Seref Celik
Clinical Operation Coordinator - Monitoring Clinical Project Management Leadership @Iqvia Germany
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WORK HISTORY
Clinical Operation Coordinator - Monitoring Clinical Project Management Leadership @Iqvia Germany
Lead the planning and implementation of the site monitoring and oversight strategy for assigned clinical trials, authoring risk assessments and monitoring plans while ensuring compliance with ICH‑GCP and regulatory requirements. I provide expert guidance to trial teams and CRAs, maintain sponsor oversight of CROs, and drive issue management, risk mitigation, and trend analysis throughout the study lifecycle. I oversee monitoring activities, conduct oversight visits, contribute to trial documentation and amendments, support communication with internal and external stakeholders, and ensure inspection readiness and high‑quality trial delivery from startup through close‑out
EDUCATION
mibeg-Institut Medizin Köln
mibeg-Institut Medizin Köln, Klinischer Monitor (CRA)
TU Dortmund University
Master, Chemie
ABOUT SEREF CELIK
I am a dedicated Clinical Research Associate with over 10 years of experience in clinical trials, specializing in oncology. With a strong academic background in chemistry and polymer science, I transitioned into clinical research and have been working at IQVIA since 2015, currently holding the position of Senior CRA II.My expertise includes leading monitoring activities, mentoring CRA teams, and collaborating closely with project managers and study sites. I have extensive experience in international trials across various therapeutic areas including oncology, endocrinology, rheumatology, neurology, and reproductive medicine.I am GCP-certified, fluent in German, English, and Turkish, and have been recognized with the Spotlight Award for excellence in clinical operations. I am passionate about contributing to high-quality, patient-focused research and driving successful study outcomes through teamwork, precision, and compliance.
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