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Consultant in Medical Writing (candidate pool)
Client:
Keyrus Life Science
Location:
Belgium
Job Category:
Other
EU work permit required:
Yes
Job Reference:
c68f01b4c0fd
Job Views:
25
Posted:
23.01.2025
Expiry Date:
09.03.2025
Job Description:
Job Description
Keyrus Life Science is looking for Medical Writers to join our consulting team for client projects ranging from big pharma to small biotech based in Belgium.
This job description serves as an example of the role. Once we have a specific project and client, you will be informed and have the choice to be presented to our client.
Your potential challenges could include:
* Synthesize literature review findings into reports in various therapeutic areas;
* 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 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;
* 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 practices;
* Assist with the development of business proposals related to Medical Writing functions (preparation of budget grids and financial and technical proposals for clients).
Some other technical jobs in Medical Writing might also require:
* The writing of price and reimbursement files for authorities and working in tandem with a Value and Patient Access Manager. Most of the content for the file will be delivered, but occasionally additional literature searches may be needed.
Profile
* 1 year of experience in Medical Writing is a must have. Contractors with experience in oncology are an asset.
* Excellent writing skills to effectively and clearly communicate in French and English.
* Scientific degree (quick understanding of scientific information).
* Ability to communicate scientific or medical information clearly and concisely.
* Proficiency in Word, Excel, PowerPoint, EndNote (or similar system), email, and Internet.
* Familiarity with the principles of clinical research (e.g., use of clinicaltrials.gov).
* Ability to interpret and present clinical data and other complex information.
* Ready to take initiatives related to the improvement of templates.
* Organizational skills; accustomed to delivering on time.
* Ability to work on different projects in parallel.
What we offer
Joining our consulting team in Belgium means advancing your career. Thanks to our privileged partnership with well-established clients, we offer unique projects to develop your skills and accelerate your professional experience in the pharma industry.
As an expert on the client side, you can count on us to support you at each step of your project through regular touch points with our Key Account Manager. We will also carefully choose your next assignment to match your career goals, whether in Consulting or in one of our Functional Services Platforms.
We invest considerable time and resources in training our staff (technical and non-technical courses) to continuously support your personal and professional growth. Additionally, you will receive a complete salary package including attractive extra-legal benefits (company car, fuel 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 known for transparency and integrity, focused on delivering excellence. Our ‘human’ approach to service provision differentiates us from our competitors. Combined with our high-caliber staff, this approach has established us as a key player in clinical research.
At Keyrus Life Science, we pride ourselves on 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. We maintain and advance our vision and standards, ensuring 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, and Real World Evidence services.
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