Remote Contract Jobs
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C++ Qt Developer
Senior Software Engineer - Modern C++ / QtOverviewWe are supporting an international technology organization developing high-quality desktopsoftware products used in mission-critical environments. The team is growing and is looking for aModern C++ / Qt Software Engineer to join a collaborative, multi-site engineering group.This role sits within a t...
C++ Qt Developer
Senior Software Engineer - Modern C++ / QtOverviewWe are supporting an international technology organization developing high-quality desktopsoftware products used in mission-critical environments. The team is growing and is looking for aModern C++ / Qt Software Engineer to join a collaborative, multi-site engineering group.This role sits within a t...
Sr. Regulatory Affairs Consultant
Contract: 12-month, full time contractStart date: ASAP Client: US based large MedTech Working hours: Supporting US Team, some requirements for availability in CST time zoneJob Description:Assesses regulatory intelligence to assist in the development of local, regional, and global regulatory strategiesParticipates in advocacy activities of a more ad...
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Chief Medical Officer (Part-time)
EPM Scientific are currently partnered with an early-stage clinical biotech which is advancing a programme in haemato-oncology. They are urgently seeking a Chief Medical Officer, reporting to the CEO, to provide hands-on medical leadership and drive their clinical development efforts forward. See a summary of the role below:Role Overview:Start Dat...
Biostatistician (AD Director Level)
EPM Scientific are currently partnered with an innovative Biotechnology company advancing a portfolio of early- and late-phase Oncology programmes. They are urgently seeking a Senior Statistical Consultant / Associate Director (Biostatistics), reporting to the Senior Director Biostatistics, to support their expanding Biometrics team. The role will ...
Freelance Regulatory Writer Medical Devices
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,...