Belgium Job Openings
Terumo Europe
Medical Writer
Leuven
November 30, 2024
Department Info
Job Summary
We are a leading medical device company that specializes in Therapeutic Interventional Oncology, a field that combines minimally invasive procedures with targeted therapies to treat cancer. We are looking for a Medical to join our European Medical and Clinical team and help us communicate our clinical evidence and scientific insights to various stakeholders.
In this role you will report to Christian Reul, Global Medical Development Program Lead Interventional Oncology and join up with a Medical Studies Coordinator in the European Medical and Clinical Division within Terumo Europe. Our European HQ is located in Leuven, Belgium. For this position we are open for remote work, if the candidate location is within reasonable distance from our headquarters. In addition you will also offer support to Christophe Van De Maele, our Medical Affairs Director Cardiovascular for EMEA, in creating scientific documentation and coordination of external resources.
Job Responsibilities
- Scientific intelligence and leading scientific literature review (excluding Radiation Oncology)
- Support publication & abstract submission for our clinical and medical program.
- Be involved in the development and dissemination of relevant clinical data
- Support the EMEA Medical Affairs Teams in answering unsolicited medical inquiries based on literature data.
- Responsible for implementing innovative and cost-efficient medical writing tools and systems (e.g. AI).
- Responsible for elaborating the scientific narrative and preparing the materials supporting the clinical claims used by product specialists in the field (e.g. master/speaker slide decks, one-pager summaries) on key strategic publications for the Holmium Platform portfolio in collaboration with cross-functional stakeholders and key opinion leaders. Support preparation of value dossier for Market Access purposes.
Profile Description
- An advanced degree in a Medical or Scientific domain
- 3 years experience working in a Medical or Scientific writing position
- Prior experience in Oncology or Cardiology is a strong asset
- Proven experience of collaborating with a geographically spread cross-functional team
- Fluent in English, one other European language is a plus
- Excellent written communication and presentation skills
- Excellent understanding of publication guidelines and practices (e.g. ICMJE, CONSORT, PRISMA)
- Excellent knowledge of online publication and clinical study databases (e.g. MEDLINE, Embase, Cochrane, Clinical Trials.gov, Eudra CT) and search tools and principles
- Knowledge of dedicated software and tools for literature search, storage and referencing (e.g. End Note, Mendeley) and eagerness to learn new tools and techniques
- Training in systematic literature search and analysis is a plus
- Analytical mindset with accuracy and attention to details
- Ability to derive key outcomes and messages from scientific reports and publications
- Willingness to adhere to rigorous internal quality standards (e.g. for clinical trial documents development, systematic literature search execution) and to contribute to process optimization and improvement
- Ability to work in a self-directed manner with a high degree of autonomy
Offer
As a Medical Writer you will be a vital member of our European Medical and Clinical team and enjoy a competitive compensation package, local benefits, and a company culture that fosters personal development. You will have the security of working for a financially stable organization that is dedicated to advancing the field of cancer treatment.
You will also have the opportunity to grow professionally and collaborate with external experts and key opinion leaders.
Join us and be part of a company that is committed to your success and our shared vision of quality and care. If this sounds like the perfect role for you, you can apply online with your CV and cover letter. We look forward to hearing from you and learning more about your qualifications and enthusiasm for this role.
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