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Job Details

Senior Medical Writer (Regulatory)-135454

Company: PPD
Location: Europe, Middle East & Africa-UK-England-Cambridge,
Reference: 135454
Closing Date: 21 Sep 17
Type: Full Time
Salary (£): On Application
Benefits:

Job Summary:

As part of our on-going growth, we are currently recruiting for a Senior Medical Writer to join our rapidly expanding team of over 90 regulatory writers based in Europe, North American and Asia Pacific. ...

Requirements:

As part of our on-going growth, we are currently recruiting for a Senior Medical Writer to join our rapidly expanding team of over 90 regulatory writers based in Europe, North American and Asia Pacific.

 

The Phase II-IV Medical Writing group, which is part of the Biostatistics Department, includes Writers who prepare documents in support of clinical trials and who assist Regulatory Affairs professionals with marketing applications, INDs, paediatric investigational plans, clinical trial applications, and other types of regulatory documents. 


Our writers possess strong leadership and project management skills, are creative problem solvers and decision makers, are engaging mentors and enthusiastic members of the department with an eagerness to continually improve our offerings and deliver a market leading service to our clients. In return, the medical writing department offers a highly competitive compensation package together with excellent opportunities for personal development and progression within the field. All within a friendly, fast paced and exciting environment.


The Medical Writer collaborates with internal and sponsor team members to interpret, distill, and summarize complex data concepts. Other tasks include presentation of clinical messages in clinical study reports, summarisation of preclinical and clinical studies for preparation of investigator's brochures, and referencing current research and regulatory guidelines for preparation of protocols. Their work documenting clinical study trials covers a wide range of therapeutic indications.


Qualifications

  • Education to Bachelor’s/advanced degree level in a scientific discipline
  • Prior experience within regulatory medical writing
  • Excellent grammatical, editorial and proofreading skills
  • Effective organisational and planning skills
  • Motivation, initiative and adaptability
  • Ability to work effectively in a team

The successful candidate can look forward to job stability with a leading CRO that has experienced year-on-year growth. We offer a generous salary and benefits package as well as excellent learning and development opportunities. We understand that the best writers are not necessarily on our doorstep, so if you are looking for a home based role we can offer this option to the right candidate, providing everything you need to fulfil your potential from your home office. This position can be home or office based in UK, Spain or Switzerland.

  We look forward to receiving your application.


Apply for this job: Senior Medical Writer (Regulatory)-135454

Contact Information:

Address:  PPD Cambridge
Granta Park
Great Abington
Cambridge

CB21 6GQ
England
Tel:  +44 1223 374100
Website:  Visit Our Web Site

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