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Clinical Research Physician
SydneyNegotiable

Our client is a global biopharmaceutical organization and they are looking for a Clinical Research Physician to support late‑phase clinical programs in haematologic malignancies across Australia. This role is ideal for a medically trained professional seeking to expand into clinical development and medical leadership within industry.Responsibilitie...

Quality Assurance Consultant
ThuringiaNegotiable

Quality Assurance Consultant - Medical Device Manufacturing (Thuringia 🇩🇪) Join a leading innovator in medical technology on a critical quality project in Thuringia! We're seeking an experienced Quality Assurance Consultant to drive compliance, product integrity, and adherence to international standards across the device lifecycle.📍 Location: Th...

Senior Mechanical Engineer
LimerickNegotiable

Senior Mechanical Engineer - 12-Month Freelance ContractLocation: Limerick- On-site (minimum 3 days per week)Start Date: ImmediateWe are seeking an experienced Mechanical Design Engineer to lead the design and development of a new product. This is a hands-on role that combines conceptual design with practical implementation, requiring a strong foun...

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Selby Jennings Start Your Career In Recruitment
Director of Downstream Process Development CMC
BostonUS$200000 - US$235000 per year

Director, Downstream Process DevelopmentLocation: Greater Boston AreaPosition Summary:Currently partnered with a leading clinical-stage biotech that is developing several first-in-class traditional biologics across multiple stage development. They are looking to bring on an experienced Director of Downstream Process Development to spearhead their l...

Senior Clinical Data Manager
Palo AltoUS$180000 - US$190000 per year

Are you ready to make an impact in the fight against blindness? Join a cutting-edge biopharmaceutical company dedicated to developing transformative therapies for retinal diseases. We are seeking an experienced senior CDM to ensure the integrity, compliance, and readiness of clinical trial data that drives regulatory success and improves patient ou...

SR Manager/Associate Director Med Writing
BostonUS$150000 - US$185000 per year + bonus & stock options available

Regulatory Writing & Document DevelopmentLead the creation of key regulatory documents, including clinical overviews, summaries, and study-specific content for major submissions.Draft and update clinical study reports, investigator brochures, and standard operating procedures.Contribute to protocols, amendments, statistical analysis outputs, briefi...