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Medical Writer

Uppsala

Recruitment Life Science

Pharm Assist Sweden AB is a professional service company offering quality and regulatory solutions for medicinal products and medical devices. Founded in 1996 the company has assisted more than 200 pharmaceutical and medtech companies over the years. Pharm Assist’s highly qualified team of some twenty professional consultants has a strong scientific, business and regulatory experience and puts pride in providing tailor-made professional solutions in regulatory affairs and quality assurance for our clients. For more information, please visit, www.pharmassist.se

Due to increased client demands we are looking for yet another:

 

Medical Writer

 

On behalf of Pharm Assist Sweden AB, H&P Search & Interim is now looking for a Medical Writer. The position is located at the Pharm Assist office in central Uppsala, Sweden. Periodically you may also work at clients' offices, usually in the Uppsala or Stockholm area.

The role:

Working as a consultant in Medical Writing is mainly about writing larger reports for pharmaceuticals and medical devices, usually for regulatory purposes. The work is independent and involves own contacts with clients.

The work includes:

  • Plan and compile preclinical, clinical and pharmaceutical expert reports, eg Investigator's brochure, IMPD, Clinical Evaluation Reports etc

  • Write and maintain security monitoring documents, such as RMP, PSUR, DSUR

  • Compile and evaluate scientific literature and write scientific articles

Depending on past experience and skills, other tasks within Regulatory Affairs or Pharmacovigilance may also occur.

Qualifications:

  • M.Sc. or Ph.D. in medicine, pharmacy or natural sciences

  • At least 3 years of experience from working in the pharmaceutical industry, CRO companies, the pharmaceutical authority or similar

  • Speaks and writes fluent scientific English

Merit:

  • Previous work with medical/regulatory writing or the like

  • Previous work with development of pharmaceuticals or medical devices

  • Experience from pharmacovigilance and/or Regulatory Affairs

  • Certified in Medical Writing (Europe or North America)

  • Speaks and writes fluent Swedish

Profile:

  • Independent

  • Service-oriented (responsive to client requests and opinions)

  • Enjoy deep-diving into documentation and issues

  • Ability to closely follow guidelines and templates, but at the same time be able to work creatively & pragmatic within

  • Manages to work within set time frames and to report time carefully

Nest steps:

If this sounds interesting to you, contact one of us below for more information. Alternatively, you can apply directly by uploading your resume and by emailing us a line.

  

We look forward to your application!

Torbjörn Ströberg

+46 (0) 703 77 87 74

Leif Olsson

+46 (0) 706 99 47 80