- Astellas Pharma (Boston, MA)
- …on Astellas, please visit our website at www.astellas.com . **Purpose and Scope:** A Clinical Site Monitor serves as the primary contact point between ... (GCP), and applicable regulations and guidelines from study start-up through to site closure. The Clinical Site Manager will manage the site /sponsor… more
- WuXi AppTec (Austin, TX)
- …be made and every disease can be treated." **Responsibilities** **Job Summary:** The Senior Clinical Research Associate is a critical position within the ... CRA will work to manage, oversee and may monitor /co- monitor clinical trial sites. **Essential...Education:** + Minimum of 4 years experience as a Clinical Research Associate in the… more
- Philips (San Diego, CA)
- …meetings. **You're the right fit if:** + You've acquired 2+ years of experience as a Clinical Research Associate ( CRA ), ideally within the medical device ... ** Clinical Research Associate -...informed consents, training materials, and device accountability logs. + Monitor clinical sites, track enrollment, verify source… more
- Philips (Norfolk, VA)
- … research in a fast-paced, impactful environment? Join Philips CMO as a Senior Clinical Research Associate ( CRA ) and help shape the future of ... nurse with experience in an ER-Pre Hospital/Hospital setting. Desired experience in clinical research , focused on the Emergency Care/ALS medical device/products.… more
- BeOne Medicines (San Mateo, CA)
- **General Description:** The SCRA is primarily a site monitor and is responsible for the management and oversight of their assigned clinical study sites to ... with Clinical Trial Oversight Managers (CTOMs) and Clinical Study Team (CST) to manage site ...audit/inspection findings to resolution as it related to involved CRA staff. * Assist with other assigned clinical… more
- Abbott (Alameda, CA)
- …the way people monitor their glucose levels with our new sensing technology. As the Clinical Research Associate I you will assist in the clinical ... execution and management of all aspects of assigned clinical studies. This includes but not limited to planning...Visits (SQV) and reporting to ensure study staff and research site are adequate to perform ADC… more
- University of Southern California (San Diego, CA)
- …understanding of study protocol and manuals. + Work closely with Lead Clinical Monitor /Lead CRA to escalate site compliance issues. + Participate in ... Clinical Research AssociateApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/San-Diego-CA/ Clinical - Research - Associate… more
- SUNY Upstate Medical University (Syracuse, NY)
- Job Summary: A Clinical Research Associate I will have a detailed understanding of each study protocol and background knowledge of the study medication and ... patients closely for any associated adverse events. + Maintain clinical research records; maintain files of approval...Interacts with investigators and their staff to facilitate and monitor the conduct of multidepartment clinical studies.… more
- Abbott (Alameda, CA)
- …degree in life sciences preferred or equivalent with minimum 2 years of clinical research experience, or combination of appropriate education and experience. + ... CRA will ensure quality, accuracy, and integrity of clinical trial data throughout the full lifecycle of multiple...track resolution of action items. + Assist and conduct clinical monitoring and site management activities, ensuring… more
- Edwards Lifesciences (Pittsburgh, PA)
- …us and be part of our inspiring journey. We are searching for a **Senior** ** Clinical Research Monitor ** to join Edwards Transcatheter Mitral and Tricuspid ... Therapies team. As the **Senior** ** Clinical Research Monitor ** , you...Clinical research certification (ACRP or SOCRA, Clinical Coordinator/ CRA certification) + Prior clinical… more
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