Clinical Research Coordinator, Level 1

Perform technical and clinical requirements of study protocols, including venipuncture, specimen processing, vital signs, electrocardiograms, IV infusions, IV pump operations, Holter monitoring, pulmonary function testing, allergy testing, pregnancy testing, strep throat screening, and injections or other protocol-required procedures Attend investigator meetings, site initiation visits, and coordinator meetings for protocol and clinical procedure training Obtain knowledge of study drugs, especially injection and intravenous infusion medications Monitor for possible complications during study-drug administration Maintain accurate dispensing logs with lot number, drug/placebo, and mixer/preparer information Document laboratory data and adverse reactions and notify investigators, sponsors, and the Institutional Review Board of unexpected or serious events when indicated Recruit suitable patient participants and promote the service to monitors, sponsor representatives, and in-house contacts Respond to queries, enter data promptly, and work with monitors during onsite visits Prepare study documentation for sponsor or FDA audits and assist auditors Order clinical supplies and manage protocol-specific rescue drugs Maintain code/crash cart and AED assessments and documentation Monitor refrigerators, freezers, and investigational-product storage temperatures Maintain knowledge of temperature-monitoring devices and laboratory specimen and investigational-product procedures Maintain dry-ice packaging and shipping certification and support laboratory workflow Act as the site OSHA Representative, including maintaining immunization records, obtaining vaccines, and administering staff vaccines Perform equipment calibration when needed and maintain calibration records Support clinical-skills training and development for site staff Assist other staff according to organizational needs and priorities May travel to other local Duly Health & Care sites within the Accellacare network Requirements 1+ years of work experience in a clinical research or pharmaceutical environment Strong attention to detail Motivation for a career in clinical research Excellent time management and planning skills with an organized approach to work Bachelor's degree in life sciences or another related field Legal right to work in the country where the role is based Maintain certification for packaging and shipping specimens on dry ice Maintain OSHA Representative responsibilities and related immunization records Core Competencies Demonstrates expertise in clinical research protocols, including venipuncture, specimen processing, and monitoring study-drug administration. Maintains compliance with regulatory standards and effectively manages clinical supplies and documentation. Highest-signal resume keywords Clinical Research Experience Venipuncture Skills Attention To Detail Time Management OSHA Representative Responsibilities ATS Optimization Keywords Hard Skills Specimen Processing Vital Signs Monitoring Electrocardiograms IV Infusions Holter Monitoring Pulmonary Function Testing Adverse Reaction Documentation Equipment Calibration Temperature Monitoring Study Protocol Compliance Soft Skills Strong Attention To Detail Excellent Time Management Organizational Skills Motivation For Clinical Research Certifications & Qualifications Dry Ice Packaging And Shipping Certification Industry Keywords Clinical Research Pharmaceutical Environment Study Protocols Investigator Meetings FDA Audits Tools & Technologies Temperature-Monitoring Devices IV Pumps Crash Cart AED #J-18808-Ljbffr Jobtailor