Site Coordinator
Excelya(7 months ago)
About this role
An Associate in Clinical Operations at Excelya will join a dynamic CRO team contributing to clinical research projects and supporting innovation in clinical trial delivery. The role sits within a collaborative, fast-paced environment that emphasizes audacity, care, and energy and offers opportunities for professional growth across diverse study types. The position supports Excelya’s mission to be a leading mid-size CRO and to improve the patient journey through high-quality clinical operations.
Required Skills
- Clinical Monitoring
- Site Management
- CTMS
- TMF
- Centralized Monitoring
- Risk Monitoring
- Quality Review
- eCRF Design
- Team Supervision
- Regulatory Compliance
Qualifications
- Scientific Degree in Life Sciences, Pharmacy, or Nursing
- Master's Degree Preferred
About Excelya
excelya.comExcelya is a global contract research organization (CRO) that specializes in providing comprehensive full-service solutions, functional service provider (FSP) engagements, and resourcing solutions to the pharmaceutical and biotech industries. With a focus on excelling through care, Excelya supports its clients throughout the entire lifecycle of clinical development. Their expertise encompasses a range of services aimed at facilitating research and enhancing the efficiency of drug development processes.
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