Clinical Affairs Specialist (m/f/d)

Position: Clinical Affairs Specialist (m/f/d)

Industry: Life Sciences

Start Date: 01.10.2026

Duration: 6 months

Workload: 60%

Location: Switzerland, 2 days on site, 1 day Homeoffice

Responsibilities:

• Support Clinical Evaluation activities throughout the product lifecycle
• Review and update Clinical Evaluation Reports (CERs) and Clinical Evaluation Plans (CEPs)
• Support Post-Market Clinical Follow-up (PMCF) activities, including PMCF Plans, Evaluation Reports and PMCF strategy
• Assist with literature reviews and scientific evidence assessments
• Support clinical claims substantiation in collaboration with the Marketing team
• Contribute to risk management activities from a Clinical Affairs perspective
• Collaborate closely with Regulatory Affairs, Quality, R&D, Marketing and other cross-functional stakeholders
• Support product lifecycle management and upcoming product launch activities
• Provide day-to-day Clinical Affairs support across multiple ongoing projects

Qualification:

• Bachelor's or Master's degree in Life Science, Biomedical Engineering or related scientific dicipline
• Minimum 2 years of experience in clinical Affairs in the Medical Device indistry
• hands on experience
• Strong scientific writing and analytical skills
• Experience with literature databases such as PubMed, Embase and Chochrane is advantageous
• Fluent in English (writing and speaking)
• Ability to work in a cross-funcional team