Eylem Sentürk's Location
Switzerland
Eylem Sentürk's Work
- Team Lead Regulatory Document and Renewal Office @ Bayer Pharmaceuticals
- Senior Manager Development Quality, Compliance and Regulatory Affairs @ Novartis
- Founder and Managing Director @ Eds Regulatory Consulting GMBH
- Regulatory Affairs Manager @ CSL Vifor
- Senior Manager Regulatory Operations Europe, Cta Group Leader @ Celgene
- Manager Regulatory Operations Europe @ Celgene
- Dra Junior Clinical Trial Manager @ 爱可泰隆医药技术(上海)有限公司
- Dra International Manager @ 爱可泰隆医药技术(上海)有限公司
Eylem Sentürk's Education
- University of Liverpool
Master of Science (Applied Psychology)
2013 - 2016 - Forum Institut2013 - 2013
- RAPS Online University2013 - 2013
- London School of Hygiene and Tropical Medicine, U. of London
(Management, Statistics)
2011 - 2011
Eylem Sentürk's Skills
- Clinical Trials
- Pharmaceutical Industry
- Regulatory Affairs
- Regulatory Submissions
- Oncology
- GCP
- Pharmacovigilance
- ICH-GCP
- Sop
- Clinical Operations
Eylem Sentürk's Summary
Eylem Sentürk, based in Switzerland, is currently a Team Lead Regulatory Document and Renewal Office at Bayer Pharmaceuticals, bringing experience from previous roles at Novartis, Eds Regulatory Consulting GMBH, Vifor Pharma and Celgene. Eylem Sentürk holds a 2013 - 2016 Master of Science in Applied Psychology @ University of Liverpool. With a robust skill set that includes Clinical Trials, Pharmaceutical Industry, Regulatory Affairs, Regulatory Submissions, Oncology and more, Eylem Sentürk contributes valuable insights to the industry. Eylem Sentürk has 4 emails on RocketReach.
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