Senior Medical Writer - Belgium

Employer
i-Pharm Consulting
Location
Brussels, Belgium
Salary
Negotiable
Closing date
24 Sep 2020

View more

Discipline
Medical Communications, Medical Writing
Hours
Full Time
Contract Type
Contract
You need to sign in or create an account to save a job.

Senior Medical Writer - Belgium

Home based role - need to be based in Belgium. Occasional travel to Brussels once or twice per month

12 month freelance contract

Job Description

Provides high-quality medical and scientific writing from planning and coordination of literature search through delivery of final drafts to internal and external clients.

Provides technical consultation and provides substantive advice on strategy, regulations and industry best practices.

Demonstrates subject matter and therapeutic area expertise.

Effectively manages medical writing projects to deliver quality products in agreed timelines.

Collaborates with internal and external clients, supporting and enabling effective and efficient communication that results in operational excellence.

Independently researches, writes, and edits clinical study reports, study
protocols and standard response documents.

Produces complex clinical or scientific documents, such as, IBs, and sections of INDs, NDAs, CTDs, and dossiers.

Provides senior review of documents and training/mentoring for other
writers.

Manages all aspects of planning, organizing, and executing projects without
supervision including: developing project timelines, standards, budgets,
forecasts, and contract modifications.

Liaises with other functional units as necessary (i.e., project management, clinical, QA, data management, biostatistics, regulatory).

Identifies and escalates out-of-scope project activities in a timely manner and proposes solutions.

May manage several long-term projects concurrently.

Represents Medical Writing in Project Launch Meetings, Review meetings, client
audits, bid defenses, and capabilities presentations.

Establishes and develops client relationships; independently initiates and leads
interactions with clients.

Assists with business development and development of budgets and proposals.

Education and Experience:

- Must have breadth of regulatory writing experience (including, but not limited to clinical protocols, informed consents (ICFs), clinical study reports (CSRs), investigator brochures (IBs), patient narratives, annual reports, and other key clinical and regulatory submission documents)

- Bachelor's degree in a scientific, medical or clinical discipline or related field required, PhD preferred

- Minimum of 5-7 years of pharmaceutical/biotechnology related medical writing experience required

Life Sciences recruitment is what we do.

We are an award-winning international life sciences recruitment company with offices in London, New York, Munich, Singapore and Sydney.  In a highly competitive market-place, we connect top talent with the very best opportunities.

 

Our clients include many of the most successful and innovative Pharmaceutical, Biotechnology, and Medical Devices companies, as well as a range of Contract Research & Manufacturing Organisations, Healthcare Agencies and Consultancies.

 

With offices across 3 continents, we have teams servicing the major global life science hubs. We combine local knowledge, with a global network of contacts that allows us to bring together talent and opportunity when it matters most.

Contact Us
  • 212 New King’s Road
  • London
  • SW6 4NZ
  • GB
  • +44 (0) 20 3189 2299
You need to sign in or create an account to save a job.

Get job alerts

Create a job alert and receive personalised job recommendations straight to your inbox.

Create alert