Senior Medical Director

Role Summary

Senior Medical Director, reporting to the Chief Medical Officer, guiding and supporting clinical programs, shaping the clinical development plan for new compounds, co-designing and overseeing clinical studies, and partnering with Program Teams across Research & Development to map the path toward regulatory approval. Collaborate with colleagues across all phases of development, engage with academic investigators and opinion leaders, and represent the company with Health Authorities.

Responsibilities

• Drive development programs, collaborating with Program Management, Clinical Operations, Regulatory Affairs, and cross-functional teams, designing and refining oncology clinical study protocols from first-in-human Phase I through pivotal studies supporting regulatory submissions.
• Serve as a medical monitor for multiple clinical trials in relapsed refractory multiple myeloma, evaluating clinical and laboratory data, guiding recruitment, study conduct, dose escalation, and early signals of activity as appropriate.
• Provide input and leadership in preparing global regulatory filings, including clinical sections of IBs, INDs, CTAs, and NDAs.
• Foster regular engagement with academic clinical investigators, support site initiation visits, and lead investigator meetings to promote collaboration and trust.
• Partner with Pharmacovigilance to review and interpret clinical data, ensuring accuracy, context, and patient safety.
• Represent the company with the scientific community, contribute to publication plans, and build relationships with external experts to inform program strategies.

Qualifications

• Required: A M.D. with experience in adult hematological oncology, plus at least two years of clinical development experience in biotechnology or pharmaceutical settings (or equivalent combination of academic and industry experience).
• Knowledge of drug development from IND through NDA, including experience with companion diagnostics, clinical operations, and pharmacovigilance.
• Experience designing and delivering early- and late-stage programs, proactively addressing challenges and aligning teams toward shared outcomes.
• A flexible contributor who can balance strategic vision with hands-on execution.
• Skilled communicator who listens actively, adapts to diverse audiences, and builds understanding across teams and stakeholders.

Skills

• Medical strategy and program leadership
• Clinical trial design and monitoring
• Regulatory filing readiness and interaction
• Cross-functional collaboration and stakeholder management
• Scientific communication and publication planning

Education

• Medical Degree (M.D.) required.

Additional Requirements

• No additional travel or physical demands were specified as essential in this description.