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Principal Reg Specialist
san francisco$125,000 - $150,000 USD a year

Influence Regulatory Strategy for Products That Reach Global MarketsThe OpportunityA global medical device manufacturer is looking for a Regulatory Affairs Specialist to join a well-established regulatory team supporting a diverse product portfolio.This is a role for someone who wants to move beyond transactional regulatory work and become a valued...

Clinical Contract Associate (m/f/d)
BerlinNegotiable

EPM Scientific is partnering with an innovative medical device company looking to hire a Clinical Contract Associate to manage DACH across cardiovascular devices. Key Requirements:Strong background in medical device clinical research within cardiovascularProven experience managing end-to-end European clinical trials and external vendors (CROs, labs...

Senior C++ Developer Medical Imaging
RemoteNegotiable

Senior Software Engineer - C++ / Medical ImagingLocation: Remote (Europe)Contract Type: Freelance / ContractIndustry: Medical TechnologyOverviewWe are partnering with a global medical technology organisation developing advanced imaging systems used within highly regulated healthcare environments.They are seeking an experienced Senior Software Engin...

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Selby Jennings Start Your Career In Recruitment
Senior C++ Developer
FreiburgNegotiable

Senior C++ Software Engineer (MedTech) - Contract | Germany | Long-Term ProjectWe're supporting a leading medical device company on a long-term software development programme focused on improving and modernising an existing, market-released product.The successful engineer will work within a mature codebase, identifying technical limitations, refa...

Freelance Regulatory Writer Medical Devices
Negotiable

OverviewWe are supporting a leading medical device organisation seeking an experienced Freelance Regulatory Writer - Medical Devices with strong FDA submissions expertise to support ongoing regulatory documentation activities across the device portfolio.Key ResponsibilitiesAuthor, review, and finalise FDA submissions including 510(k), De Novo, PMA,...

Clinical Supply Chain Planner
BerlinNegotiable

Freelance Clinical Supply Chain Planner (Remote - Europe)Location: Remote (Europe-based)Contract: Freelance / ContractDuration: 9-12 monthsOverviewA leading pharmaceutical/biotech organisation is looking for an experienced Freelance Clinical Supply Chain Planner to support a growing portfolio of clinical trials. This is a fully remote role offering...