- Ochsner Health (Covington, LA)
- …bachelor's degree. Preferred - 2 years of experience in area of assigned clinical specialty, managing clinical research and patient databases. ... all documentation and regulatory submissions as required by the sponsor of the trial, regulatory agencies, research ...Skills and Abilities (KSAs)** + Knowledge of medical and clinical research terminology and processes. + Ability… 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
- Boehringer Ingelheim (St. Joseph, MO)
- …and benefit programs reflect Boehringer Ingelheim's high regard for our employees. The Clinical Research Associate (CRA) conducts in-house and external ... monitoring to verify that reported data collected in Clinical Lab Studies and Field Trials are accurate, complete,...Visits to evaluate qualifications of the site, Investigator, and research staff. + Conduct pre-study and ongoing monitoring visits… 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
- SUNY Upstate Medical University (Syracuse, NY)
- Job Summary: This position is responsible for the coordination of ALS clinical research studies. Performance of regulatory tasks including IRB and sponsor ... data collection and entry into paper and electronic databases, maintenance of clinical research supply inventory, processing clinical trial billing… 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
- 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
- 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
- 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
- Fresenius Medical Center (Jersey City, NJ)
- …to act as a resource and provide on-going leadership and support to Clinical Research Assistant I, answering questions and providing assistance as needed ... + Conducts on the job training for Clinical Research Assistant I as requested +...and submitted in a timely manner to Frenova Renal Research , CRO, study sponsor or IRB as… more