- Astellas Pharma (Denver, CO)
- …on Astellas, please visit our website at www.astellas.com . **Purpose and Scope:** A Clinical Site Monitor serves as the primary contact point between ... to clinical trial delivery through consistent communication and support. The Clinical Site Monitor will partner with Clinical Trial Lead (CTL,)… 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
- 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
- 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
- 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
- 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
- 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
- Edwards Lifesciences (San Francisco, CA)
- …us and be part of our inspiring journey. We are searching for a **Senior Clinical Research Monitor ** to join Edwards Transcatheter Pulmonic Field Monitoring ... team. As the Senior Clinical Research Monitor , you will...Clinical Research certification (ACRP or SOCRA, Clinical Coordinator/ CRA certification) Adhere to all company… more
- Edwards Lifesciences (Des Moines, IA)
- …Join us and be part of our inspiring journey. We are searching for a **Senior Clinical Research Monitor ** to join Edwards Aortic Field Monitoring team. As a ... Senior Clinical Research Monitor , you ensure...Clinical research certification (ACRP or SOCRA, Clinical Coordinator/ CRA certification) + Prior clinical… more
- BioFire Diagnostics, LLC. (Salt Lake City, UT)
- …above activities to the Clinical Scientist or Clinical Research Associate + Own the above site administrative support process + Prepare the on- ... collaboratively with the Clinical Study Scientist and Clinical Research Associate , in conjunction...site documentation as per Good Clinical Practices (Investigator Study File - ISF) + Handle… more
- Pfizer (Pearl River, NY)
- …EudraCT, or Pfizer.com). + Provides protocol specific training to study team, investigators, clinical research associate , and others. + Interact with ... least 2 years of experience in + The pharmaceutical industry (biopharmaceutical industry or Clinical Research Organization) related to clinical research … more
- Hackensack Meridian Health (Hackensack, NJ)
- …Preferred:** + Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical ... and serve as a leader of positive change. The ** Clinical Research Nurse** is responsible for coordinating... finance personnel. + Prepares and assists for sponsor monitor site visits and ensures all supporting… more
- Hackensack Meridian Health (Hackensack, NJ)
- …Preferred:** + Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical ... and serve as a leader of** **positive change.** The ** Clinical Research Nurse** is responsible for coordinating... finance personnel + Prepares and assists for sponsor monitor site visits and ensures all supporting… more
- Bristol Myers Squibb (Madison, NJ)
- …other scientific field preferred) **Experience Requirements** + 5+ years of experience in clinical science, clinical research , or equivalent + Proficient ... applicable + Evaluate innovative trial designs (collaboration with Medical Monitor / Clinical Development Lead) + Protocol and ICF...CRO scope of work, etc. + Review development of site and CRA training materials and presentation… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …4 or More Years with PharmD/PhD preferred + Experience considered relevant includes clinical or basic research in a Pharmaceutical company, a Medical ... device/Diagnostic company, Academic Research Organization (ARO) or Contract Research Organization (CRO). preferred + CRA experience preferred + Time spent… more
- e CancerCare (Fresno, CA)
- …administrator, or physicians. Experience, Qualifications/Education: 3+ years of relevant experience as a clinical research associate or clinical ... the clinic practice site (s). Supervises staff, including Research Nurses, Clinical Research Coordinators,...study budgets with the assistance of the finance department. Monitor all study funds and revenues assuring that sponsor… more
- Community Health Network (Indianapolis, IN)
- …& CERTIFICATION REQUIREMENTS + within three (3) years from hire Certifications/Licensures: (Certified Clinical Research Associate (CCRA - ACRP), Certified ... Clinical Research Coordinator Job Ref 2503280...Communication: Communicates on a regular basis with the Investigators, Research Team, Hospital Staff, Monitor and other… 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
- Abbott (Alameda, CA)
- …+ BS degree in life sciences or equivalent with minimum 5 years of clinical research experience, or MS degree in life sciences or equivalent with ... their glucose levels with our new sensing technology. The CRA II will assist in the clinical ...minimum 3 years of clinical research experience, or Ph.D. with 2+… more
- ICON Clinical Research (New York, NY)
- …up and responding to clinical study specific inquiries from Sponsors, Physicians, CRA and CRO representatives and the ICON Site Services Department. * Review ... Project Manager, Laboratory ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive… more