Jobs in Usa
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AD Human Resources for Mid-sized Pharmaceutical Company
Associate Director, Human Resources Business PartnerOncology | Neurology | Medical AffairsGreater NY Area, Hyrid$160,000 - $210,000 base salary + benefits packageCompany OverviewA mid-sized pharmaceutical company focused on developing and commercializing innovative therapies is seeking an experienced Human Resources leader to join its growing organ...
Chemical Process Engineer
About the OpportunityOur client is a specialized engineering and development organization supporting complex chemical manufacturing and process innovation programs across a variety of highly regulated industries. They are seeking a Process Engineer to join a multidisciplinary team focused on process development, scale-up, optimization, and technolo...
Medical Writer / Senior Medical Writer Med Affairs/Promo Med Ed
Senior Medical Writer / Medical WriterBoston, MA (Hybrid)EPM Scientific is partnering with an award-winning, independently owned medical communications agency that is growing its scientific services team. We're seeking both Medical Writers and Senior Medical Writers to join a collaborative, science-first organization known for delivering high-impac...
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Senior Director of Quality
Role: Sr. Director of Quality Location: Minneapolis, MN (On-site) Salary: $185k - $250kEPM is partnering with an innovative cardiovascular medical device company developing next-generation technologies designed to improve patient outcomes in structural heart, cardiac rhythm management, and interventional cardiology. As the organization continues to...
Clinical Trial Manager
Clinical Trial ManagerJoin a clinical-stage biotech at an exciting stage of growth, where you'll take ownership of complex clinical programs and work directly with senior leadership to help bring innovative therapies to patients with significant unmet needs.What You'll DoLead global clinical trials from start-up through closeoutOversee CROs, vendor...
Head of Regulatory
Head of Regulatory Affairs (Senior Director/VP) Location: San Mateo, CA (Hybrid, 3 days a week in office)About the Company My client is a specialty biotech company with an approved rare disease product and an active Phase 3 program. The company handles regulatory strategy and writing in-house, which gives this role broad ownership and direct involv...