Clinical Trials Coordinator
2 weeks ago
Salary: $24 - $28 per hour; nonexempt
About Retina Consultants San Diego (RCSD)
Retina Consultants San Diego is a leading institution in innovative surgical procedures and clinical research, providing patients with access to cutting-edge retinal care and technology. Our team consists of board-certified retina specialists who are recognized leaders in their field, actively participating in professional organizations and contributing to advancements in retinal care.
Position Summary
The Clinical Research Coordinator (CRC) plays a vital role in the management of clinical trials, ensuring adherence to research protocols and regulatory requirements. The CRC collaborates with a multidisciplinary team, including investigators and research assistants, to facilitate the successful execution of clinical studies.
Key Responsibilities
- Thoroughly review and understand research protocols.
- Collect essential regulatory documents for study initiation.
- Maintain updated investigator credentials, including CVs and medical licenses.
- Gather financial disclosure forms and GCP certificates from all participating investigators.
- Ensure compliance with all regulatory requirements and documentation.
- Coordinate with the Principal Investigator and other team members to manage patient enrollment and study procedures.
- Oversee the care of 10-20 patients participating in clinical trials, ensuring adherence to study protocols.
- Assist in recruiting potential study subjects and conducting preliminary screenings.
- Conduct study-related procedures, including patient consent, blood draws, and medical history collection.
- Manage study-related inventory and ensure proper data collection and management.
- Collaborate with sponsors and monitors to ensure the integrity of research data.
- Adhere to privacy and confidentiality standards, as well as ICH-GCP and OSHA regulations.
- Assist in quality assurance activities to ensure high-quality data collection.
- Engage with the Institutional Review Board (IRB) for protocol amendments and reporting requirements.
- Contribute to study presentations and meetings as needed.
- Support fellow coordinators with patient management and regulatory tasks.
- Assist with financial documentation related to study activities.
- Perform other related duties as required.
Qualifications
- Proficient in computer applications, particularly Excel, Word, and Outlook.
- Certified Phlebotomy Technician (CPT) preferred for blood draw assistance.
- Strong communication skills, both written and verbal, to effectively document and discuss research activities.
- Excellent interpersonal skills to collaborate with diverse teams.
- Professional demeanor and respect for colleagues in a collaborative work environment.
Preferred Qualifications
- Experience or knowledge in Ophthalmology.
- Certification as a Certified Ophthalmic Assistant (COA) is a plus.
- Medical Assistant (MA) certification with patient care experience.
- Familiarity with laboratory procedures for specimen collection and processing.
- Certification as a Certified Clinical Research Coordinator (CCRC) is advantageous.
Benefits
- Competitive salary based on experience.
- Year-end bonus opportunities.
- Paid vacation days.
- Comprehensive medical, dental, vision, and life insurance benefits.
- 401K plan with employer matching contributions.
Work Environment
This is a full-time position with 8-hour shifts, Monday through Friday.
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