Associate Director

As part of the Pharmaceutical Development team, this position will play a key role in regulatory strategy development and execution of assigned Chemistry, Manufacturing and Control (CMC) programs.   

Your Role: 

• With minimal supervision, accountable for developing and leading the execution of regulatory CMC investigational, registration and/or post-approval strategies for Relay's development programs/products.
• Develop and execute CMC global submission plans and timelines in accordance with project goals
• Strong and deep foundational understanding of global RA CMC regulations and guidelines.
• Apply and adapt this understanding to projects to enhance probability of regulatory success and regulatory compliance.
• Ability to draw from prior experience, precedents and other regulatory intelligence beyond regulations.  Strong analytical or process understanding that enables the development of robust and accurate submissions.
• Apply global regulatory CMC knowledge to address and overcome challenges that arise during development and commercialization.
• Responsible for leading and coordination of responses to CMC questions/RFIs from regulatory authorities in conjunction with CMC and regulatory affairs leads/SMEs.
• Independently defines CMC content (data and documentation) requirements for regulatory submissions and reviews this content for conformance with established requirements.
• Responsible for CMC-regulatory activities listed above with cross-functional teams and act as the regulatory CMC liaison between CMC/PD, regulatory affairs and/or program management, as applicable.
• Lead and manage CMC-regulatory assessment and guidance on product compliance topics, including change controls, deviations, and GMP investigations, as applicable, in conjunction and consultation with CMC leadership.
• Proactively communicates CMC regulatory strategies, key issues and risks through assigned programs / products development activities and LCM in adequate and timely manner to cross-functional programs/ products teams and management level within PharmDev and Regulatory Affairs Teams, as appropriate.
• Keep abreast of regulatory guidance and technical/scientific developments relevant to projects.

Competencies:

• Strong background in CMC-regulatory affairs with focus on small molecule (preferably solid orals: tablets, capsules) clinical (IND/IMPD) and/or commercial (NDA/MAA) submissions.
• Proven ability to lead and manage regulatory CMC projects independently. Able to deal with issues of critical importance with minimal supervision. Exercises good judgement in elevating and communicating actual or potential issues to line management.
• In-depth knowledge of global CMC regulatory requirements and guidelines (e.g. FDA, EMA, ICH).