Clinical Research Coordinator Assistant (CRCA)

Flourish Research•San Antonio, TX

3d•$21•Onsite

About The Position

This is an excellent opportunity for those with clinical experience who want to enter the clinical research industry! Flourish Research is looking for motivated, talented, creative individuals who want to learn and grow in their careers while contributing to research that changes lives! We offer an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities. We are actively hiring Clinical Research Coordinator Assistants at our Clinical Trials of Texas site in San Antonio! The Clinical Research Coordinator Assistant is critical in supporting the Clinical Research Coordinators and the research team in providing an impeccable patient experience in every interaction. Your role will include a variety of tasks, from patient recruitment, source documentation, data entry, and direct patient interaction during site visits. Shift: Monday-Friday, 8:30 AM - 5 PM Location: 5430 Fredericksburg Rd., Suite 200, San Antonio, TX 78229 Compensation: Up to $21/hr Benefits: Health, dental, and vision insurance plans, 401(k) with a 100% employer match on the first 4% of employee contributions, tuition reimbursement, parental leave, referral program, employee assistance program, life insurance, disability insurance, and 15 days of PTO + 8 paid holidays and 2 floating holidays. CRCAs have a clear path to promotion into a Clinical Research Coordinator position!

Requirements

Bachelor's degree preferred but not required
Must have either clinical research experience OR clinical skills, such as taking vitals, phlebotomy, EKGs, etc
Impeccable organizational skills, attention to detail, and people skills, as you will be interacting directly with patients
Excellent communication and interpersonal skills to effectively interact with the Principal Investigator, CRCs, other members of the research team, Study Sponsor/CROs, potential subjects, and referral sources
An ethical compass that compels the candidate to be honest, detail-oriented, and self-driven
High-level critical thinking skills
Working knowledge of medical terminology and lab collection/processing/storage procedures
Proficiency with computers and Microsoft Office Suite

Responsibilities

Assist in the recruitment, screening, and enrollment of study participants.
Coordinate and manage the scheduling of trials and maintain communication with participants.
Collect, organize, and process clinical data from trials.
Maintain source documentation from patient visits and protocol activities
Work alongside clinical research coordinators to conduct patient visits.
Once trained, perform phlebotomy, EKGs, and/or other diagnostic procedures as needed
Learn, understand, and comply with rules and regulations governing medical ethics, IRB, GCP, and ICH guidelines
Provide administrative support to research staff by organizing meetings, preparing reports, and maintaining records.
Additional duties as assigned by management.