4 beste Stellen als clinical research in basel, bs – aktuell auf Personalsuche

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Senior Manager - Post-Market Clinical Follow-up

Straumann Group -
Basel, BS

Jetzt bewerben

Details zur Stelle

100% | Pensum: 90-100%
vor 6 Tagen

Qualifikationen

Klinische Erfahrung
Kommunikationsfähigkeit

Vollständige Stellenbeschreibung

We are seeking an experienced and highly motivated professional with strong expertise in Post-Market Clinical Follow-up (PMCF) or Clinical Evaluation within the medical device industry. This position is part of Straumann’s Real-World Evidence (RWE) Team and is based at Straumann Group Headquarters in Basel, Switzerland. The role requires a collaborative and solution-oriented professional who is comfortable working across functions and managing diverse activities in an international environment. Reporting directly to the Team Lead RWE, the successful candidate will play a key role in driving PMCF strategy and execution in alignment with regulatory requirements and broader business objectives.

Key Responsibilities:

Oversee and continuously enhance PMCF processes and methodologies and contribute to Notified Body audits and technical file review activities
Evaluate and synthesize clinical data from multiple sources, including scientific literature, registries, surveys, clinical investigations, and scientific meetings
Establish, maintain, and track PMCF Plans / Reports, including oversight of associated activities, timelines, and deliverables
Support the integration of PMCF outputs into Clinical Evaluation and Post Market Surveillance documentation
Establish and, where applicable, implement methods for collecting post-market clinical data outside of clinical investigations (e.g. registry analyses, surveys, real-world evidence initiatives) in collaboration with internal and external stakeholders

Required Qualifications:

Advanced degree in a relevant field such as Life Sciences, Biomedical Engineering, Dentistry, or related disciplines
Minimum 5 years of relevant professional experience in PMCF, Clinical Evaluation, Clinical Research, or related fields within the medical device industry
Strong understanding of EU MDR requirements related to PMCF, Clinical Evaluation, and Post-Market Surveillance
Strong affinity for clinical and scientific data, including experience translating clinical evidence into regulatory documentation
Experience with post-market evidence generation approaches such as clinical investigations, registries, and surveys is strongly preferred
Excellent analytical, organizational, and communication skills with a structured, proactive, and result-oriented working style
Ability to manage multiple priorities effectively in a dynamic cross-functional and international environment

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or disability.

Employment Type: Full Time

Alternative Locations: Switzerland : Basel

Travel Percentage: 0 - 10%

Requisition ID: 21128

Jetzt bewerben

Erweiterte Suche

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