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 assigned
Qualifications
MUST live in the area or willing to relocate at own cost (no relocation offered)
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 experience
ShiftMonday-Friday 8:00 AM-5:00 PM About 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 & Inclusion At 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.
