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Bioscript Group
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Associate Regulatory Writer



Business Type: Medical Communications Agency
Job Type: Medical Communication
Job Level: Experienced (non manager)
Position: Full Time
Location: United Kingdom
Reference: ARW
Job Details:

Opportunity for aspiring Associate Regulatory Writers

Team, Respect, Ownership, Quality, Continuous Improvement….

Are you passionate about science and able to communicate clearly and accurately? Do you have a degree in science or pharmacy, perhaps with a higher degree or postdoctoral research experience? Would you like to make a real difference to patients’ lives and the quality of global healthcare? Why not start a career in regulatory writing within a fast-moving, dynamic company?

We are recruiting Associate Regulatory Writers to join our growing, forward-thinking, friendly agency. With training and support to help you develop to Regulatory Writer and beyond, we can offer a stimulating and rewarding career.

 

Location:      Macclesfield, Cheshire (10-minute walk from Macclesfield train station).

Job type:      Permanent, full-time.

Company information

Bioscript Group provides global regulatory writing services and healthcare communications to a wide range of international pharmaceutical company clients across multiple therapy areas. Our agency covers the full range of medical communications, including publications, medical meetings and digital programmes. Also offering specialist health economic and regulatory writing services, we provide many opportunities for personal and professional development. Bioscript is independently owned and has grown steadily since its inception in 2005, adding new clients and talented new staff every year. We are proud that clients we worked with in the beginning continue to work with us today. 

The role

This is an ideal opportunity for someone with a strong scientific education to develop the necessary skills to become a Regulatory Writer. As an Associate Regulatory Writer at Bioscript you will receive the necessary training to be able to: 

  • Produce a range of regulatory documentation to meet client needs, according to appropriate guidance.
  • Effectively and efficiently manage projects.
  • Work confidently with colleagues and clients to ensure that reporting objectives are met.
  • Understand the regulatory environment in which the pharmaceutical industry works.
  • Develop project management skills to manage competing projects.

Requirements

  • A degree in life sciences or pharmacy is essential; a higher degree or postdoctoral research 
    is desirable.
  • You must have excellent written and spoken English skills.
  • You must have excellent communication skills.
  • Knowledge of clinical trials, the pharmaceutical industry and drug development is an advantage.

Applications and interviews

  • Closing date for applications is Sunday 4 April 2021, with start dates from summer 2021.
  • The selection process will involve a writing test and short presentation, and interviews are planned to be held at our offices in Macclesfield, Cheshire.

Bioscript is committed to promoting a diverse and inclusive community - a place where we can all be ourselves and succeed on merit.

 

Bioscript is committed to promoting a diverse and inclusive community - a place where we can all be ourselves and succeed on merit.

 

This is a UK based role, and all offers of employment are subject to candidates being able to provide suitable documentary evidence of their right to work in the UK. 



Bioscript Posted by:: Bioscript (View all our vacancies)
Unless otherwise stated, if applying for a job, you must ensure that you are already authorised to work in the country in which the job is based
Posted: 10/02/2021 | NPJ Ref: 265423 | NPJ Original URL
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