Clinical Safety Writer - Remote

Location
United Kingdom
Salary
Comprehensive Package
Posted
29 Jul 2021
Closes
28 Aug 2021
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

My client a mid-sized global CRO are looking for a Clinical Safety Writer to join their diverse, collaborative and inclusive Medical Writing team. The Clinical Safety Writer will carry out the creation of documents in accordance with client specifications, whilst maintaining written, Scientific and Ethical standards. If you are an experienced Medical Writer with extensive experience  within a Clinical Safety Environment please read below…

Responsibilities;

 

  • Preparation of study documents such as protocols, informed consent documents, CSRs, patient narratives investigator drug brochures, summary documents, and other documents in accordance with regulatory requirements Including QC/review of documentation as required
  • Coordination of internal and client document review cycles
  • Attend project-related meetings, as needed.
  • Serve as publishing point-of-contact in conjunction with the document coordinator to publish CSRs or other documents, as required
  • Create and manage project-specific timelines, adaptation of timing and milestones based on client requirements
  • Identify and communicate risks associated with document delivery and propose mitigation plan

Requirements;

  • Life science or related degree, Graduate degree preferred
  • Minimum of 3 years of clinical pharmaceutical industry
  • Excellent written and spoken English, able to accurately interpret data and express findings in a clear and concise written manner
  • Excellent project/time management and organisational skills
  • Comprehensive Microsoft Office specifically Word, PowerPoint and Excel 
  • Attention to detail—style, consistency, grammar, syntax, scientific accuracy
  • Thorough knowledge of applicable regulatory requirements and guidelines in particular ICH E3, E6, and E9

Benefits;

  • Competitive basic salary
  • Enhanced bonus scheme
  • Enhanced Pension and Healthcare schemes
  • Clear development pathway and training

Following your application Daniel Hockaday, a specialist Pharmaceutical Recruiter with 4 years’ experience as a specialist recruitment Consultant will discuss the opportunity with you in detail. He will be more than happy to answer any questions relating to the industry and the potential for your career growth. The conversation can also progress further to discussing other opportunities, which are also available right now or will be imminently becoming available.

This position will be very competitive, and it is likely that it will close prematurely. We recommend applying as soon as possible to avoid disappointment. Please click ‘apply’ or contact with Daniel Hockaday for any further information.

Daniel .C. Hockaday

Pharmacovigilance, Drug Safety & Medical Safety Surveillance Lead

Email: Dhockaday (at) barringtonjames.com

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