Recursion Pharmaceuticals

Recursion Pharmaceuticals

Director, Regulatory Affairs

New York, New York · Director

Sponsorship not specified$228k-$281kDetected 7 days ago
NegotiationRecruitingPharmacologyFDA RegulatoryResearchLeadershipCommunicationCollaborationProblem SolvingRegulatory Affairs

About the role

  • There may be occasional opportunities or expectations for travel to our Salt Lake City headquarters or other office locations.
  • Caring means holding a deep sense of responsibility and respect - showing up, speaking honestly, and taking action. - We learn actively and adapt rapidly.

Responsibilities

  • Participate in global product team meetings; provide regulatory support and guidance and manage day-to-day regulatory activities
  • Manage complex issues and coordinate multiple projects simultaneously in a time-sensitive fashion while practicing sound judgment as it relates to risk assessment (immediate and long term impact on program)
  • Create and follow procedures for regulatory execution and implementation of regulatory strategies while actively supporting program leads via the Clinical Study Teams (CSTs) to deliver on business objectives for assigned products/programs (e.g. clinical trial applications, marketing authorization applications, orphan drug designation applications, pediatric submissions, etc.).
  • Create, collaborate and comply with disclosure and transparency policies for applicable jurisdictions
  • Review and interpret regulatory guidelines and create a communication plan to distribute relevant impact assessment.
  • Creatively think outside the box on how to influence and shape the future of regulatory sciences as it relates to use and validation of unprecedented use of technology to develop drugs effectively for faster paths to patients.
  • Including your own.
  • Recursion is at the forefront of reimagining drug discovery and development through broadening the funnel of potential targets, using technology and standardization to build connected data, and superlinearly scaling our efforts to accelerate the delivery of high-potential drug candidates to the clinic.
  • Collaborate with cross-functional leads to support the development of regulatory strategies and implementation for all jurisdictions as applicable to the program.
  • Plan and perform critical reviews of documents for consistency and quality, and identify gaps in critical documentation in alignment with the regulatory strategy with the intention of achieving successful registration and lifecycle management of unique products.

Requirements

  • Strong understanding of regulatory strategy and implementation of operational activities.
  • Demonstrated proficiency in organizational awareness, including experience working cross-functionally and on global teams

Skills

  • Outstanding management, interpersonal, communication, negotiation, and problem-solving skills.

Compensation

  • Based on the skills, experience, and qualifications needed for this role, the estimated annual base salary range is:
  • New York City, Boston, & San Francisco Bay Area(s): $228,250-$280,720
  • Salt Lake City & all other U.S. locations: $207,500-$255,200
  • In addition to base salary, this role is eligible for an annual bonus, equity compensation, and a comprehensive benefits package.

Benefits

  • A minimum of 10 years in the pharmaceutical industry with a minimum of 8 years in Global Regulatory Affairs, experience with major Health Authority (US FDA, Health Canada, UK MHRA and EMA) is mandatory.
  • Collaborate with strategic operations and other functions (e.g. Clinical, Commercial, Medical Affairs, amongst others) to provide regional regulatory insight for futuristic planning and considerations for the program
  • Serve, as needed, as the point of contact with relevant Health Authorities and/or lead interactions with such authorities or other relevant external stakeholders

Company info

  • Reporting to the Vice President, Regulatory, you'll lead the development of regulatory strategies for assigned programs.
  • You'll work collaboratively with fellow team members and stakeholders from toxicology, pharmacology, and clinical development to support clinical programs (IND-enabling and clinical-stage assets) in alignment with Recursion's regulatory strategy.
  • The Experience You'll Need
  • A minimum of 10 years in the pharmaceutical industry with a minimum of 8 years in Global Regulatory Affairs, experience with major Health Authority (US FDA, Health Canada, UK MHRA and EMA) is mandatory. Oncology, rare disease and I&I is good to have.
  • Minimum of 8 years experience with regulatory submissions (e.g. Investigational New Drug Applications(INDs), New Drug Applications (NDA/NDS/MAA), post marketing measures, Paediatric Investigation Plans (PIP)/(PSP) and Orphan Drug Designation (ODD), Breakthrough Designation (BTD), EU PRIME activities) are mandatory.
  • Strong understanding of regulatory strategy and implementation of operational activities. Outstanding management, interpersonal, communication, negotiation, and problem-solving skills. Demonstrated proficiency in organizational awareness, including experience working cross-functionally and on global teams
  • Working Location & Compensation:
  • This role is remote-friendly, with most work conducted from home.
  • At Recursion, we believe that every employee should be compensated fairly.
  • Based on the skills, experience, and qualifications needed for this role, the estimated annual base salary range is:
  • New York City, Boston, & San Francisco Bay Area(s): $228,250-$280,720
  • Salt Lake City & all other U.S. locations: $207,500-$255,200
  • In addition to base salary, this role is eligible for an annual bonus, equity compensation, and a comprehensive benefits package.

Equal opportunity

  • Recursion is an Equal Opportunity Employer.
Apply directly at Recursion Pharmaceuticals →Create a free account for alerts like thisView Recursion Pharmaceuticals immigration profile

This listing is sourced directly from Recursion Pharmaceuticals's careers page and normalized into a canonical job model.