Research Coordinator Jobs

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Clinical Research Coordinator

Flourish Research•Los Angeles, CA
•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 scheduled Monday through Friday, 8:30 AM to 5:00 PM, with occasional weekends and overnights. The position is located at 2080 Century Pk E, Suite 803, Los Angeles, CA 90067. Compensation is $31.00–$43.00 per hour, depending on experience. The company describes its environment as supportive and collaborative and offers growth opportunities and a comprehensive benefits package. Flourish Research is an equal employment opportunity employer and complies with applicable reasonable-accommodation requirements.

Requirements

  • Must have oncology clinical research experience.
  • At least two years of clinical research experience.
  • A clear understanding of ICH, FDA, and GCP regulations.
  • Strong organizational skills and attention to detail.
  • Excellent communication and interpersonal skills to interact effectively with the Principal Investigator, research team, study sponsors/CROs, potential subjects, and referral sources.
  • Honesty, attention to detail, and self-direction.
  • 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 are 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, which may include phlebotomy, IVs, injections, vital signs, and ECG/EKGs.
  • Document assessments and study data in accordance with regulations and GCP, maintain complete source documentation, 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 in accordance with protocol timelines.
  • Protect confidentiality in accordance with HIPAA and confidentiality agreements.
  • Report AEs promptly; report SAEs to the sponsor within 24 hours and notify the PI, Sub-I, or supervisor.
  • Account for trial materials and ensure their availability, including study drug, labs, CRFs, and supplies.
  • Maintain and document communication with Leads, Managers, PIs/Sub-Is, and the study team in accordance with protocol and policy.
  • Perform duties safely and in a time- and cost-effective manner, in compliance with Flourish policies.
  • Represent Flourish professionally in all interactions.
  • Perform additional duties as assigned by management.

Benefits

  • Health insurance
  • Dental insurance
  • Vision insurance
  • 401(k) with a 100% employer match on the first 4% of employee contributions
  • Tuition reimbursement
  • Parental leave
  • Referral program
  • Employee assistance program
  • Life insurance
  • Disability insurance
  • 15 days of PTO, 8 paid holidays, and 2 floating holidays

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