Flourish Research is hiring: Clinical Research Assistant in Murrieta
Behavioral Health Market Context
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Benefits
Compensation: $21/hr - $32/hr, depending on experienceBenefits: Health, dental, and vision insurance plans, 401(k) with 4% match, tuition reimbursement, parental leave, referral program, employee assistance program, life insurance, disability insurance, and 15 days of PTO + 10 company holidaysFlourish Research offers an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities
Qualifications
- •Minimum of two years of clinical research experience
- •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
- •6 more items(s)
Responsibilities
- •The Clinical Research Assistant supports clinical research studies under the supervision of the Site Director or Clinical Research Coordinator
- •This role assists with clinic operations and study procedures across all phases of research, ensuring accurate data collection and compliance with GCP, IRB, and sponsor protocols while providing an impeccable patient experience in every, single interaction
- •Shift: Monday-Friday, 8:30 AM - 5 PM (occasional weekends)
- •Support CRCs and site staff with protocol-specified patient visits and procedures, which may include, but not limited to, phlebotomy, IVs, injections, vital signs, ECG/EKG, etc
- •Document assessments and study data per regs/GCP
- •Obtain and document informed consent following federal regulations and IRB guidelines
- •Support patient recruitment efforts and scheduling to meet enrollment goals
- •Maintain accurate source documentation and complete case report forms (CRFs)
- •Report adverse events to supervisors or investigators as needed
- •Help manage study supplies, lab kits, and other trial materials
- •Maintain confidentiality and follow all applicable compliance and ethical standards
- •Communicate effectively with research team members and document relevant study communications
- •Represent Flourish Research professionally in all interactions
- •Perform additional duties as assigned by management
- •11 more items(s)
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