- Regulatory Writer
My client is looking for a Medical Writer/Senior Medical Writer to join their successful team as a result of their services becoming in high demand. This is a fantastic opportunity to join a hugely successful company which will offer a highly competitive salary, great benefits and the chance to work a combination of home and office based.
- 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 Medical Writer - Home or Office Based UK
An exciting opportunity has arisen for a Senior Medical Writer to join a leading CRO that has experienced continuing growth. The role will be based in the UK and can be either home or office based.
- Senior Regulatory Medical Writer – Ireland
My client are a leading global pharmaceutical company who have a newly opened site located in Dublin, Ireland. To join a brand new team we are looking to appoint a Senior Regulatory Medical Writer.
- 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
- PW 6083 Regulatory Documentation Scientist / PV Med Writer
Here is a great opportunity to combine your scientific knowledge and writing skills in an important role with one of the world's leading healthcare companies.
You will be responsible for the project management and preparation of vital safety regulatory reports for innovative products and part of a global team driving the development of our client’s rich pipeline of new products to make a difference to the health and well-being of people across the world.
- Medical Writer
I am currently looking for a Medical Writer to draft, edit and reference scientific and medical peer review publications and study protocols for a global CRO. It's important that you attain and maintain an in-depth knowledge of therapeutic areas and products of relevance to client accounts. This is a full time, permanent position with excellent career development opportunities and great benefits.
- Experienced Medical Writers needed; Part HOME-BASED
I am recruiting for an experienced Medical Writer to draft, edit and reference scientific and medical peer review publications and study protocols for a global CRO. It's important that you attain and maintain an in-depth knowledge of therapeutic areas and products of relevance to client accounts. You will be an experienced Medical Writer with experience of Regulatory Writing.
- Medical Writer \ Lead Medical Writer
1 x Medical Writer, 1x Lead Medical Writer
Are you interested in working for one of the most respected and well known CROs in the pharma industry?
Are you an experienced medical writer who thrives on a busy and varied workload?
Would you like to communicate with colleagues and customers all over the world?
Do you want to fast track your career?
- Medical Writer – International Team – Berlin
As Medical Writer you will write documents for the Common Technical Dossier (CTD). Your main focus will be on clinical study protocols, investigator's brochures and clinical study reports. Additionally, you will write other regulatory documents including summaries and overviews. You will make sure that the documents are according to regulatory guidelines and will be submitted on time.