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Bioscript Group
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Regulatory Writer - Macclesfield - Bioscript Regulatory

Business Type: Medical Communications Agency
Job Type: Medical Writing and Editorial, Regulatory Affairs
Job Level: Experienced (non manager)
Position: Full Time
Location: Cheshire
Reference: reg-wri-BR
Job Details:
Due to our successful growth, we are looking for Regulatory Writers to join our successful team. As a Regulatory Writer, you will work as part of a team preparing clinical regulatory documents across a diverse range of therapy areas for our pharmaceutical clients, utilising and broadening your existing experience in the industry. You will be familiar with documents such as clinical study reports, investigator brochures and the common technical document (CTD) modules, and have experience of the document production process. You will be able to evaluate scientific data objectively, in order to report results and scientific concepts in a concise and accurate manner.

Bioscript Regulatory is part of the Bioscript Group, an international, independent agency group, driving continuous improvement in healthcare standards and outcomes through inspirational scientific communications. We provide a full range of medical communication solutions, including specialist health economic and regulatory writing services, meeting and event support as well as a range of publication and digital services. Because we believe in enabling our employees to do what they do best, we recruit for excellence in specialised areas and provide many opportunities for personal and professional development. Based in East Cheshire, Bioscript has grown steadily since inception in 2005, adding new clients and talented new staff every year.

Why Bioscript?

• Science is at the core of everything we do
• We offer the opportunity to learn from regulatory/medical communications experts
• We take pride and ownership in the quality of our work
• We have a genuine focus on employee well-being
• We maintain a flexible working environment to help our team achieve a sensible work/life balance
• We offer a friendly, supportive and engaging environment in which individuals can thrive We are looking for candidates with drug development experience, relevant to the field of regulatory writing.

You will need a strong scientific background, including a minimum of a BSc (or equivalent) in an appropriate scientific discipline. You must have excellent written and spoken English skills, and a good working understanding of clinical development and ICH guidelines for regulatory documents. You should have a proactive approach, well developed project management skills, and confident and effective interpersonal skills. Flexibility for occasional travel within Europe is desirable.

Attracting and developing talent is key to our success and we will support you every step of the way to reach your full potential.

Posted: 31/10/2019 | NPJ Ref: 244439 | NPJ Original URL
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