Medical Writer
Straumann
Madrid, Spain
About the job:
We are looking for you as our new Medical Writer (m/f/x). In this role (100%, 40hrs/week) you will be involved in regulatory medical writing for the Clinical Evaluation Team. You will be reporting into the Global Clinical Research Portfolio and Data Team, located at Headquarters in Basel, Switzerland. Your workplace is at Straumann group’s Southern European Hub located in Madrid, Spain.
Key Responsibilities:
- Supporting the Clinical Evaluation Team at Headquarters in Basel with Medical Writing tasks;
- Performing and documenting systematic literature searches;
- Writing scientific documents incl. Clinical Evaluation Plans/Reports, State of the Art documents, Scientific Statements;
- Reviewing relevant input documents for consistency and alignment.
About Ideal Candidates:
- University degree (M.Sc. or higher) in a relevant discipline (life sciences, medical, biomedical engineering). Knowledge in medical device/dental field is an advantage;
- Minimum 2 years of professional experience in medical writing and systematic literature searching incl. data extraction. Knowledge of clinical evaluation under MDR is an advantage;
- Openness and willingness to acquire new skills with relevant literature management tools and applications;
- Good organizational skills, systematic and structured working style;
- Detail oriented, quality driven, efficient and flexible;
- Team player who is open to work with an international team of Clinical Evaluation Specialists;
- Excellent verbal and written communication skills in English;
- Good analytical skills and able to interpret data;
- Good knowledge of MS Office applications.
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