Design and initiate clinical studies, author protocols and reports, synthesize literature.
Build partnerships with universities and clinics across our global network.
Drive and assist in the preparation and review of essential documents such as study protocols.
Conduct on-site and remote monitoring visits to ensure proper documentation and protocol adherence.
Verify that clinical trial data is complete, accurate, and verifiable against source documents.
Collect, validate, organize, and manage clinical study data.
Provide training and ongoing support to site staff on protocol requirements, GCP, and regulatory guidelines.
Act as a liaison between TePe Oral Hygiene Products and study sites, providing regular updates on study progress.

Balans mellan arbete och fritid med flexibla arbetstider, hybridarbete och familjevänlig policy.
Generösa hälsoförmåner – inklusive friskvårdsbidrag, aktivitetsveckor, roliga utmaningar, gymrabatter och mycket mer.
Engagerande välkomstdagar och en dedikerad fadder.
Microlearning för att snabbt komma in i arbetet.
Hög medarbetarnöjdhet med 85 % deltagande i interna undersökningar.

TePe Oral Hygiene Products

Open Positions (1)