Associate Director/Director, CMC Regulatory
Cambridgeonsitedirector$143K – $233K
via Greenhouse
About this role
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.…
What we'd score you on
reqspace match rubricFive dimensions, recruiter-grade. Upload your resume and we'll generate a written explanation of where you fit and where the gaps are.
1
Skills match
For this role: teams
2
Level fit
This role is director-level. We check your trajectory against it.
3
Domain experience
Your work in the role's domain matters more than your years total. We weight recent and direct experience.
4
Recency
A skill you used last quarter weighs more than one from five years ago. We grade on recency, not lifetime.
5
Location fit
This role is based in Cambridge. We weight your proximity and willingness to relocate.
Score yourself on this role.
Free · no card · written explanation included
Skills in this role
Pulled from the job description. These are the keywords we'll weight when scoring your fit.
teams
More at Relaytherapeutics
- View →Senior Manager, Drug SubstanceCambridge, MA
- View →Medical Science Liaison - SoutheastSoutheast
- View →Associate Director, Drug ProductCambridge, MA
- View →Senior Manager/Associate Director, Portfolio & Strategy OperationsCambridge, MA
- View →Senior Manager, Drug ProductCambridge, MA
- View →Senior Manager, Analytical Development & QCCambridge, MA
