at Actalent in Champaign, Illinois, United States
Job Description
Onsite Clinical Research Coordinator
Recruit and screen participants for clinical trials and maintain subject screening logs Perform vital signs, bloods draws/sample collections, ECGs, spirometry, dose verification, cannulation, and cardiac telemetry monitoring Collect, record, and maintain research subject study data according to study protocols and SOPs, preserving quality control for content, accuracy, and completeness Collect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical research Assist in the initial and ongoing consent process; orient research subjects to the study, including the purpose of the study, procedures, and research process Maintain source documentation based on protocol requirements Schedule and execute study visits and perform study procedures Handle lab testing and analysis, including preparation of specimen collection tubes, shipment, and lab logistics Monitor subject safety and report adverse events/reactions to the Principal Investigator and/or appropriate medical personnel Correspond with research subjects and troubleshoot study-related questions or issues Assist with study data quality checking and query resolution Assist investigator in verifying that research study objectives are met on time, within budget and according to applicable protocol requirements, clinical research regulations and quality standards Provide training to new investigator site staff members on study-specific topics and requirements Assist in maintaining adherence to investigator site staff training requirements by auditing and maintaining training records Prepare for and attend study monitoring visits, study audits, and regulatory inspections with clinical research regulatory agencies Assist research site with coverage planning related to staffing and scheduling for research studies Monitor subject safety and report adverse reactions to appropriate medical personnel Maintain confidentiality of data and PHI as required Maintains stock of supplies needed to carry out each study per protocol Performs other duties and projects as assignedQualifications
MUST have a minimum 1 year of Clinical Research Coordinator experience Experience with patient recruitment, patient enrollment, phlebotomy and other patient care skills Experience with EMR and EDC systems BS/BA in life sciences or educational equivalent High school diploma or General Education Development (GED) also acceptable with years of CRC experienceShift
Monday-Friday 8:00 AM-5:00 PMAbout Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & InclusionAt Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
+ Hiring diverse talent
+ Maintaining an inclusive environment through persistent self-reflection
+ Building a culture of care, engagement, and recognition with clear outcomes
+ Ensuring growth opportunities for our people
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.
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