Clinical Research Coordinator

Flourish Research•Los Angeles, CA

24d•$31 - $43•Onsite

About The Position

Valkyrie Clinical Trials, a Flourish Research company, is hiring Clinical Research Coordinators at its Century City site. The Clinical Research Coordinator assists 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 excellent patient experience. The role is based at 2080 Century Pk E Suite 803, Los Angeles, CA 90067, and is scheduled Monday through Friday, 8:30 AM to 5:00 PM, with occasional weekends and overnights. Compensation is $31.00–$43.00 per hour depending on experience.

Requirements

Must have oncology clinical research experience.
Minimum of two years of clinical research experience.
A clear understanding of ICH, FDA, and GCP regulations.
Impeccable organizational skills and attention to detail.
Excellent communication and interpersonal skills for interacting with the Principal Investigator, research team, Study Sponsor/CROs, potential subjects, and referral sources.
An ethical, honest, detail-oriented, and self-driven approach to work.
High-level critical thinking skills.
Working knowledge of medical terminology and lab collection, processing, and storage procedures.
Proficiency with computers and Microsoft Office Suite.

Nice To Haves

Bachelor's degree preferred, but not required.
Clinical skills highly preferred, including vital signs, EKG/ECG, phlebotomy, and injections.
Familiarity with e-source reporting via an electronic platform.

Responsibilities

Execute protocol-specified patient visits and procedures, including tasks such as phlebotomy, IVs, injections, vital signs, and ECG/EKGs.
Document assessments and study data according to regulations and GCP, maintain complete source records, and accurately complete CRFs/eCRFs.
Obtain informed consent in accordance with federal regulations, GCP, and IRB requirements.
Ethically recruit qualified subjects to meet enrollment timelines.
Complete required and ongoing training, attend investigator meetings and courses, and stay current with changing regulations and Flourish policies.
Schedule and conduct visits according to protocol timelines.
Protect confidentiality in accordance with HIPAA and confidentiality agreements.
Report adverse events promptly; report serious adverse events to the sponsor within 24 hours and notify the PI/Sub-I/supervisor.
Account for and ensure availability of trial materials, including study drug, labs, CRFs, and supplies.
Maintain and document communication with Leads, Managers, PIs/Sub-Is, and the study team according to protocol and policy.
Perform duties safely and in a time- and cost-effective manner while complying with Flourish policies.
Represent Flourish professionally in all interactions.
Perform additional duties as assigned by management.