Locations: Durham, NC; New York, NY; Cambridge, MA; Basel, Switzerland
Compensation: Competitive

We provide exceptional opportunities for ultra-high performing individuals ready for their next challenge. We seek top talent from within the biotechnology industry and beyond the conventional pharmaceutical industry. Dermavant Sciences is forming a diverse team that builds on skill sets and performance norms that are highly valued in other sectors, including finance and technology.

We have several scientific and operational teams across the company that we are looking to grow, including, but not limited to:

  • Clinical development and operations
  • Pre-clinical development
  • Regulatory affairs
  • Commercial operations
  • Legal
  • Business operations

If our entrepreneurial spirit and your expertise align, we invite you to contact us about current openings.

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Location: Durham, NC or New York City
Compensation: Competitive

Our employees are its most important assets. We believe strongly in the importance of building balanced teams, combining those with experience in the biopharmaceutical industry with “natural athletes” who come from other industries - such as finance, consulting and technology - in order to challenge the status quo and shape the future of both our business and the pharmaceutical industry.

The Sr. Director, Biostatistics and Data Management will have overall responsibility and accountability of Biostatistics, Statistical Programming, and Clinical Data Management across the Roivant portfolio through across all stages and aspects of development, including regulatory submissions and due diligence of potential Roivant assets. This individual will engage clinical and project teams across the company’s portfolio, providing subject matter expertise and strategic direction to the Clinical programs. He/She will partner with non-clinical and clinical teams regarding the conduct of experiments, statistical methodology, data analysis and interpretation, and managing regulatory issues. He/She is expected to provide oversight and supervision of relevant external consultants and clinical research organizations, primarily as it relates to external data management, statistical and programming work. In addition, this individual will create, develop, validate and maintain all programs for assigned projects in compliance with standard operating procedures.

We are looking for a top quality individual with the following characteristics:

  • Deeply motivated self-starter with an entrepreneurial spirit
  • Desire to work in a quickly changing, fast-paced environment
  • Unrelenting dedication to delivering results and a desire to shape the strategic goals of the business
  • Ability to overcome ambiguity and challenge the status quo
  • Manage multiple programs with competing and aggressive time lines, prioritize activities, and work independently;
  • Willing to roll up your sleeves to get the job done
  • Requirements for consideration include:
  • A Master’s degree in Statistics, Mathematics, or related field; Ph.D. preferred.
  • Relevant clinical and pharmaceutical industry experience in the planning and conduct of clinical trials, preferably late-stage development experience.
  • 7+ years industry experience in Biostatistics, Statistical Programming and Clinical Data Management, including regulatory interactions and submissions.