Clinical Research Coordinator

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 Coordinators at our Century City, Los Angeles site location.

This is one of our three oncology research sites in the Greater Los Angeles area.

These locations are formerly Valkyrie Clinical Trials - we are proud to welcome Valkyrie Clinical Trials to the Flourish Research network!

The Clinical Research Coordinator assists 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 : 30 AM - 5 PM (occasional weekends) Location :   2080 Century Park E, Suite 803, Los Angeles, CA 90067 Compensation :   $72,000 - $79,000 ($34.60 - $37.98 / hr) Benefits :   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 holidays.
• RESPONSIBILITIES Execute 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; maintain complete source; accurately complete CRFs / eCRFs.
• Obtain informed consent per federal regs, GCP, and IRB requirements.
• Ethically recruit qualified subjects to meet enrollment timelines.
• Complete required / ongoing training; attend investigator meetings / courses; stay current with changing regulations and Flourish policies.
• Schedule and conduct visits per protocol timelines.
• Protect confidentiality per HIPAA and all confidentiality agreements.
• Report AEs promptly; report SAEs to sponsor within 24 hours and notify PI / Sub-I / supervisor.
• Account for and ensure availability of trial materials (study drug, labs, CRFs, supplies).
• Maintain and document communication with Leads, Managers, PIs / Sub-Is, and study team per protocol and policy.
• Perform duties safely, and in a time- / cost-effective manner compliant with Flourish policies.
• Represent Flourish professionally in all interactions.
• Additional duties as assigned by management.

QUALIFICATIONS Bachelor's degree preferred, but not required Must have oncology clinical research experience Minimum of two years of clinical research experience Clinical skills highly preferred :

Apply today to learn more about how you can join us in our mission to save and improve the lives of others!