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Clinical Trial Managaer Remote (USA) $70-$90 per hour Job DescriptionEPM is partnered with a cutting-edge biotech that is dedicated to pioneering breakthrough therapies for diverse and traditionally unmet medical needs related to liver diseases. Their mission? To revolutionize healthcare and the way that patients are treated across the globe. With ...
Validation Engineer
This position is responsible for supporting the validation and quality engineering of various systems in a medical device manufacturing environment and assure the equipment/system and validation records are compliant with company standards and industry practices.Work requires originality and judgment in the independent evaluation, selection, and su...
Site Relationship Manager Contractor (m/f/d)
EPM Scientific is currently working with US Biotech who are seeking a Freelance Site Relationship Manager for their Rare disease pipeline who lives close to Chicago (ORD), Minneapolis (MSP) or Detroit (DTW), or alternatively to Dallas (DFW), Houston (IAH) as it's a travel intense role. The role will require you to act as a local liaison between th...
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Site Relationship Manager
EPM Scientific is currently working with US Biotech who are seeking a Freelance Site Relationship Manager for their Rare disease pipeline who lives close to Dallas (DFW), Houston (IAH), or alternatively to Chicago (ORD), Minneapolis (MSP) or Detroit (DTW) as it's a travel intense role. The role will require you to act as a local liaison between the...
Freelance Site Relationship Manager
EPM Scientific are currently partnered with a clinical-stage immunology biotech, urgently seeking a Freelance Site Relationship Manager to join their team. See a short summary below: Contract Conditions:Start date: ASAPLocation: Dallas-Fort Worth/Houston, TexasContract Type: Freelance / Consultant - 0.7 FTE, 12 MonthsLanguage: English essentialProj...
Medical Writer Regulatory
U.S.-based medical device company at the final stages of our clinical program and preparing for a 510(k) submission. We are seeking an experienced Medical Writer with a strong background in regulatory writing for medical devices, specifically 510(k) and/or De Novo submissions. This is a contract role requiring full-time availability for the next co...