Pharmiweb ChannelsAll | PharmaCo | Clinical Research | R&D/BioTech | Sales/Mktg | Healthcare | Recruitment | Pharmacy | Medical Comms

Pharmiweb.com RSS Feed Pharmiweb.com RSS Feeds

Job Details

(Contract) Senior Medical Writer - International CRO - Remotely based - 12 months

Company: Meet
Location: Remotely Based
Reference: GCMW0301
Closing Date: 28 Feb 18
Type: Contract
Salary (£): Competitive
Benefits:

Job Summary:

An International CRO are urgently seeking a freelance Medical Writer, with expertise in CSRs and CTD modules 2.5 and 2.7, to join their global medical writing team. This is a remote 12-month contract, starting ASAP. The company are ideally looking for a candidate based in the UK.

Requirements:

For over 30 years this international Clinical Research Organisation have assisted in developing approximately 90-5% of the 200 top-selling biopharmaceuticals products. Partnering with all the top 20 biopharmaceutical and biotechnology companies and with operations in over 70 locations this is an unmissable opportunity to join a market leading CRO.

You will be the primary writer for a variety of regulatory documents, primarily CSRs and CTD modules 2.5 and 2.7. This is a remotely based, full-time position. For some candidates part-time work maybe available (a minimum of 28 hrs/week).

 

Contract Senior Medical Writer - International CRO - Remotely based - 12 months

Get in touch with Georgina Collings at Meet to discuss this or similar roles further!

 

Key responsibilities:

  • Write clinical documents for submission to regulatory authorities including briefing documents, clinical development plans, previous human experience summaries, human pharmacology summaries, investigator brochures, study protocols, model informed consents, interim and final clinical study reports, common technical document (CTD) clinical overviews and summaries, safety update/aggregate reports, integrated summaries of safety and efficacy.
  • Act as the primary client contact; negotiating timelines and resolving or escalating any issues.
  • Coordinate the production of draft and final documents and distributed these to the project team and client.
  • Maintain timelines and workflow of writing assignments.
  • As a Senior Writer you will be involved in mentoring junior medical writers.

 

Key skills:

  • Educated to Bachelor’s/advanced degree level in a scientific discipline, a MSc or PhD is an advantage.
  • A minimum of 5 years’ experience within a Pharma, CRO or Biotech writing regulatory and clinical documentation.
  • Experience as the primary author of CSRs and CTD modules 2.5 and 2.7.
  • The ability to understanding and analysis clinical data.
  • Experience as a project lead, or medical writing manager is an advantage.

This role is suitable for: Freelance Medical Writer, Medical Writing Contractors, Regulatory Writers, Technical Writers, Contract Medical Writers, Medical Writing Freelancers, Senior Medical Writer, Principle Medical Writer

 

Contract Senior Medical Writer - International CRO - Remotely based - 12 months

Get in touch with Georgina Collings at Meet to discuss this or similar roles further!

 

Keywords:

Medical Writer, Regulatory Writer, Scientific Writer, Clinical, Regulatory, Clinical Study Reports, CSR, CTD, Clinical Summaries, Clinical Overview, Protocols, Briefing Documents, Regulatory Authorities, CRO, Pharmaceutical, Bio-pharmaceutical, Biotechnology, FDA, MHRA, Phase II-IV, Therapeutic Areas, Oncology, remote, home-based.

Apply for this job: (Contract) Senior Medical Writer - International CRO - Remotely based - 12 months

Contact Information:

Address:  meet
Irongate House, 30 Dukes Place, London
EC3A 7HX
England
Tel:  +44 203 178 7488
Website:  Visit Our Web Site

Advertising
Site Map | Privacy & Security | Cookies | Terms and Conditions

PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.