Clinical Research Coordinator Assistant (CRCA)

at  Flourish Research

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.

QUALIFICATIONS

• 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
  Flourish Research offers an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities. Apply today to learn more about how you can join us in our mission to save and improve the lives of others!

• 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.