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Freelance Clinical Research Associate
EPM Scientific is currently partnering with a leading Cardiovascular Medical Device company that is seeking an experienced Clinical Research Associate Contractor on a remote basis. Key Requirements: Proven experience as a CRA within the cardiovascular medical device field.Strong knowledge of FDA regulations and GCP guidelines.Hands-on experience wi...
Freelance Senior Business Anayst (Supply Chain)
We are partnering with a leading, global Medical Device client of ours here at EPM Scientific who are actively looking for a Freelance Senior Business Analyst - Data Sciences (Supply Chain) to join their organisation on a long term assignment in California.Location: Southern California (Hybrid - 3/4 days onsite)Duration: 12 months, Full TimeDepartm...
Regulatory Affairs Associate
Associate/Senior Associate, Regulatory AffairsLocation: San Carlos, CA (Hybrid options available) Industry: Clinical-stage BiopharmaceuticalsA leading clinical-stage biopharmaceutical company is seeking a talented Associate or Senior Associate in Regulatory Affairs to join their growing team. This organization is focused on developing innovative th...
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Quality Engineer Validation
Position: Quality EngineerLocation: Asheboro, NC - OnsiteEmployment Type: W2 onlyContract Length: 6 Months with permanent extensionRole SummaryThe Quality Engineer will play a key role in validating and launching new parts and components, ensuring the quality of medical products, and managing quality control and assurance processes. This position i...
Consultant Senior Clinical Project Manager
EPM Scientific are currently partnered with a Pharmaceutical company who are seeking a Consultant Senior Clinical Project Manager to support their existing Hepatology programs. See a short summary below: Contract Conditions:Start date: ASAPLocation: United States (Remote)Contract: 0.8 - 1 FTE, 12-Month ContractLanguage: EnglishProject: Hepatology -...
CSV Consultant
Please note: Applicants must hold an EU passport or existing right to work in the EU (no sponsorship available). Fluency in French or Dutch is mandatory.A leading pharmaceutical/biotech organisation is seeking an experienced Computer System Validation (CSV) Consultant to support critical projects in compliance with GAMP 5 guidelines. This role offe...