Clinical Vacancies

Senior Medical Writer

Package: £45,000k

Location: London Bridge (UK, England, London)

Working Hours: 40 hours per week

We are the UK’s largest early Phase Contract Research Organisation (CRO) based within excellent facilities within London university hospital sites.

We have a great opportunity for a medical writer to join our team and expand their experience within the clinical research area.

You will be responsible for the production of clinical trial documents including Clinical Study Reports, and interim safety summaries. Working alongside our Research Physicians, Data Managers and Statisticians, you will research, write, edit and co-ordinate the production of these clinical trial documents.

Duties:

  • Effectively supervise & Manage a team of Medical Writers to deliver good quality documents within agreed timelines

  • Plan, prepare, write, edit, format, and finalize clinical and regulatory documents.

  • Documents will include, but are not limited to: clinical protocols, clinical study reports, Investigator brochures, Safety summary reports, regulatory submissions and annual updates as well as publications

  • Allocate resources and coordinate the internal review of documents.

  • Represent Medical Writing on project teams and, as such, advise teams on content and format requirements for various documents, as well as coordinate writing activities for document development (eg, timelines and review/revision responsibilities) with the project teams.

  • Ensure compliance, remain informed on regulations and developments in medical writing, as well as maintain knowledge of product areas, current trends, and current literature.

    Competencies:

  • Must have 3- 4 years’ experience of medical writing, ideally in a clinical trials environment

  • Should have a life science degree, PhD or MD with medical writing experience including first author of a minimum of two manuscripts.

  • Capable of understanding the underlying science and writing strategy related to assigned projects and writing more complex projects, (e.g. complex manuscripts and review articles)

  • demonstrates an ability to expertly use a range of resources (e.g. Microsoft office, scientific databases, referencing software, online submissions & tracking)

  • effectively train and manage associate medical writers, leading by example, is a team player, recognising where s/he can use his/her skills to support colleagues and direct reports

    In return we offer the opportunity to be a core part of our team of clinical professionals, a generous remuneration package, a contributory pension scheme, life assurance, private medical and dental cover and a generous holiday allowance.

    Please note that only shortlisted candidates will be contacted.

    NO Agencies please

 

 

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