- Senior Medical Writer ( Clinical Trials ) - International CRO, South East
Senior Medical Writer to work at a Global CRO in the South East in Clinical Trials
- Senior Medical Writer – Split Office / Home based. Clinical Trials
Senior Medical Writer to work at a Global CRO in the South East within the area of Clinical Trials. 5 years of hands-on Medical Writing experience is required to include having been a Lead Medical Writer at a CRO or Pharmaceutical company. Up to 3-4 days of working from home a week will be considered after a setting in period.
- Senior Medical Writer – Contract, 6 months, Pharma client – Strong Rate – Copenhagen
Medical writer, clinical writer, study reports, freelance – Multiple contract positions have become available to work on 6 month, rolling contracts for this US consultancy but on site with an international biopharma. The positions are based in Copenhagen and are looking for those confident in Clinical study reports, protocols, investigator brochures from a clinical perspective.
Strong rates on offer and happy to consider those with notice periods – apply now.
- 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?
- Contract Medical Writer – Global Pharma, 6 months, CSRs, Protocols - Denmark
Fantastic long term contracts are available for Medical Writers ( Regulatory Writers ) to join this exciting, fast moving and growing consultancy. The positions are 6 month contracts, looking to work on-site for a global biopharmaceutical business in Copenhagen, Denmark. The roles are centred around clinical documentation – Clinical Study Reports, protocols, investigator brochures and patient narratives.
- PW 6343 Medical Writer
This is a challenging opportunity for a highly skilled medical writer and strong communicator to utilise their scientific knowledge in an important role with one of the world's leading healthcare companies. You will have responsibility for preparing a broad range of clinical and safety regulatory documents and work with key stakeholders in safety science, biostatistics, clinical science and regulatory affairs amongst others.
- Senior Medical Writer
This role will involve duties to research, author and edit, clinical documents, including clinical study reports, clinical evaluation reports, protocols and safety update reports. The senior medical writer will also provide writing support for more complex clinical documentation within various departments. They will mentor and support junior writers in the team.
- MEDICAL WRITER - United Kingdom
An outstanding opportunity to join one of the world’s leading contract research organisations and be part of a dynamic and growing international company. Join PRA Health Sciences as a Medical Writer and help realize your career potential.
- Principal / Senior Medical Writer
For a confidential consultation call Meghann Price on 0044 (0) 207 255 6665 or email your CV to firstname.lastname@example.orgPermanent - Principal / Senior Medical Writer - CRO
- Senior Medical Writer - office based Mumbai
Due to our continuing success and expansion, we are currently looking for Senior Medical Writer to work with our team in India - Mumbai. Full time, permanent role, office based. We have the flexibility to take on either an experienced Senior Medical Writer or Medical Writer.