Similar posts
Regulatory Affairs Lead
- Permanent
- Labelling & Artwork, Operations
- United States
This vacancy has now expired. Please see similar roles below...
Proclinical is currently recruiting for a Regulatory Affairs Lead with a biotechnological company located in Cambridge, MA. The US Regulatory Lead (USRL) is responsible for all aspects of the US Regulatory Strategy for assigned development and marketed products. The USRL is a critical member of the Regulatory Product Team (RPT) providing US focused product strategy, US regulatory framework knowledge, and awareness of external regulatory initiatives. The USRL will present the US regulatory position on assigned products to senior management governance committees as needed.
Job Responsibilities:
- Core member of the RPT collaboratively working with the team to represent the US Business and weave US strategies into global strategies as they are developed.
- US participant on Product Cross Functional Team as appropriate.
- Key contact for FDA on product(s) and with direct FDA interaction. Ensures communications from FDA are properly communicated to the business after assessing the feedback and outlining next steps.
- Key contact for internal research, development and business partners on product(s).
- Drives US product labeling, working with the GRL to ensure core label changes are appropriately conveyed in US product labeling. Partners with US Commercial and Ad Promo Team.
- Responsible for IND, NDA, and BLA submissions to FDA in partners with Regulatory Operations.
- Responsible for product labeling, working with the GRL to ensure core label changes are appropriately conveyed in US product labeling.
- Regulatory representative on due diligence assessments of new business opportunities as required.
- Provide mentorship to junior regulatory staff.
Skills and Requirements:
- 8+ years pharmaceutical industry experience in R&D, Regulatory or related functions, with at least 5 years working in regulatory affairs.
- Delivery of at least one major application (NDA or BLA) or extensive experience with neurology late stage development/marketed products.
- Great leadership skills with high emotional intelligence.
- Must be a great team player with strong verbal and written communication skills.
If you are having difficulty in applying or if you have any questions, please contact Zachary Hines at 215-531-6914.
ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
#LI-ZH1
Related jobs
Highly Competitive Salary
Philadelphia, USA
Proclinical Staffing is seeking an Associate Director of Regulatory Affairs to join a top medical program.
Up to US$290000 per annum + Highly Competitive Salary
Boston, USA
Proclinical Staffing is seeking a Senior Director, Regulatory Affairs to join a leading health information technology and clinical research organization.
Up to US$225000 per annum + Highly Competitive Salary
San Francisco, USA
Proclinical Staffing is seeking a Senior Director, Regulatory Affairs to join a cutting-edge AI company.
Highly Competitive
Luton, England
Proclinical is seeking a meticulous Proofreader for Artwork & Labelling Implementation Management.