Clinical Research Coordinator - Tyler, TX
Behavioral Health Market Context
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Benefits
The pay range for this position is $30.00 - $40.00/hrSubject to specific elections, plan, or program termsMedical, dental & visionCritical Illness, Accident, and Hospital401(k) Retirement Plan – Pre-tax and Roth post-tax contributions availableLife Insurance (Voluntary Life & AD&D for the employee and dependents)Short and long-term disabilityHealth Spending Account (HSA)Transportation benefitsEmployee Assistance ProgramTime Off/Leave (PTO, Vacation or Sick Leave)Ensuring growth opportunities for our people9 more items(s)
Qualifications
- •Must be bilingual in English and Spanish
- •Minimum of 2 years of CRC experience
- •Phlebotomy experience required
- •Strong organizational, prioritization, and leadership skills
- •Excellent knowledge of medical and research terminology
- •Knowledge of federal regulations and good clinical practices
- •Ability to operate independently for most study activities
- •Strong computer skills, including clinical trials database and electronic data capture
- •Maintaining an inclusive environment through persistent self-reflection
- •6 more items(s)
Responsibilities
- •The Clinical Research Coordinator plays a vital role in the screening, enrollment, and monitoring of clinical research study subjects while ensuring adherence to protocol and regulatory compliance
- •Utilizing Good Clinical Practices (GCP), this role is critical in maintaining high standards of patient care and study integrity
- •Prioritize activities with regard to protocol timelines
- •Ensure compliance with FDA regulations and ICH guidelines in all clinical trials
- •Maintain effective relationships with study participants and research personnel
- •Interact professionally with patients, sponsor representatives, and investigators
- •Coordinate and attend pre-study site visits, site initiation visits, and monitor visits
- •Identify adverse events and serious adverse events, notifying the Principal Investigator and Sponsor as appropriate
- •Prescreen study candidates and obtain informed consent in accordance with SOP
- •Complete visit procedures according to protocol, including training others in clinical procedures
- •Review laboratory results, ECGs, and test results for completeness and alert values
- •Discuss study medication, required procedures, eligibility criteria, and impact on office flow with investigators and site staff
- •Record data legibly and enter in real-time on paper or electronic source documents
- •Manage study medication inventory, dispensation, and patient compliance
- •Resolve data management queries and assist in regulatory document completion and filing
- •Building a culture of care, engagement, and recognition with clear outcomes
- •13 more items(s)
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