Principal Medical Writer – Regulatory Lead

Senior/Principal Medical Writer – Remote/Hybrid/In Office - UK Location An Indegene Company (Trilogy Writing & Consulting), Cambridge, United Kingdom. Must reside in the UK, Germany, Italy, Ireland, or Portugal. Job Overview We are seeking Senior or Principal Medical Writers to create high‑quality regulatory documents for the international pharmaceutical...

Senior/Principal Medical Writer – Remote/Hybrid/In Office - UK Trilogy Writing & Consulting, An Indegene Company, is currently looking to hire Senior/Principal Medical Writers (f/w/d) to support our growing company in producing high-quality regulatory documentation for the international pharmaceutical industry. At Trilogy, you will be part of a team that...

**Job Title: Principal Medical Writer ** A major pharmaceutical CRO that are centred on offering a comprehensive list of world-class services across the clinical development spectrum. With scientific discovery, to assessing safety, efficacy, and health care outcomes, to managing clinical triallogistics, to the development and manufacturing of the drug...

Senior/Principal Medical Writer – Remote/Hybrid/In Office - UK Trilogy Writing & Consulting, An Indegene Company, is currently looking to hire Senior/Principal Medical Writers (f/w/d) to support our growing company in producing high-quality regulatory documentation for the international pharmaceutical industry. At Trilogy, you will be part of a team that...

A leading life sciences company in Cambridgeshire is seeking a Regulatory Affairs Manager to lead global regulatory activities across a product portfolio. In this pivotal role, you'll manage regulatory submissions and ensure compliance with international regulations. The ideal candidate will have over 5 years of experience in IVD or medical device...

Regulatory Affairs Manager A leading medical device and IVD manufacturer based in Cambridgeshire is looking for a Regulatory Affairs Manager. This company develops and supplies innovative diagnostic solutions used worldwide. As a Regulatory Affairs Manager, you’ll play a key role in ensuring products meet global regulatory, safety, and quality standards...

Health and Safety Lead at Principal People Join to apply for the Health and Safety Lead role at Principal People This range is provided by Principal People. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range An exciting opportunity has arisen for a Health and Safety Lead to join a leading...

A leading medical device manufacturer in Cambridge is seeking a Regulatory Affairs Manager to ensure compliance with global regulatory standards. The successful candidate will lead regulatory strategy, oversee submission preparations, and manage post-market activities. With over 8 years of experience in IVD and medical device regulations, the ideal candidate...

Regulatory Affairs Manager Location: Cambridgeshire Employment Type: (Full-time: Mon-Fri) (Hybrid: 2 - 3 days on site) We are seeking an experienced Regulatory Affairs Manager to lead global regulatory activities across a product portfolio and ensure the products remain safe, effective, and compliant for worldwide markets. This is an exciting opportunity for...

Get AI-powered advice on this job and more exclusive features. Principal People provided pay range This range is provided by Principal People. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range Well established company looking for a new Head of Sustainability and CSR – could this be your...