Responsibilities
As a Medical Writer, you will be responsible for writing, editing, and finalizing project documents.
This involves:
- Writing clinical study reports (CSR)
- Writing clinical study protocols
- Writing protocol amendments
- Preparation of journal manuscripts
- Creation of posters and presentations
Requirements
Education:
- Master's degree or PhD in Science, preferably in a biological- or medical-related field
Experience:
- 3 years of experience with scientific writing
- Experience with the conduct of clinical trials is a plus
Skills:
- Excellent verbal and written skills in English - knowledge of Dutch or French is a plus
- Excellent knowledge of MS Office
- Excellent organizational and time management skills
- Excellent communication and problem-solving skills
Key competencies
- Integrity
- Focus with an eye for detail
- Achievement orientation and high energy
- Excellent communication & collaboration skills
- Respect for deadlines
- Can do attitude and the flexibility to engage in a variety of tasks
- Entrepreneurial mindset with a customer obsession
- Growth mindset to continuously learn and stay on top of latest developments
- The ability to work autonomously, as well as collaboratively in a team, in an atmosphere where giving constructive feedback is a must
We offer you
- A competitive package with extra-legal benefits (company car, mobile phone, meal vouchers, and insurances package)
- A young and dynamic work environment
- A strong commitment to your professional growth and continuous development
- A career path that is based on meritocracy with real growth possibilities
- An easy to reach office & possibilities to work from home. We promote hybrid working arrangements