US/Global Medical Director/Scientific Director, Hematology, Multiple Myeloma
Core
Provides specialist medical and scientific strategic and operational input into core medical affairs activities, including clinical data generation, safety surveillance, and supporting product strategies for multiple myeloma.
Role type
Senior IC Medical/Scientific Director (Hematology/Multiple Myeloma)
Builds
Clinical trial protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions, and scientifically accurate marketing materials.
Domain
Pharmaceutical industry, Hematology, Multiple Myeloma
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Clinical trial methodology, data analysis and interpretation, regulatory requirements knowledge, development strategy, protocol design, safety monitoring, PI selection, study enrollment oversight, cross-functional leadership, therapeutic area expertise
Preferred skills
Academic or hospital environment experience, post-doctorate experience, due diligence experience, translational strategy design, mentoring and training
Technologies
Clinical trial software, regulatory submission systems, statistical analysis tools
Responsibilities
Initiates medical affairs activities and generates data supporting scientific strategy; oversees conduct of clinical trials and resolves safety issues; screens and drives execution of investigator-initiated studies; provides clinical expertise for multiple myeloma; participates in design of safety and risk management plans; leads delivery of scientific alignment and brand plans; develops innovative research concepts for clinical data generation; drives execution of publication plans; interacts with internal stakeholders and external investigators; ensures budgets, timelines, and compliance are factored into programs.
Seniority
Senior, hands-on IC with leadership responsibilities