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Medical Writing Manager

Employer
Warman O’Brien
Location
Europe
Salary
Competitive Annual Salary plus Bonus and Benefits
Start date
28 Sep 2022
Closing date
28 Oct 2022

View more

Discipline
Medical Communications, Medical Writing
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details

An experienced Medical Writing Manager is required to join a top 5 global CRO on a permanent basis. This is a fully remote role; applicants can be based in most European countries. 

Within this role, you will act as Lead Medical Writer on any type of writing project, including projects with multiple deliverables/components. You will prepare assigned documents in accordance with Standard Operating Procedures and customer requirements as well as to the agreed timelines.

Additionally, you will perform senior review of all types of medical writing deliverables whilst also providing feedback and guidance to more junior staff.

Additional responsibilities will include:

  • Negotiates timelines and discusses/resolves customer comments.
  • Keeps abreast of current medical and/or technical writing/regulatory knowledge, including Good Clinical Practice (GCP), along with developments and advances in drug development/medical and/or technical writing.
  • Take a leading role in preparing assigned documents, including, but not limited to, confirming the scope of the task, confirming templates and specifications, negotiating and adhering to timelines, organizing document reviews, communicating directly with the customer.
  • Plan and organize workload for assigned projects and tasks: identify project needs, track timelines and implement customer requests.
  • Chair meetings. Able to act as point of contact for escalations and resolve conflict.
  • Participate in bid defense meetings and discussions.
  • Complete project finance activities, including monitoring and forecasting budgeted hours.
  • Independently propose, review and approve budgets and assumptions for a range of project types within remit.
  • May act as Project Manager for a small series of Medical Writing projects, that may involve elements of other functions.

What you can bring to the role:

  • 5+ years of CSR and protocol writing experience within pharma/clinical research
  • Minimum Bachelors Degree in life sciences related discipline or related field
  • In-depth knowledge of the structural and content requirements of clinical study reports, protocols, and similar documents and ability to identify deficiencies, errors, and inconsistencies in documents.
  • Good understanding of common statistical methods used in clinical trials and/or interpretation of their results.
  • Extensive experience in preparing CSRs and protocols independently to a consistently high standard, regardless of complexity or challenges.
  • Experienced in preparing CTDs and/or tackling new/unusual document types/customer requirements.

What you get in return:

  • The opportunity to work with a world leading CRO
  • A fully remote role
  • Competitive salary plus bonus and benefits

Company

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Warman O’Brien is a global specialist Life Sciences Recruitment Partner across the UK, Europe, USA and APAC. We recruit top talent across a number of functional areas including:

  • Biometrics
  • Data Sciences
  • Quality Assurance
  • Regulatory Affairs
  • Clinical Research
  • Discovery Sciences
  • C-Suite
  • Medical Affairs

We cover contract and permanent vacancies, executive search, and SOW for companies across the pharmaceutical industry.  

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Find out more on our website warmanobrien.com/

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Company info
Website
Telephone
+44 (0) 2033255075
Location
Floor 5
Regal House
70 LONDON ROAD
Twickenham
TW1 3QS
United Kingdom

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