Clinical Study Protocols jobs in Wilmington

Zenith LifeScience

The specialist study management assists in the coordination and administration of the study activities from the start up to execution and close out, and within the Local Study Team (LST) to ensure quality and consistency of interventional study deliverables to time, cost and quality objectives. Job

Zenith LifeScience

The specialist study management assists in the coordination and administration of the study activities from the start up to execution and close out, and within the Local Study Team (LST) to ensure quality and consistency of interventional study deliverables to time, cost and quality objectives. Job

ICON Strategic Solutions

ICON Strategic Solutions is currently hiring for a Clinical Study Administrator (CTA level role) for one of our larger sponsor partnerships. This is an office based opportunity out of Wilmington, DE What You Will Be Doing: Collects, assists in preparation, reviews and tracks documents for the applic

The specialist study management assists in the coordination and administration of the study activities from the start up to execution and close out, and within the Local Study Team (LST) to ensure quality and consistency of interventional study deliverables to time, cost and quality objectives. Job

A clinical research organization in Wilmington, DE is seeking a Study Start‑Up Manager to lead clinical study start‑up activities. The role requires extensive experience in regulatory processes, site management, and ensuring compliance with local and international guidelines, specifically ICH-GCP. T

A global clinical research organization is seeking a Clinical Trial Associate in Wilmington, Delaware. This role involves managing vendor spreadsheets, participating in study team meetings, and supporting vendor management activities. Candidates should possess a Bachelor's degree or equivalent exper

A leading biopharmaceutical company is seeking a Local Study Associate Director in Wilmington, DE, to lead teams in the execution of clinical studies. Responsibilities include managing study commitments, ensuring compliance with regulatory guidelines, and overseeing site selection and monitoring. Th

The specialist study management assists in the coordination and administration of the study activities from the start up to execution and close out, and within the Local Study Team (LST) to ensure quality and consistency of interventional study deliverables to time, cost and quality objectives. Job

General Information Name Clinical Study Administrator Employment Type Temporary Position level Full-time Virtual/Remote? No Labor Category Scientific Date 13-Mar-2026 City Wilmington State Delaware Country United States Ref # 9247852100 Description & Requirements Description Think the best job oppor

A leading life sciences company is seeking a study management specialist in Wilmington, Delaware. This mid-senior level role involves coordinating clinical studies, managing documents, and ensuring compliance with regulatory standards. The ideal candidate will have administrative experience in the m

ICON Strategic Solutions

ICON Strategic Solutions is currently hiring for a Clinical Study Administrator (CTA level role) for one of our larger sponsor partnerships. This is an office based opportunity out of Wilmington, DE What You Will Be Doing: Collects, assists in preparation, reviews and tracks documents for the applic

The specialist study management assists in the coordination and administration of the study activities from the start up to execution and close out, and within the Local Study Team (LST) to ensure quality and consistency of interventional study deliverables to time, cost and quality objectives. Job

Syneos Health/ inVentiv Health Commercial LLC

Clinical Project Manager II - Biomarker Study Management (Sponsor-Dedicated | Remote) Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization cont

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. What You Will Be Doing Vendor (e.g., CRO

ICON Strategic Solutions

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. *What You Will Be Doing** Organizes and

Clinical Trial Associate - US (Study Start-Up Support) ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinica

Clinical Study Administrator The Clinical Study Administrator (CSA) assists in the coordination and administration of the study activities from the start up to execution and close out, and within the Local Study Team (LST) to ensure quality and consistency of interventional study deliverables to tim