An excellent opportunity has become available for a Principle Medical Writer to join an exciting Biopharma, based in Lausanne. Within this role you will be involved with the development of study-related documents, communication with health authorities, publications and presentations. You will ...

An excellent opportunity has become available for a Principle Medical Writer to join an exciting Biopharma, based in Lausanne. Within this role you will be involved with the development of study-related documents, communication with health authorities, publications and presentations. You will ...

The Medical Writer develops study protocols/amendments, informed consent forms (ICFs), clinical study reports (CSRs) and Investigator's Brochures (IBs) ensuring compliance with international requirements and manages the process of reviews, reconciliation of comments and document finalisation/ap...

An excellent opportunity has become available for a Principle Medical Writer to join an exciting Biopharma, based in Lausanne. Within this role you will be involved with the development of study-related documents, communication with health authorities, publications and presentations. You will ...

An excellent opportunity has become available for a Principle Medical Writer to join an exciting Biopharma, based in Lausanne. Within this role you will be involved with the development of study-related documents, communication with health authorities, publications and presentations. You will ...

Job Summary: An excellent opportunity has arisen for an experienced Regulatory Writer to join a growing CRO based in London. This role will offer the rare chance to either work remotely from home, or in the office. Role Overview: As a member of the Development Operations team, you will inte...

An excellent opportunity has arisen for a Senior Medical Writer to join an exciting and growing pharmaceutical company based in central London. Within this role you will be responsible for authoring clinical regulatory documents such as CSRs, IBs and INDs. Within this role you can either be o...

An excellent opportunity has become available for an experienced PV Writer to join my client based in Hertfordshire - 2 days home working is possible. Within this role you will be responsible for authoring Pharmacovigilance aggregate reports, including PBRERs, DSURs and RMPs. Evaluation of ...

Job Summary: An excellent opportunity has arisen for an experienced Regulatory Writer to join a growing CRO based in London. This role will offer the rare chance to either work remotely from home, or in the office. Role Overview: As a member of the Development Operations team, you will inte...

An excellent opportunity has arisen for a Senior Medical Writer to join an exciting and growing pharmaceutical company based in central London. Within this role you will be responsible for authoring clinical regulatory documents such as CSRs, IBs and INDs. Within this role you can either be o...

Job Summary: An excellent opportunity has arisen for an experienced Regulatory Writer to join a growing CRO based in London. This role will offer the rare chance to either work remotely from home, or in the office. Role Overview: As a member of the Development Operations team, you will inte...

Job Summary: An excellent opportunity has arisen for an experienced Regulatory Writer to join a growing CRO based in London. This role will offer the rare chance to either work remotely from home, or in the office. Role Overview: As a member of the Development Operations team, you will inte...

An excellent opportunity has arisen for a Senior Medical Writer to join an exciting and growing pharmaceutical company based in central London. Within this role you will be responsible for authoring clinical regulatory documents such as CSRs, IBs and INDs. Within this role you can either be o...

An excellent opportunity has become available for a Principle Medical Writer to join an exciting Biopharma, based in Lausanne. Within this role you will be involved with the development of study-related documents, communication with health authorities, publications and presentations. You will ...

An excellent opportunity has arisen for a Senior Medical Writer to join an exciting and growing pharmaceutical company based in central London. Within this role you will be responsible for authoring clinical regulatory documents such as CSRs, IBs and INDs. Within this role you can either be o...

An excellent opportunity has arisen for a Senior Medical Writer to join an exciting and growing pharmaceutical company based in central London. Within this role you will be responsible for authoring clinical regulatory documents such as CSRs, IBs and INDs. Within this role you can either be o...

Medical Affairs Professional wanted for our Geneva based client in the pharmaceutical sector. Your experience/skills: * Scientific degree in a biomedical field, optometrist, Pharm. D. or engineering * 1+ years' working experience as Medical Affairs Professional or similar position with prov...

An excellent opportunity has become available for a Principle Medical Writer to join an exciting Biopharma, based in Lausanne. Within this role you will be involved with the development of study-related documents, communication with health authorities, publications and presentations. You will ...

An excellent opportunity has become available for a Principle Medical Writer to join an exciting Biopharma, based in Lausanne. Within this role you will be involved with the development of study-related documents, communication with health authorities, publications and presentations. You will ...

One of our global CRO clients is currently growing in various therapeutic areas so, to support them in this, they are currently recruiting for a permanent Technical Writer vacancy for their regulatory affair and technical writing team. The successful candidate should be confident in regulator...

The candidate will be responsible for the production of clinical trial documents including Clinical Study Reports, and interim safety summaries. The candidate will be working alongside the company's Research Physicians, Data Managers and Statisticians, you will research, write, edit and co-or...

Medical Writer I am currently supporting a leading global agency that provides comprehensive and innovative medical communication solutions to the healthcare industry. They are currently recruiting for an experienced and enthusiastic Medical Writer with proven ability for generating and lea...

As well as a strong interest in medical writing, the ideal applicant will also have the ambition to develop their project management capabilities. Job responsibilities include but are not limited to the preparation of: * Clinical study protocols and protocol amendments * Investigational ...

ESSENTIAL FUNCTIONS: The responsibilities of this job include, but are not limited to, the following: * Write and/or coordinate with internal and external resources the clinical and related sections of INDs, NDAs, MAAs, CTAs, and similar documents. Resolve conflicting comments among reviewer...

Freelance Medical Writer - Diabetes/CV * To provide medical writing support to Corporate Department Medicine in the therapeutic area of diabetes * To support secondary analyses and publications from clinical trials and to maximize scientific & medical communication opportunities * To ser...