Report Drafting Associate

☞ Labcorp

View: 107

Update day: 01-06-2024

Location: Harrogate Yorkshire and the Humber

Category: Pharmaceutical / Chemical / Biotech Printing / Publishing

Industry: Healthcare

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Job content

Job Overview:

Are you organised and have a keen eye for detail?


Do you have an interest in science but want to be office based?


Labcorp Drug Development is a global, world-leading Life Sciences Contract Research Organisation that provides dedicated and fully comprehensive laboratory testing and drug development services to the pharmaceutical industry. We strive to make a difference to people’s everyday lives by bringing essential medicines to the market.


We are currently seeking a Report Drafting Associateto join our Genetic Toxicology department in Harrogate.


Duties include:


  • Using information from the protocol and study files, prepare study reports for the Study Director containing factual information and study data.
  • Liaising with the Study Director to discuss details of the study and any special requirements for the report.
  • Preparing, formatting and checking reports to the scheduled deadlines according to Covance or client-specific requirements.
  • Preparing and quality checking tabulated summaries.
  • Assisting Study Director in addressing quality assurance inspection items on GLP-regulated studies, as required.


What Labcorp Drug Development can offer you:


  • Competitive salaries and a comprehensive benefits package including health cover and contributory pension.
  • Unrivalled opportunities to develop a successful career in the scientific industry.
  • Unsurpassed career development opportunities. With the support of exceptional people from across the globe and an energised purpose, you will be empowered to own your career journey with mentoring, training and personalised development planning
  • Paid overtime.

Education/Qualifications:

  • BSc degree or equivalent experience

Experience:

  • Basic knowledge of office software (e.g., Microsoft® Office, especially Word and Excel; Adobe® Acrobat®)
  • Attention to detail, time management skills, and organizational skills
  • Experience in technical writing, document production/publishing, and/or science desirable
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Deadline: 16-07-2024

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