- Principal Medical Writer
As part of our on-going growth, we are currently recruiting for a Principal Medical Writer to join our rapidly expanding team of over 60 regulatory writers based in Europe, America, India and China
- Senior / 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 both regulatory and clinical trial writing, predominantly in phase III across a wide range of therapy areas. Brilliant opportunity to join a fast-paced organisation with great prospects for career progression.
- Senior/Principal Medical Writers - London, Manchester,Oxford
As a Senior/Principal Writer, you will need to have the right blend of experience to not only produce high-quality communications, but be able to lead a team of more junior writers, interact and liaise directly with clients and industry gurus. Sound writing skills, supported by a Life Science degree at the very least, coupled with an ability to multi-task, project manage and deliver projects of the highest quality at all times.
- Associate Editorial Director - London - MedComms Agency
As an Associate Editorial Director, you will work closely with the Editorial Director to provide editorial, scientific and strategic expertise to leading international pharmaceutical clients and colleagues within the agency. You will lead discussions in client meetings / teleconferences and work in partnership with Client Services Directors to provide leadership of account teams to ensure client expectations are achieved.
- Editorial Team Leader - Medical Communications
Editorial Team Leader, Editorial Manager, ETL
London, United Kingdom
£45k - £65k (Negotiable and dependant on experience)
Competitive benefits with a few extras to sweeten the deal
Friendly informal working environment
In-house and external training
Opportunities to transfer your skills to other offices around the world.
- Senior Medical Writer, Home-Based
This is a home-based Senior Medical Writing role within this large MedComms company where you will be required to work within a team and report to a team lead who specialises in Scientific solutions. This is an exciting role where you will be responsible for both the development and delivery of large scientific projects for specific accounts. You will also have the opportunity to travel within Europe and the USA
- Senior Medical Editor - London
SENIOR MEDICAL EDITOR -MEDCOMMS- LONDON
A global medical communications agency powered by energy and scientific strength. They have grown to be a leader in their field. With a very talented team of people, and a very impressive client list - word on the street is they are a pretty high on the '#1 company to join' list.
- 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, 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
- Medical Writer, Regulatory, Cambridgeshire/Norfolk
SENIOR MEDICAL WRITER, REGULATORY, CAMBRIDGESHIRE/NORFOLK/EASTERN 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 d