Job Opportunities

Director, Statistical Programming

Reports to: Sr. Director, Biostatistics

PMV Pharma is pioneering the development of first-in-class p53 regulators for cancer treatment. By bringing together leaders in the field and leveraging over three decades of p53 biology research, PMV Pharma integrates unique biological insights with a strong focus on pharmaceutical development

Responsibilities:

  • Provide strategic and scientific leadership for integrated safety and efficacy analyses (ISS/ISE) at program and platform levels
  • Lead programming support for global submissions, including integrated datasets, TLFs, define.xml files, and reviewers’ guides
  • Partner with Biostatistics Lead to define and execute a global programming strategy focused on innovation, scalability, and quality
  • Collaborate with clinical development teams to influence analysis planning, interpretation, and data-driven decision-making
  • Oversee global programming operations—including internal teams and partners, to ensure high-quality deliverables and operational consistency
  • Champion advanced technologies such as R, Python, cloud automation, to optimize workflows and enhance efficiency
  • Establish robust programming processes and SOPs for integrated analyses and submissions to ensure standardization and audit readiness
  • Act as a senior escalation point for complex analytical, regulatory, or operational challenges
  • Promote continuous learning, inclusion, collaboration, and professional growth within PMV 
  • Contribute to PMV broader Biostatistics and Data Science innovation agenda by translating scientific insights into robust analytic solutions

Experience and Qualifications:

  • Bachelor’s degree in Statistics, Mathematics, Computer Science or related discipline; advanced degree preferred
  • Programming experience in oncology therapeutic area a must 
  • 18+ years (15+ years with advanced degree) of experience in pharmaceutical/CRO industries with extensive leadership in integrated analysis (ISS/ISE) and global submissions (NDA/BLA/MAA)
  • Comprehensive understanding of FDA/EMA/PMDA regulations including eCTD submissions, define.xml files, reviewers’ guides, CDISC standards (SDTM/ADaM), ISS/ISE requirements
  • Expert knowledge of SAS (Base/Macro/STAT/GRAPH/SQL)
  • Proven track record of strategic oversight at the program level with experience in vendor management and cross-functional collaboration (Biostatistics, Clinical Development, Data Management)
  • Extensive experience leading global teams with strong governance frameworks for vendor partnerships (ex: PPD vendors are working with different standards, so this knowledge is preferred) 

Salary Range & Benefits:

  • The expected salary range for this position is $220,000 to $255,000, representing the potential low and high ends. Actual salaries may vary depending on factors such as experience, skillset, and performance.
  • The salary range listed is just one component of our total compensation package. PMV Pharma also provides a competitive suite of benefits, including, health care benefits (medical, prescription drugs, dental, and vision insurance), paid parental leave benefits and adoption assistance, a generous Paid Time Off program, Employee Stock Purchase Plan, rewards and recognition program and much, much more.

How to Apply

To apply, please submit your cover letter and resume to recruiting@pmvpharma.com or apply through our Online Portal.

PLEASE, NO PHONE CALLS or AGENCIES

PMV Pharmaceuticals is an Equal Opportunity Employer and all applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

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