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

Requirements

• Bachelor's degree preferred, but not required
• Clinical research experience is required, and oncology clinical research experience is preferred
• Minimum of two years of clinical research experience
• Clinical skills preferred: vital signs, EKG/ECG, phlebotomy, and injections
• 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