Medical Writer

As a Senior Medical Writer, you will be working in a fast growing and challenging environment within a large range of projects and various therapeutic areas!
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Job Description

Keyrus Life Science is looking for a Senior Medical Writer to join their team based in Waterloo. 

Your challenges will be : 

  • Synthesize literature review findings into reports in various therapeutic area; 
  • Write, edit and update clinical development related documents with the highest level of technical accuracy (clinical protocols, informed consent forms, study reports, investigator brochures, clinical trial results, annual reports, statistical analysis plans, briefing documents, paediatric investigational plans and other clinical documents);   
  • Lead the process of critical review of clinical documents and incorporate multiple reviews into successive drafts. Provide quality control (QC) support for clinical documents as needed; 
  • Ensure the quality of clinical documents by maintaining and promoting familiarity with International Council on Harmonization Good Clinical Practice (ICH-GCP) guidelines, and other standards; 
  • Liaise with authors and clients regarding scientific content ;   
  • Write, review and edit manuscripts, posters, abstracts, etc.; 
  • Attend internal and external team meetings; 
  • Respect quality commitments; 
  • Participate in the continual improvement of the Quality System; 
  • Identify, record and ensure corrections of non-conformities; 
  • Update the Medical Writing process and templates and ensure compliance with current regulatory guidelines and best practice; 
  • Assist with the development of business proposals related to Medical Writing functions (preparation of budget grids and financial and technical proposals for clients).

Besides your main tasks, you will also be responsible for the integration of newcomers and training of junior profiles which includes to: 

  •  Allow smooth integration of newcomers; 
  •  Supervise junior medical writers and ensure their training regarding applicable regulatory guidelines and medical writing practices. 

Profile

You have a degree or a Phd in Science with at least 3 years of experience as medical writer in a Contract Research Organisation (CRO), pharmaceutical, and/or biotechnology environment. You are Fluent in English (spoken and written) and have a good knowledge of ICH-GCP guidelines. You have a good understanding of the significance of clinical, epidemiological and scientific data in general. You are detail-oriented with strong a analytical and organisational mindset.

What we offer

At Keyrus, thanks to the expertise of our people and external partners, each employee is welcomed with a varied integration program. You will join a dynamic and international environment with enthusiastic and professional colleagues.

We invest considerable time and resources in training our staff (technical and non-technical courses) to continuously support you in your personal and professional growth. On top of this, you will receive a complete salary package including attractive extra-legal benefits (company car, petrol card, meal vouchers, group insurance, hospitalization…) based on your background and experience.

Who we are

Keyrus Life Science is an international Consulting, Contract Research Organisation and Functional Services provider with a reputation for transparency and integrity, highly focused on being able to deliver with excellence. Our ‘human’ approach to service provision is what differentiates us from our competitors. Combined with our high caliber staff, this approach has allowed us to become a key player in clinical research.

At Keyrus Life Science we’re proud of our commitment to delivering services of the highest quality, not only skillfully, efficiently and reliably, but also with sincerity and genuine care for our clients’ projects, priorities and reputation. Thus we maintain and advance our vision and our standards, all the while ensuring that we serve your interests better

From early- to late-stage drug development, our range of services includes: Project Management, Clinical Operations, Pharmacovigilance, Quality Assurance (GxP), Regulatory Affairs Strategy & Support, Data Management, Medical Review & Coding, Biostatistics, Medical Writing & Medical Information, Real World evidence services.

We usually respond within a week

Or, know someone who would be a perfect fit? Let them know!

Waterloo

Drève Richelle 161
1410 Waterloo Directions

Our offices are the place where you are always welcome when you are not working on client's site or from home. Every single person that joins us is met in a personal and unique way.

What is really common to all of us, is the envy to contribute to the improvement of people’s health. Every employee being part of Keyrus Life Science is therefore fully committed to making the world a better place to live.   

With us, you will be part of our family and feel our human approach culture as of Day 1! 

Already working at Keyrus Life Science Belgium?

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