- Parexel (Sacramento, CA)
- The Senior Clinical Research Associate ( Sr . CRA ) is responsible for the site management, site monitoring and close-out of assigned ... Clinical Practices (GCP), and the Sponsor's standards. The Sr . CRA is accountable for site management...the set-up, running and close-out of sites in a clinical trial . ** Monitoring Responsibilities and… more
- Boehringer Ingelheim (St. Joseph, MO)
- …regard for our employees. The Clinical Research Associate ( CRA ) conducts in-house and external monitoring to verify that reported data collected in ... monitoring visits in compliance with Guidelines for all study/ trial sites. + Monitors the progress of in-house studies,...(2+) years' experience in Human Pharma or Animal Health Research areas. SR CRA : +… more
- Xeris Pharmaceuticals, Inc. (Chicago, IL)
- …discipline. * 6+ years' experience as a Clinical Research Associate . * Extensive knowledge of trial oversight activities, GCP/ICH and federal ... Sr CRA will be responsible for monitoring clinical studies at the site level...needs of the organization._ **Job Locations** _US-IL-Chicago_ **Title** _Senior Clinical Research Associate ( CRA… more
- ICON Clinical Research (Naperville, IL)
- …shape the future of clinical development. We are currently seeking a Senior Clinical Research Associate ( CRA ) to join our diverse and dynamic ... Senior Clinical Research Associate ICON...team. As a Senior CRA at ICON Plc, you will...the study lifecycle. **What You Will Be Doing:** + Monitoring clinical trial sites to… more
- BeOne Medicines (San Mateo, CA)
- …across clinical trial operations. Minimum 2 years of experience in clinical trial monitoring or direct study management + Minimum 2 years ... required. + Experience in clinical operations as clinical research associate , clinical...(eg, Clinical Operations, Clinical Compliance, Clinical Monitoring , Clinical Trial… more
- ICON Clinical Research (Blue Bell, PA)
- CRA II and Senior CRA -... Research Associate . + In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. + ... US ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster...you will be doing** + Conducting site qualification, initiation, monitoring , and close-out visits for clinical trials.… more
- IQVIA (Overland Park, KS)
- Job Overview: Join our dynamic team as a Clinical Research Associate ! You'll play a pivotal role in monitoring and managing clinical trial sites ... we'd love to hear from you! IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life… more
- J&J Family of Companies (Somerville, NJ)
- …monitoring , and close-out activities. The Senior SM will partner with the Clinical Trial Leader (CTL) to ensure overall site management while performing ... We are searching for the best talent for a ** Senior Site Manager ( CRA )** to support MedTech...Data Management, Clinical Evaluations, Clinical Research and Regulations, Clinical Trial … more
- IQVIA (Overland Park, KS)
- …basis. + Financial Management: If applicable, manage site financials according to the clinical trial agreement and retrieve invoices as required by local ... and experience may be considered. + Regulatory Knowledge: In-depth knowledge of clinical research regulatory requirements, including GCP and ICH guidelines. +… more
- BeOne Medicines (Emeryville, CA)
- …**Essential Functions of the job:** * Perform and coordinate assigned aspects of the clinical monitoring process in accordance with GCPs and SOPs to assess the ... collection is met per contractual guidelines * Works with Clinical Trial Oversight Managers (CTOMs) and ... Operations experience * Minimum of 3-4 years of ( CRA ) monitoring experience in the pharmaceutical or… more