Clinical Research Coord, I

Responsibilities

• Under direct supervision of the Director of Clinical Operations, Manager of Clinical Operations and principal investigator, the CRC 1 is responsible for enlisting, maintaining, and assuring protocol compliance for all study participants in clinical trials
• Collaborates with study investigator in determining eligibility of potential participants in clinical trials
• Screens potential participants for protocol eligibility. Presents trial concepts and details to the participant, participates in the informed consent process, and enrolls participants in study protocol
• Ensures research quality by practicing in compliance with Standard Operating Procedures (SOP), principles of Good Clinical Practice (GCP) and applicable federal, state, and local regulations
• Coordinates patient care in compliance with protocol requirements. May disburse investigational drug and provide participants’ education regarding medication administration. Maintains investigational drug accountability, when needed, in cases where the Research Pharmacy is not maintaining that responsibility
• In collaboration with the study investigator, reviews study participants for changes in condition, adverse events, concomitant medication use, protocol compliance, response to study drug and thoroughly documents all findings
• Responsible for accurate and timely data collection, documentation, entry, and reporting. Schedules and participates in monitoring and auditing activities
• Maintains current and accurate documentation in the regulatory binder(s) as required by regulations and sponsors
• Participates in required training and education programs. Responsible for education of other personnel and vendors regarding clinical research
• Provide a safe environment for study participants, caregivers, and study personnel at all times through compliance with all federal, state, and professional regulatory standards. Maintains strict patient confidentiality according to HIPAA regulations and applicable law
• Participates in the after-hours support and coverage schedule, if necessary
• Be at work and be on time
• Interact in a positive and constructive manner
• Follow company policies, procedures and directives

Preferred

• Knowledge of clinical trial federal, state and local regulation requirements preferred
• Bachelor's degree in relevant field preferred
• Research certification (e.g. ACRP, SoCRA or equivalent) preferred
• Phlebotomy certification preferred
• Current CITI training preferred

Benefits

• After-hours Support Staff will be compensated for his/her time providing support during these after hours.
• In addition to base pay, there may be additional compensation available for this role, including but not limited to, shift differentials, extra shift incentives, and bonus opportunities.
• High quality health insurance plan options, so you can select the best choice for your family.
• Glassdoor
• 4.1
• MemorialCare is a healthcare firm that provides joint replacement, blood donation, sports medicine, primary, and surgical care services.
• Fountain Valley, California, USA
• https://www.memorialcare.org
• Late Stage
• Leadership Team
• Barry Arbuckle
• Chief Executive Officer
• Recent News
• PR Newswire
• MemorialCare Expands Advanced Thoracic Surgery Program with Addition of Matthew D. Stanley, M.D.
• 2026-09-11
• Hoda Assadian Named Chief Operating Officer for MemorialCare's Long Beach Medical Center and Miller Children's & Women's Hospital
• 2026-08-10
• AVIA Recognizes MemorialCare for Outstanding Innovation in Digital Transformation for the Third Year in a Row
• 2026-06-05
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Qualifications

• Minimum of two (2) years of clinical research experience required
• Excellent interpersonal and communication skills required
• Ability to read and understand clinical trial protocols required
• Strong data management skills and attention to detail required
• Familiarity with medical terminology/environment required
• Extensive knowledge of Microsoft Office (Word, Excel, and Adobe Acrobat) required
• Associates degree or equivalent education required
• Knowledge of clinical trial federal, state and local regulation requirements preferred
• Bachelor's degree in relevant field preferred
• Research certification (e.g. ACRP, SoCRA or equivalent) preferred
• Phlebotomy certification preferred
• Current CITI training preferred
• Minimum of two (2) years of clinical research experience required.

Required skills

• ACRP Certification, Adobe Acrobat, CITI Training, Clinical Research, Clinical Trial Protocols, Clinical Trial Regulations, Data Management, Medical Terminology, Microsoft Excel, Microsoft Word, Phlebotomy Certification, SoCRA Certification

Preferred skills

• Bachelor's degree in relevant field preferred, Current CITI training preferred, Phlebotomy certification preferred

Experience

• 2+ years