Clinical Research Coordinator

5 days ago

Orange, California, United States Orange County Neuropsychiatric Rese Full time

Job Title: Clinical Research Coordinator

Job Summary:

We are seeking a highly skilled and detail-oriented Clinical Research Coordinator to join our team at Orange County Neuropsychiatric Research. The successful candidate will be responsible for the coordination and administration of clinical trials under the direction of the Principal Investigator and Scientific Director.

Duties and Responsibilities:

  • Perform study procedures in accordance with Good Clinical Practice (GCP) and study protocols.
  • Coordinate protocol-related research procedures, study visits, and follow-up care.
  • Organize and maintain paper and electronic study data in a complete and accurate manner.
  • Work closely with recruitment and pre-screening teams to meet study enrollment goals.
  • Adhere to an Institutional Review Board (IRB)-approved protocol.
  • Participate in the informed consent process of study subjects.
  • Support the safety of clinical research patients/research participants.
  • Maintain study source documents.
  • Report adverse events.
  • Educate subjects and family members on the protocol, study intervention, study drug, etc.
  • Comply with institutional policies, standard operating procedures (SOPs), and guidelines.
  • Complete case report forms (paper and electronic data capture) and address queries.
  • Facilitate study initiation, monitoring visits, and close-out activities.
  • Retain records/archive documents after study close-out.
  • Requires effective writing and communication skills, ability to work as part of a team, and ability to multitask.
  • Act as liaison for research subjects, investigators, IRBs, sponsors, and healthcare professionals.
  • Document investigational product (drug/device) accountability.

Qualifications:

  • Bachelor's Degree required; degree in Biology and/or Psychology field preferred.
  • Must be willing and able to work in a clinical setting involving a psychiatric/mentally disabled population.
  • Must have ability to read and understand clinical trial protocols.
  • Must have attention to detail and the ability to handle multiple tasks with precision.
  • Must be adept with computers.
  • Must possess excellent critical thinking skills.
  • Must have excellent interpersonal and communication skills and be a hardworking team player.
  • Must possess strong data management skills.
  • Familiarity with medical terminology/environment required.
  • Available for full-time onsite position (40 hours/week).

Estimated Salary: $65,000 - $85,000 per year.

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