Straumann Group has been a leader in premium implants for the last 75 years, becoming one of the largest players in the entire Implantology market with four more brands acquired over the decades. The expansion into Orthodontics and digital dentistry has been a focus area for the company in recent years to establish itself as an oral care company in specialty dentistry. As the company prepares for its ambitious 5B Goal, making commercial business models in Specialty workflows is the chosen path to become the Experience company focused on the patient at the center of all innovation.
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 report to the Global Clinical Research Portfolio and Data Team, located at Headquarters in Basel, Switzerland. Your workplace will be 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 including 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 the medical device / dental field is an advantage.
* Minimum 2 years of professional experience in medical writing and systematic literature searching including 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 working with an international team of Clinical Evaluation Specialists.
* Excellent verbal and written communication skills in English.
* Good analytical skills and ability to interpret data.
* Good knowledge of MS Office applications.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or disability.
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