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Associate Director, Safety Sciences

Olema Oncology
Full-time
Remote friendly (Boston, MA)
United States
$195,000 - $210,000 USD yearly
Medical Affairs

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Role Summary

Associate Director, Safety Sciences β€šΓ„Γ¬ Safety science expert supporting development of Olemaβ€šΓ„Γ΄s products, collaborating with cross-functional teams and external partners. Based in San Francisco or Boston with less than 10% travel.

Responsibilities

  • Conduct signal detection activities and analyses of safety data to support appropriate benefit-risk assessment
  • Perform signal evaluation for identified safety signal and author safety evaluation reports
  • Manage preparation and completion of safety documents, including DSURs, PADERs/PBRERs, RMPs, and safety sections of protocols, reference safety information for IBs, ICFs, briefing books, NDA, and CCDS, etc.
  • Participate/lead responses to regulatory inquiries and other risk management activities
  • Support clinical/medical review of SAEs, AESI, SUSARs, and AOSE, including reviewing source documents, case narratives, MedDRA coding, queries, expectedness, sponsor assessment, and assisting Safety Operations
  • Conduct literature search activities and develop key strings for search criteria and review information
  • Support and attend Data Monitoring Committee meetings, as required
  • Support quality systems, inspection readiness, audit, and inspections
  • Actively participate in process improvement initiatives and SOP maintenance
  • Collaborate with cross-functional teams and external stakeholders, including business partners and safety vendors/contractors
  • Lead and facilitate safety team meetings with effective communication
  • Apply FDA, EU, and ICH guidelines governing pharmacovigilance activities

Qualifications

  • Required: MD, PhD in medical/biological science, PharmD, or RN; Small Molecule and Oncology experience
  • Experience: 5+ years (MD/PhD/PharmD) or 8+ years (RN) in pharmacovigilance/drug safety in biopharmaceuticals; process improvement and SOP/document support; ability to apply FDA/EU/ICH guidelines; experience with business partners and safety vendors; experience with safety database/clinical database/EDC; mentoring/junior team experience
  • Attributes: strong time management, communication, analytical, problem-solving, strategic planning, interpersonal skills; self-motivated, fast learner; sound judgment and professionalism

Education

  • MD, PhD in medical/biological sciences, PharmD, or RN degree

Additional Requirements

  • No explicit travel beyond less than 10% required
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