Associate Director/Manager, Field Medical Affairs

Dendreon Corporation•Seal Beach, CA

3h•Hybrid

About The Position

The Associate Director/Manager, Field Medical Affairs is a key member of Dendreon’s Medical Affairs leadership team and serves as a player-coach, providing national leadership for the U.S. Medical Science Liaison (MSL) team while maintaining direct field responsibilities across the Western United States (WA, AK, OR, ID, MT, WY, CO, ND, SD, NE, KS, CA, NV, UT, AZ, NM, HI). This role is responsible for ensuring consistent execution of medical strategy, maintaining scientific and compliance excellence, and fostering cross-functional collaboration with clinical, commercial, and regulatory partners. The position leads initiatives that drive scientific exchange, insight generation, evidence dissemination, and investigator support, contributing to Dendreon’s mission to advance innovative immunotherapies for prostate cancer. NOTE:This is a field-based role supporting the Western U.S. region, with up to 60% travel. When not in the field, the position is expected to be based out of our Seal Beach, CA office and is not a fully remote role. Candidates should reside within a commutable distance to Seal Beach, CA, or be willing to relocate.

Requirements

Advanced scientific or clinical degree required (PharmD, PhD, MD, DO, DNP or equivalent).
Minimum 10+ years of related experience in the pharmaceutical, biopharmaceutical, or life sciences industry.
Minimum 5 years of experience as an MSL, including 3+ years in a leadership or mentoring role (team lead, regional director, or equivalent).
Demonstrated success leading medical teams and executing national field strategies.
Proven record of scientific credibility and thought leader engagement in oncology, immuno-oncology, or related therapeutic areas.
Strong strategic thinking, decision-making, and organizational leadership skills.
Minimum 5+ years of related experience in the pharmaceutical, biopharmaceutical, or life sciences industry.
Minimum 3 years of experience as an MSL, including 1+ years in an established leadership capacity (team lead, regional MSL manager, or direct people management)
Proven ability to lead, mentor, and develop medical staff and drive execution of medical strategies.
Demonstrated proficiency in medical engagement, clinical research support, and cross-functional collaboration.
Strong communication and analytical skills with a focus on scientific accuracy and compliance.

Nice To Haves

Prior experience in cellular therapy or immunotherapy (prostate cancer experience preferred).
Established relationships with oncology or urology Key Opinion Leaders (KOLs).
Experience supporting Investigator-Initiated Trials (IITs) and clinical development programs.
Familiarity with eQMS, CRM, and insight management systems.
Proven ability to manage multiple priorities and deliver results in a matrixed environment.

Responsibilities

Lead, coach, and develop the U.S. Medical Science Liaison (MSL) team to ensure consistent execution of medical strategy, compliance with company policies, and excellence in scientific engagement.
Provide direction on field medical strategy and operational objectives aligned with corporate and departmental goals.
Serve as a senior member of the Medical Affairs leadership team, contributing to strategic planning, performance tracking, and resource allocation.
Support development of medical affairs plans, annual goals, and budget forecasts.
Maintain personal field responsibility for KOL and HCP engagement within the Western U.S. region.
Establish and strengthen peer-to-peer scientific relationships with thought leaders in oncology, urology, and immuno-oncology.
Deliver accurate, balanced, and compliant scientific information to external stakeholders.
Gather, analyze, and communicate field medical insights to inform strategy, evidence generation, and business planning.
Represent Dendreon Medical Affairs at national and regional medical congresses, advisory boards, and scientific meetings.
Partner with Clinical Operations to identify investigators, support site qualification, and enhance clinical trial execution.
Collaborate with Medical Communications, Regulatory Affairs, Pharmacovigilance, and Market Access to ensure alignment and compliance.
Support Investigator-Initiated Trial (IIT) programs, including proposal review and progress tracking.
Contribute to development of scientific content and internal training materials.
Ensure that all activities are conducted in accordance with company SOPs, regulatory standards, and industry guidelines (PhRMA Code, OIG, FDA, etc.).
Monitor and report MSL performance metrics and field activity outcomes.
Drive continuous improvement across medical field operations, leveraging technology, analytics, and process optimization.
Report monthly team activities using dashboard-based metric system.
Other duties as assigned.