(Senior) Clinical Research Specialist
Vor 7 Tagen
We are one of the world’s leading companies in the field of orthopedics, arthroscopy, sports medicine, and orthobiologics. True to our mission statement _Helping Surgeons Treat Their Patients Better_, we have been committed to developing innovative products and surgical procedures for over 35 years. Arthrex was founded in 1981 in Munich, Germany. Today our headquarters are based in Naples (Florida, USA) with a large network of subsidiaries in 21 countries. Our corporate culture is shaped by transnational cooperation as well as the exchange between colleagues of different nationalities. The opening up of new business fields and expansion of our product range help to secure continuous growth and enable us to take a leading role in the development of high-quality products both today and in the future. A major factor in this success is the commitment of our employees, in return for which we offer a motivating work environment where staff are valued and treated with respect.
To support our department Orthopedic Research in Munich or Lyon (France), we are currently offering a position as
**(Senior) Clinical Research Specialist (f/m/d)**
**Your Tasks**
- You coordinate medical device clinical studies in the EMEA region. Your focus are French-speaking countries
- You act as the link to sites and global project members from other departments
- You ensure compliance with national requirements in France (e.g. CNOM / ARS submissions)
- You grow and maintain the collaboration network in French-speaking countries
- You carry out literature and data research on current topics in the fields of orthopedics and sports medicine
- You work closely with the regulatory department to address clinical questions
- You develop and enhance operating procedures in accordance with relevant clinical research standards
- You operate in your function at the Munich and Lyon offices (the primary workplace can be either of these two locations)
**Your Profile**
- You hold a degree in Natural Sciences/a comparable field or have a equivalent qualification
- You equally enjoy regulatory and scientific work
- You have prior experience in clinical project management or in a coordinating function in the medical device industry
- You are familiar with relevant international regulations, standards, and guidelines such as the MDR, ISO 14155 or the Declaration of Helsinki as well as local requirements such as the "Code de la Santé Publique"
- You find it easy to produce scientific texts
- You can interpret complex technical instructions and surgical procedures
- You appreciate working in an innovative, dynamic, and global team
- You have strong communication skills, work independently, and act responsibly
- You are flexible and enjoy traveling
- Very good written and verbal skills in French and English complete your profile
**What You Can Expect**:
- A role in an international working environment
- Personal and appreciative collaboration
- A future-proof position
- Flexible working hours and the option of mobile working in many areas
- Tailored initial training as well as comprehensive introductory training
- Company pension and free supplementary hospital insurance
- Free lunch from Monday to Thursday
- Reiner Kastizen- +49 89 90 90 05 5100**Contact**:
Arthrex GmbH | Erwin-Hielscher-Straße 9 | 81249 Munich, Germany
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