Sr. Medical Director, Safety Evaluation & Risk Management

Bothell, Washington State (US)
Competitive salary and benefits
Apr 22, 2018
Jun 22, 2018
Medical Director
Full Time

<p>Seattle Genetics is passionate about making a positive impact on the lives of patients with cancer. Employees bring that enthusiasm to everything they do, striving to attain their individual goals while recognizing the power of working collaboratively to realize Seattle Genetics' vision of improving patient outcomes. View this career recruitment video to learn about Seattle Genetics' culture and hear directly from chemists, clinical researchers and sales professionals. As a company working at -- and advancing -- the cutting edge of antibody-based therapies, Seattle Genetics fosters an environment that recognizes the challenges of breaking new ground and creates opportunities for intellectual and professional growth. State-of-the art facility gives our team members the resources to succeed. Located in Bothell's Canyon Park area, Seattle Genetics is close to major highways, dining and shopping. If you are passionate about bringing the best of yourself to everything you do, Seattle Genetics offers challenges, opportunities and rewards for making your best even better. We want to hear from you!</p>

Sr. Medical Director, Safety Evaluation & Risk Management


The Medical Director/ Sr. Medical Director SERM will be responsible for strategic medical leadership for global pharmacovigilance and risk management activities for assigned Seattle Genetics, Inc. investigational and marketed products. 

This individual will serve as a member of the Drug Safety leadership team and function in a company matrix team environment interacting with several key internal stakeholder groups including; Clinical Affairs, Medical Affairs, Regulatory Affairs, Quality Assurance, Commercial, Translational & Experimental Medicine and Legal. 


  • Provide oversight for members of the Safety Evaluation and Risk Management (SERM) group in Drug Safety
  • Represent Drug Safety in Clinical Sub Team for assigned investigational products providing expert medical guidance regarding safety matters and issues
  • Lead Safety Management Team for assigned pre-marketing and/or post-marketing product(s) and all associated risk management activities
  • Participate in the Signal Management System with regular review of safety data for assigned products for identification and evaluation of new safety signals
  • Perform/provide oversight for medical review of individual safety reports from clinical trials or post-marketing sources
  • Contribute to preparation and review of periodic reports (PADER; PSUR; Annual IND report; 6-monthly line-listings; EU Annual Safety Report; DSUR)
  • Participate in protocol development to ensure alignment with risk management plans
  • Review and provide medical content, as needed, for key study-related documents, e.g. IB, ICF, SMC/IDMC Charters
  • Contribute to analysis of safety data from on-going and completed clinical trials and presentation in Clinical Study Reports
  • Facilitate production and maintenance of risk management plans and safety communication (marketing applications, company core safety information, regulatory safety queries, etc.) to regulatory agencies or third parties
  • Participate in continuous improvement activities including systems design, performance measurement and quality management
  • Provide guidance and mentorship to staff on pharmacovigilance and risk management best practices and safety science
  • Provide input to Pharmacovigilance agreements and interactions
  • Participate in alliance safety teams with external partner(s)


  • MD (board certified or ex-US equivalent)
  • Minimum of 3 years (Director) or 5 years (Sr Dir) in Drug Safety, Clinical Safety, Pharmacovigilance or Risk Management
  • Oncology safety science experience preferred
  • Knowledge of ICH, US & EU regulations and requirements for pharmacovigilance (experience with world-wide safety reporting regulations and guidelines required)
  • Excellent interpersonal skills, including ability to work effectively cross culturally and cross functionally
  • Excellent written and spoken English
  • Prior experience with business partners a plus

Seattle Genetics is an equal opportunity employer. All qualified applications will receive consideration for employment without regard to race, color, religion, sex, national origin, protected veteran status, or disability status.

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