level oversight.
- Collaborative partner to clinical science, operations, safety, regulatory, medical affairs, and biometrics teams.
Consultant Medical Director / Medical Monitor