Jobs in Massachusetts, Usa
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Global Regulatory Lead
Title: Associate Director Regulatory AffairsA small but growing clinical stage company is seeking an Associate Director Regulatory Affairs to join the team in a remote capacity. They are seeking a well-rounded RA professional to lead the Regulatory Strategy for their pipeline of phase III products in the rare disease space. Responsibilites:Serves a...
Oncology Regional Business Director
Role: Regional Business Director (1st Line People Leadership role)Company Type: Small BiotechRegion: Northeast Area (NY, Central PA, Northern NJ, CT, RI, MA, NH, VT, ME) Company Profile:This biotech is focused within rare oncology and looking to become a leading player in this space as a result; a highly experienced profile is required, with a stro...
Director, Antibody Engineering
Director, Antibody and Protein Engineering Summary of RoleA leading global biopharma is seeking their next Director of Antibody & Protein Engineering. As Director, you'll head a team designing and optimizing antibodies and proteins, driving candidates from discovery to clinical development. You'll integrate advanced computational tools and structur...
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Associate Director, Government Pricing
FeaturedJob Title: Associate Director, Governmenyt PricingLocation: Boston, MA (Hybrid 3x on-site) A reputable, large Pharmaceutical company is seeking a Government Pricing professional for their Market Access business unit. This individual is responsible for all activities relating to the administration and processing of rebates, pricing submissions, cert...
VP of CMC (Biologics)
Vice President of CMC BiologicsHybrid Company Overview:We are partnered with an emerging Biotechnology company focused on developing Best-in-class Therapeutics to address unmet medical needs. This leading Biopharma has several assets across multiple stages of development and are on track to hit multiple milestones H2 of this year. Job Summary:We ar...
Regulatory Affairs Specialist
We have a current opportunity for a Regulatory Affairs Specialist on a contract basis. The Regulatory Affairs Consultant will be responsible for providing strategic guidance on regulatory requirements and submissions for medical devices. This role involves ensuring compliance with global regulations, preparing and managing regulatory submissions, a...