CRC

Clinical Research Coordinator - Salinas, CA

Schedule: Monday-Friday, 8-5

Pay: $20-$25/hour

The Clinical Research Coordinator (CRC) is responsible for coordinating and administering clinical trials under the direction of the Clinical Research Manager, the Principal Investigator, and the Medical Director. The CRC will develop, implement, and coordinate research and administrative procedures to successfully manage clinical trials. The CRC will perform diverse administrative duties requiring analysis, sound judgment, and a high level of knowledge of study-specific protocols.

Responsibilities:

• Conduct and manage all clinical trial activities by established research protocols and standards in compliance with all applicable laws, regulations, policies, and procedural requirements.
• Collect and maintain study data and required records of clinical trial activity including but not limited to source documentation, case report forms, drug dispensation records, and regulatory forms.
• Monitoring research participants to ensure adherence to study rules.
• Adhering to research regulatory standards and ethical standards.
• Maintaining detailed records of studies as per FDA guidelines, including things such as drug dispensation.
• Liaising with laboratories regarding findings.
• Participating in subject recruitment efforts.
• Ensuring that the necessary supplies and equipment for a study are in stock and working order.
• Engaging with subjects and understanding their concerns.
• Ensure that non-serious and serious adverse events are properly documented and reported.
• Screen all laboratory results when received and follow protocol procedure regarding abnormal results.
• Ensure all laboratory results are given to appropriate doctors for review of clinical significance, then file results in the patient study binder
• Submit patient reimbursement requests after the patient's participation in the protocol.
• Ensure the filing and maintenance of all regulatory documents.
• Collect, process, and ship blood/urine specimens at scheduled patient visits.
• Perform ECGs and obtain vital signs of patients.
• Schedule all patient research visits and procedures consistent with the protocol requirements.
• Complete and maintain case report forms per FDA guidelines and review them against the patient's medical record for completeness and accuracy.
• Administer questionnaires/diaries per protocol.
• Other duties as assigned.

Qualifications:

• 1-3 years of experience working in Clinical Research
• Bilingual in Spanish and English

Benefits:

401(k) Retirement Plan, multiple medical, dental and vision plan options, Short Term Disability Insurance, Life Insurance Plan, Weekly Pay, Paid Sick Time Offered in WA (1 hour of sick time for every 30 hours worked)