Clinical Research Assistant

Flourish Research•Los Angeles, CA

18d•$20 - $28•Onsite

About The Position

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 for a Clinical Research Assistant opportunity at the Flourish Research site in Northridge, CA. The Clinical Research Assistant supports the Investigators in executing Phase I, II, III, and IV clinical research trials in accordance with Standard Operating Procedures (SOPs), FDA and GCP guidelines, and study protocols while providing an impeccable patient experience in every single interaction. Shift: Monday - Friday, 8 AM - 5 PM Location: 18433 Roscoe Blvd #208, Northridge, CA 91325 Compensation: $20.00-$28.00/hr

Requirements

Experience performing phlebotomy with patients in a clinic or hospital setting
Familiar with e-source reporting via an electronic platform
A clear understanding of ICH, FDA, and GCP regulations
Impeccable organizational skills and attention to detail
Excellent communication and interpersonal skills to effectively interact with the Principal Investigator, 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

Nice To Haves

Experience with clinical research is preferred but not required

Responsibilities

Perform phlebotomy on clinical research participants and work directly with the site operations team to coordinate the trial process.
Assists in educating patients about the nature of their disease and the benefits and risks of participating in a clinical drug trial.
Determine protocol-related needs to conduct the trial and order supplies and equipment.
Recruits and screens potential patients and obtains informed consent.
Assists in providing patient education on the benefits and risks of participating in a clinical drug trial.
Designs source documents and forms to facilitate accurate data collection and recordkeeping.
Conducts in-service programs and summarizes study schedules to assist in understanding and implementing a protocol.
Schedules patient visits and laboratory and diagnostic test procedures.
Coordinates drug shipments, storage, and accountability.
Review trends, problems encountered, patient adverse events, and patient progress.
Perform other clinical skills as required by the trial protocol, including vital signs
Other responsibilites as assigned by leadership