
1001 - 5000 employees
Founded 2018
💊 Pharmaceuticals
🔬 Science
🤝 B2B
Pharmaceuticals • Science • B2B
CenExel is a U. S. -based clinical research site network operating multiple Centers of Excellence nationwide that run and support clinical trials to advance new therapies. The company partners with life science and pharmaceutical sponsors to manage participant recruitment, trial operations, and data collection, emphasizing patient experience, quality, and scientific rigor. CenExel also offers a mobile app to connect patients with trials and participates in multisite research collaborations to accelerate drug development.
🕒 April 21
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1001 - 5000 employees
Founded 2018
💊 Pharmaceuticals
🔬 Science
🤝 B2B
Pharmaceuticals • Science • B2B
CenExel is a U. S. -based clinical research site network operating multiple Centers of Excellence nationwide that run and support clinical trials to advance new therapies. The company partners with life science and pharmaceutical sponsors to manage participant recruitment, trial operations, and data collection, emphasizing patient experience, quality, and scientific rigor. CenExel also offers a mobile app to connect patients with trials and participates in multisite research collaborations to accelerate drug development.
• Oversees the planning, execution, and close-out of clinical research studies • Ensures operational excellence, regulatory compliance, and timely delivery of study milestones • Leads cross-functional teams through all phases of clinical trial execution • Develops and manages project timelines and deliverables • Monitors progress against milestones and proactively address risks or delays • Tracks enrollment metrics, protocol deviations, and site performance • Serves as primary contact for sponsors and external vendors • Coordinates with sponsors, CROs, and internal teams to ensure alignment • Supports audit readiness and maintains complete, compliant documentation
• Bachelor’s degree in life sciences or related field • 4+ years of clinical research experience (Project Management experience preferred) • ACRP certification a plus • Strong knowledge of FDA regulations and ICH GCP • Proficiency in SharePoint, Excel, and project management tools • Experience with multi-site trials and sponsor/CRO collaboration, preferred • Familiarity with MedDRA coding and pharmacovigilance workflows
• Health Insurance • Dental • Vision • LTD • STD • Life Ins • 401k
Apply Now🕒 April 21
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