Vice President, Asset Management

This clinical-stage biotech company utilizes a proprietary platform to develop precision therapeutics for cancers and other diseases. They are seeking a Vice President of Regulatory Affairs to develop and lead global regulatory strategies for their portfolio of programs and serve as the primary contact with health authorities. This is the first FTE regulatory hire for this company and this role initially will be an individual contributor position with consultancy support. This company offers innovative science, a collaborative company culture, and flexible work arrangements. Build and lead the Regulatory Affairs function, ensuring adherence to regulatory standards and requirements for the company. Develop and lead global regulatory strategies for a portfolio of oncology programs. Serve as primary contact with FDA and other regulatory agencies, leading all communications and meetings. Provide key updates and guidance on Regulatory activities to Executive Team and Board of Directors as needed. Play a core role in project teams, developing global regulatory strategies for drug development programs, including clinical and pre-clinical stage programs. Coordinate and manage regulatory submissions (e.G. INDs, clinical trial applications, marketing applications) in collaboration with multi-disciplinary development teams as well as senior management. Contribute to the creation of the overall product development strategy and manage the development, monitoring, and delivery of Regulatory project plans throughout the life cycle. Provide input on development plans, Target Product Profile (TPP) development, risk assessments, resource planning, and other documents as required. Lead regulatory meeting preparation efforts supported by the program team. Ensure on-time, high-quality and regulatory–compliant submissions. Liaise with regulatory publishing and other ancillary regulatory functions at CROs and consultants to coordinate regulatory submissions. Build key infrastructure for Regulatory to support the development, approval, and launch of products. Train others on regulatory requirements as needed. Develop and maintain partnerships and networks to support delivery of regulatory goals. Bachelors in a scientific discipline required. MS, MD PharmD, or PhD) preferred. A minimum of 10 years of Regulatory Affairs experience in the biopharmaceutical industry. Must have strong Regulatory experience with oncology programs. Experience supporting both early and mid-phase development, including development and filing of associated regulatory submissions. A track record of successful interaction with FDA and other regulatory agencies. EMA, Ex-US or global regulatory experience required. Some experience with CMC Regulatory a plus. Experience with alternative regulatory pathways (e.G. breakthrough designation, priority review, fast track) strongly preferred. Must be an experienced, hands-on-problem-solver who can develop a broad vision for a unique regulatory strategy while supporting ongoing activities on a day to day basis. Ability to review, understand and explain the regulations and guidance documents to guide project teams. In-depth understanding of the drug development, product commercialization and life cycle management processes. Strong track record working with program teams to advance development assets is essential. Previous Regulatory team leadership desired. This is a hybrid position in the Greater Boston Area. Local candidates in the Boston Area will be onsite 3 days a week. Candidates outside of the Boston area will be expected to be in the office at least one week per month. The budgeted salary range for this position is $300,000 to $350,000 plus an annual target bonus, equity, and comprehensive benefits. Posted salary ranges do not include incentive compensation or any other type of renumeration. #