- IQVIA (Carlsbad, CA)
- …in lieu of degree. * In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, ie, Good Clinical Practice (GCP) and ... with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the… more
- IQVIA (Durham, NC)
- …in lieu of degree. * Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. * ie, Good Clinical Practice (GCP) ... with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the… more
- IQVIA (Parsippany, NJ)
- …and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. You should have: + A Bachelor's degree ... or at least three months of on-site monitoring experience. 2 years of clinical research coordinator experience strongly preferred. + Alternatively, you should… more
- IQVIA (Philadelphia, PA)
- …and owning local trial activites at the regional level._** **Additional Information** Associate Clinical Project Managers (aCPM)/Local Trial Managers are an ... - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements ie ICH GCP and relevant local laws,… more
- Rush University Medical Center (Chicago, IL)
- …the position. Offers may vary depending on the circumstances of each case. The Associate Clinical Research Coordinator will provide support and contribute to ... disability, veteran status, and other legally protected characteristics. **Position** Associate Clinical Research Coordinator **Location** US:IL:Chicago… more
- Rush University Medical Center (Chicago, IL)
- …disability, veteran status, and other legally protected characteristics. **Position** Associate Clinical Research Coordinator **Location** US:IL:Chicago ... on the circumstances of each case. **Job Summary:** The Clinical Research Coordinator I (CRC I) supports...events, and serious adverse events). 11. Work with PI(s), sponsor , compliance, clinical staff and/or manager to… more
- Hartford HealthCare (Hartford, CT)
- …to us. *Job Summary:* As a specialized research professional the Senior Clinical Research Associate (SrCRA) collaborates with the Principal Investigator ... these duties, the SrCRA works with the PI, department, sponsor , IRB and institution to support and provide guidance...all aspects of study activity as required of a Clinical Research Associate This is… more
- Stanford University (Stanford, CA)
- Clinical Research Coordinator Associate **School of Medicine, Stanford, California, United States** **New** Research Post Date 2 days ago Requisition # ... 107255 The Stanford Stroke Center is seeking a Clinical Research Coordinator Associate to...databases, and regulatory files. + Participate in monitoring visits, sponsor meetings, and regulatory audits, serving as the study… more
- SUNY Upstate Medical University (Syracuse, NY)
- Job Summary: The Clinical Research Associate I will be responsible for the coordination of clinical research studies within the Department of ... data collection and entry into paper and electronic databases. Maintenance of clinical research supply inventory, processing clinical trial billing… more
- Ochsner Health (New Orleans, LA)
- …status. **Knowledge Skills and Abilities (KSAs)** + Knowledge of medical and clinical research terminology and processes. + Familiarity with ICH guidelines ... High school diploma or equivalent. **Work Experience** Required - 1 year of relevant research or clinical experience, OR Bachelor's degree in life science or… 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 to ... ensure compliance with study protocols, regulations, and sponsor requirements. Be at the forefront of groundbreaking...from you! IQVIA is a leading global provider of clinical research services, commercial insights and healthcare… more
- SUNY Upstate Medical University (Syracuse, NY)
- Job Summary: Coordination of clinical research studies. Performance of regulatory tasks including IRB and sponsor /CRO regulatory correspondence. ... Data collection and entry into paper and electronic databases. Maintenance of clinical research supply inventory. Processing clinical trial billing… more
- University of Southern California (San Diego, CA)
- Clinical Research AssociateApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/San-Diego-CA/ Clinical - Research - Associate ... San Diego, California The USC Keck School of Medicine - Alzheimer Therapeutic Research Institute (ATRI), located in San Diego, California is an academic institute… more
- ICON Clinical Research (NC)
- As a Clinical Research Associate you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare ... primary point of contact between investigational sites and the sponsor + Conduct all types of site visits, including...work in United States without visa sponsorship + A clinical research professional with 2+ years of… more
- OhioHealth (Columbus, OH)
- … works in collaboration with the Principal Investigator (PI) to coordinate assigned clinical research studies in accordance with Good Clinical Practice ... regulations. This position performs basic day to day activities related to clinical research studies including: recruit and screen participants, obtains informed… more
- Guthrie (Sayre, PA)
- Position Summary: Coordinate multiple in-patient and out-patient clinical research protocols. Education/Experience: Required: An Associate 's degree in ... experience with study coordination, and documented training of good clinical research standards training preferred. The completion...IRB, and event management of patient follow-up visits. Submit research data to sponsor via the appropriate… more
- SUNY Upstate Medical University (Syracuse, NY)
- …of education and experience. SoCRA certified or ACRP certified Experience with clinical research protocols, knowledge of medical terminology, computer skills, ... for the clinical trial. Manage all aspects of the clinical trial at the Sponsor Level including but not limited to: Procuring study drug, site selection… more
- Cedars-Sinai (Los Angeles, CA)
- …year of experience as a clinical research coordinator or clinical research associate /assistant preferred. + Demonstrated ability to accurately ... team and contribute to groundbreaking research .** This position functions as a Clinical Research Coordinator providing support for clinical research … more
- Georgetown Univerisity (Washington, DC)
- …(eg, the study monitor appointed by the sponsor for each trial). The Associate Director and the Director of Clinical Trials rely on timely responses from ... to making a difference in the world. Requirements The Clinical Research Coordinator 2 (CRC2) is responsible...a daily basis, the CRC2 will report to the Associate Director of Clinical Trials. The CRC2...to the sponsor contact… more
- SUNY Upstate Medical University (Syracuse, NY)
- … trial. Duties include but are not limited to: coordinate all aspects of the clinical trial at the Sponsor Level including but not limited to: procuring study ... This role will act as the project manager for a large multi-site clinical trial where the clinical site is also the coordination center for the clinical… more