Research Assistant

Valkyrie Clinical Trials (VCT), a Flourish Research Company, is a leading Oncology multi-site clinical research network with expertise in Oncology research. VCT approaches clinical research with a deep sense of humanity, compassion, and sincere kindness. VCT was founded by leading Clinical Oncologist, Dr. David Berz, and has multiple sites spanning California in Century City, Panaroma City, and Murrieta, and has recently expanded to Denver, Colorado.

Flourish Research is one of the industry’s most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research. At Flourish Research, we strive toward excellence. In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status. We embrace employees, customers, and patients from these underrepresented groups to help make this vision a reality. Flourish is committed to a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect. The more diversity we have in our team, the more unique perspectives, and ideas we share, and the better prepared we are to serve our communities. WE SEE YOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU!

We are actively hiring a Research Assistant to support our Valkyrie Clinical Trials Century City, Los Angeles, CA site.

LOCATION: Onsite, Century City, Los Angeles, CA

FLSA: Non-Exempt

HOURS: Monday to Friday, Day Shift, 40 hours per week

COMPENSATION: $21.00 - $32.00 per hour (depending on experience)

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