An excellent opportunity has arisen to join a leading pharmaceutical company as a Senior Medical Writer. The Senior Medical Writer develops study protocols and amendments, Informed Consent Forms (ICFs), Clinical Study Reports (CSRs), Investigator's Brochures (IBs) and other regulatory document...

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...

The Senior Manager, Regulatory Writing will report to the Director of Regulatory Writing. The regulatory writer will be responsible for writing and/or editing clinical documents for INDs, BLAs, MAAs, and associated regulatory submissions. Roles and Responsibilities (including, but not limited...

An excellent opportunity has arisen to join a leading pharmaceutical company as a Senior Medical Writer. The Senior Medical Writer develops study protocols and amendments, Informed Consent Forms (ICFs), Clinical Study Reports (CSRs), Investigator's Brochures (IBs) and other regulatory document...

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 ...

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...