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Job Details

Principal Medical Writer (Regulatory)-141238

Company: PPD
Location: Europe, Middle East & Africa-UK-England-Cambridge,
Reference: 141238
Closing Date: 19 Sep 17
Type: Full Time
Salary (£): On Application
Benefits:

Job Summary:

As part of our on-going growth, we are currently recruiting for a Principal 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 Principal 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.

 

Duties and Responsibilities of the Principal Medical Writer will include:

  • Acting as key client contact

  • Preparing complex documents and providing review of others work

  • Advising on technical aspects of document preparation

  • Managing the business development and pricing projects for Medical Writing

  • Managing Project budgeting/forecasts

  • Assisting business development in securing new business

  • Reviewing revenue budgets and adjusting resources accordingly


Qualifications

To be considered for this position you will be able to demonstrate:

  • Education to advanced degree level in a scientific discipline

  • Strong and broad relevant regulatory writing experience

  • Prior experience in managing and directing complex medical writing projects

  • Prior experience with budgets and forecasts

  • Excellent grammatical, editorial and proofreading skills

  • The ability to mentor, motivate and integrate team members

  • The ability to manage and plan multiple complex projects

  • The ability to direct the work of others

The successful candidates 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.

 

We look forward to receiving your application.

Apply for this job: Principal Medical Writer (Regulatory)-141238

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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