Medical Director-Sr Medical Director, Clinical ...

Medical Director / Senior Medical Director, Clinical Development Seattle, WA | United States Our client is a fast-growing and dynamic organization seeking a Medical Director / Sr Medical Director to join its Clinical Development team. The Medical Director / Sr Medical Director will play a key role at all stages of clinical development. The successful candidate will have oversight for planning and execution of clinical trials and be involved in the exploration of novel indications. The role will provide clinical leadership to cross-functional project teams on development strategies, clinical study outlines and protocols. Compilation and interpretation of study results and interfacing with multiple cross-functional areas including clinical operations, safety, medical and scientific communications, commercial (marketing, sales, managed markets), regulatory, product manufacturing and supply will be key responsibilities, as well as communication and interpretation with external partners, clinical investigators and Key Opinion Leaders. Company Overview Our Client is an innovative biotechnology company focused on discovering, developing, and commercializing small-molecule and biologic therapeutics centered on immune-mediated disorders, hematologic conditions, oncology, and neurobehavioral diseases. Our Client's lead lectin pathway inhibitor has just been approved by the FDA for the treatment of hematopoietic stem cell transplant-associated thrombotic microangiopathy (TA-TMA) in adult and pediatric patients ages two years and older, with a planned U.S. launch in January 2026. The European Launch is in the works. Our Client has also entered license agreement negotiations with Novo Nordisk for an additional inhibitor which will provide a significant strategic partnership and cash infusion. Our Client continues to have a strong financial outlook. Key Role Responsibilities Develop and refine clinical development strategies across multiple therapeutic programs Serve as Clinical Lead on cross-functional project teams Translate strategy into detailed clinical study outlines and protocols Provide ongoing medical monitoring for clinical trials (eligibility, safety surveillance, toxicity management) Collaborate closely with global investigators and research sites Contribute to preparation and review of regulatory submissions, including INDs, safety reports, investigator brochures, and development plans Participate in regulatory interactions and represent the clinical program before health authorities Engage external key opinion leaders to explore novel indications and development pathways Ensure compliance with regulatory requirements and Good Clinical Practice standards Lead data review, analysis, and interpretation for internal and external stakeholders Contribute to scientific publications and presentations Serve as an internal clinical and scientific resource across research, translational science, safety, regulatory, and program management functions Support evaluation of business development opportunities Provide scientific/medical review support as needed Education and Experience MD required; hematology specialization and clinical experience preferred Significant biotechnology or pharmaceutical industry experience Strong strategic thinking and systems-based problem-solving capabilities Excellent written and verbal communication skills Demonstrated leadership and cross-functional collaboration experience Ability to operate effectively in a fast-paced, evolving environment Behavioral Competencies Strategic mindset with strong prioritization skills Ability to influence and collaborate across functions and senior leadership High level of integrity and professional credibility Strong interpersonal and conflict resolution skills Analytical decision-making capability Innovative and forward-thinking approach Additional Information 10-20% travel required (medical congresses, investigator meetings, etc.) Supervisory responsibilities may include hiring, coaching, performance management, and team development Compensation & Benefits Our Client offers a competitive total rewards package, including base salary commensurate with experience, annual incentive eligibility, equity participation, comprehensive health benefits, retirement plan with company match, paid time off, and holidays.

Created: 2026-04-15