Regulatory Strategy, Director (Bay Area, Boston)

Premier Research

$150K *
Pharmaceuticals & Biotech
11 - 15 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in science or health-related field; Master's or PhD preferred
  • 12+ years in CRO, pharmaceutical, biotechnology, or device/diagnostics industry
  • 8-9 years progressive regulatory affairs experience with 4+ years as a consultant
  • Experience interacting with FDA, EMA, and other regulatory bodies
  • Leadership in opening INDs and managing NDA/BLA/MAA submissions
  • Expertise in drug development across multiple phases and product types
  • Preferred location: San Francisco or Boston

Responsibilities

  • Develop and execute regulatory program strategies for projects
  • Lead regulatory teams in the US and internationally
  • Implement creative approaches for regulatory success
  • Act as key player in FDA and other regulatory agency interactions
  • Prepare essential submissions including INDs and NDAs/BLAs
  • Serve as primary contact for regulatory agencies on projects

Benefits

  • Comprehensive health insurance
  • Retirement plans
  • Paid time off
Full Job Description
Premier Research is looking for a Regulatory Strategy, Director (Bay Area, Boston) to join our Regulatory Affairs team.

What you'll be doing:
  • Develop and execute regulatory program strategies and contingencies for assigned projects
  • Lead both US and ex-US regulatory teams on assigned projects
  • Develop and implement creative approaches to ensure regulatory success
  • Provide efficient and effective regulatory representation with clients as well as across the organization and act as a key player in interactions with the Food and Drug Administration (FDA) and other regulatory agencies
  • Serve as the primary point of contact and interface for FDA/EMA/national agencies on assigned projects
  • Lead the preparation of submissions, which may include INDs, briefing documents, orphan drug applications, breakthrough designations, and NDAs/BLAs/MAAs and others


What we are searching for:
  • Bachelor's degree, or international equivalent from an accredited institution, in science or health related field; Master's Degree or PhD preferred
  • 12+ years of experience in the CRO, pharmaceutical, biotechnology or device/diagnostics industry; an advanced degree will be considered in lieu of a portion of industry experience
  • 8-9 years progressive regulatory affairs experience (US and/or ex-US) for a CRO/biotech/pharma of which 4+ years has been as a consultant
  • Demonstrated experience interacting with the Food and Drug Administration (FDA), European Medicines Agency (EMA), and other regulatory agencies
  • Demonstrated leadership experience in the opening of INDs and submission and approvals of NDAs/ BLAs/MAAs
  • Expert in the drug development process with experience in multiple phases (early and late stage, post-approval) in various therapeutic areas and product types (drugs, biologics, drug-drug combinations, drug-device combination products)
  • Preferred Location: San Francisco or Boston


Premier Research is dedicated to providing compensation that is fair and competitive with market standards. The annualized minimum base pay for this role is $150,000.00 USD. The actual salary will be influenced based on a variety of factors such as the candidate's qualifications, skills, competencies, and proficiency for the role. We also offer a comprehensive benefits package, which may include health insurance, retirement plans, and paid time off.

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