Clinical Trials Coordinator

The Clinical Research Coordinator (CRC): Is responsible for providing support for clinical research protocols. In addition, assist with all clinical research aspects at selected satellite sites. This individual will interact with subjects, the clinic, research staff, laboratory staff, and medical professionals. The CRC must be able to jump in and help in a busy environment. Supports clinical research activities for assigned research projects. Recruit subjects for participation in studies, facilitate patient care, prepare the case report form (CRF), submit CRFs and other data to the Sponsor as necessary, and study close-out under the main office Anaheim's guidance, CA. Reviews protocols and informed consent forms for completeness and compliance with regulations.

Responsibilities/Duties:

• Conducting research and patient visits with Principal Investigator. Pre-screening/Patient Follow-up.
• Maintain scheduling pre-study testing, treatments, outside labs, scans, biopsies, and other tests for all clinical research visits under the main office's guidance.
• Maintains appropriate records of clinical activities and other duties as assigned.
• Provide support (including administrative/clerical) and information to subjects, staff, and external sources related to current research projects.
• Preparing and updating patient charts.
• EDC Data Entry/ Query Resolution.
• Assembles lab kits and other supplies in preparation to obtain required biospecimen samples and transports to appropriate laboratories for processing; ships samples externally according to IATA requirements.
• Attend meetings and conferences related to research activities.

Qualifications:

• MS, MA, MD or MD-equivalent (preferred not required)
• Experience in a field that includes patient assessments, such as psychology (preferred)
• Excellent communication skills (interpersonal, written, and verbal).

Experience/Skills:
Experience in the field of clinical research is required. Knowledge of clinical trial federal, state and local regulatory requirements preferred.
Must know about Google Suite programs, computer skills, ability to conduct Internet searches. Knowledge of OpenClinica and OpenEMR (preferred).
Strong project management, analytical, organizational, and problem-solving skills. Superior interpersonal and communication skills. Demonstrated ability to work on deadlines, set priorities, and juggle multiple projects without compromising quality. Detail-oriented and highly organized.

Job Type: Full-time

Pay: $23.00 - $30.00 per hour

Benefits:

• 401(k)
• Health insurance
• Paid time off

License/Certification:

• GCP (Preferred)

Work Location: In person