- Principal Medical Writer - MedComms - Manchester
As a Principal Medical Writer, you will take on full responsibility for your own work and consistently demonstrate breadth and quality of writing across a broad range of medical and commercially focused materials. You will take on line management responsibility and provide ongoing mentoring and support to other writers. In addition, you will provide strategic input into the business by contributing ideas to grow the business or improve efficiencies.
- Principal Medical Writer - Med Communications - Manchester
PRINCIPAL MEDICAL WRITER - MANCHESTER - MEDICAL COMMUNICATIONS AGENCY
My client is a global Medical Communications agency with over 100 employees worldwide. They are a super scientific agency that places the power of science above everything else. The company is rapidly growing, offers fantastic career prospects and gives you the support that can excel your career to new heights. Their success has led to continued expansion, both in the range of services they offer and their global presence.
- Medical Writer I to Principal Medical Writer – Global CRO – Office / Home Based
An international CRO is currently looking for a number of Medical Writers to join their team in the UK. You will be responsible for regulatory writing, predominantly in phase II and III across a wide range of therapy areas. Brilliant opportunity to join a fast-paced organisation with great prospects for career progression.
- Senior Medical Writer / Principal Medical Writer x 2
Two experienced Medical Writers required to lead, manage and mentor editorial teams, varying locations.
- Senior / Principal Medical Writer – Global CRO – Office / Home Based
An international CRO is currently looking for Senior / Principal Medical Writers to work office or home based throughout the UK. With over 60 Regulatory Writers globally this CRO have taken on high profile and very exciting project work with some of the leading Sponsors.
- Senior / Principal Medical Writer – Global Consultancy – Office Based (2 days from home)
A friendly growing consultancy is currently looking for a number of Medical Writers to join their team in the UK. You will be responsible for regulatory writing, across a wide range of phases and therapy areas.
- Senior/Principal Medical Writer – Medical Education Agency – Buckinghamshire/London - £40k-£60k (DOE)
Meet are proud to partner with this independent Medical Education agency, with state of the art offices based in Buckinghamshire & West London. They are specialists in their field and have developed and delivered successful Medical Education programmes globally for many of the world’s most impressive pharmaceutical brands and academic institutions.
- Senior Medical Writer - London - Medical Education
SENIOR MEDICAL WRITER - LONDON - MEDICAL COMMUNICATIONS (MED ED)
The role of the Senior Medical Writer is primarily to provide a high standard of written material with minimal supervision, across a broad spectrum of projects aimed at the pharmaceutical industry. These projects can and will range from highly scientific work involving extensive literature review and data assessment, to strongly market-orientated copy. As the SMW, you will be expected to be equally comfortable doing both.
- Senior Medical Writer - Glasgow - Medical Communications
SENIOR MEDICAL WRITER - MEDICAL COMMUNICATIONS - GLASGOW
A global healthcare communication and consultancy group that has not only been around for two decades, but has been successful and growing consistently throughout this time. They cover a wide range of areas which include world-class solutions in strategic consultancy, medical communication, pharmacy communication, real-world evidence, regulatory support, market access, and digital excellence.
- SENIOR MEDICAL WRITER, MEDICAL COMMUNICATIONS-Cambs/Norfolk
SENIOR MEDICAL WRITER, MEDICAL COMMUNICATIONS, CAMBS/NORFOLK/EAST UK
My client, a medical writing consultancy specialises in proactively planning, coordinating and writing clinical and medical communications documentation to meet aggressive timelines, with a readability that reduces the time for review and approval. They work with pharmaceutical companies and clinical research organisations globally, working to streamline their documentation processes and have been doing so for over a decade