Impactful Clinical Research Coordinator | Mission-Driven Growth

Elevate Clinical Research; Santee (CA); On-site; USD 34,000 - 48,000; Full time

Job summary

Elevate Clinical Research is seeking a Clinical Research Coordinator to manage the day-to-day operations of clinical trials, including patient recruitment, consent, and visits, while ensuring regulatory compliance across the study lifecycle.

The ideal candidate has 2+ years of coordination experience and familiarity with GCP, IRB processes, and regulatory documents. Join a mission-driven team delivering high-quality trials across multiple states.

Qualifications

• Bachelor’s degree in a health-related field such as Nursing, Life Sciences, or Public Health.
• At least 2 years of experience coordinating clinical research studies or trials.
• Comprehensive knowledge of clinical trial processes, regulatory requirements, and ethical standards.
• Familiarity with clinical research documentation, including informed consent forms and case report forms.
• Strong organizational skills and attention to detail to manage multiple study activities simultaneously.

Responsibilities

• Coordinate and oversee the daily operations of clinical trials, including patient recruitment, informed consent, and scheduling study visits.
• Ensure compliance with all regulatory requirements, institutional policies, and Good Clinical Practice (GCP) guidelines throughout the study lifecycle.
• Maintain accurate and up-to-date regulatory documents, case report forms, and study databases to support data integrity and audit readiness.
• Monitor study progress and patient safety by conducting regular assessments and reporting adverse events to the appropriate parties.
• Collaborate with investigators, sponsors, and multidisciplinary teams to facilitate effective communication and resolve study-related issues promptly.

Skills

Clinical trials coordination

Regulatory document management

Patient recruitment

Education

Bachelor’s degree in a health-related field

Master’s degree in Clinical Research or Public Health

Tools

EDC systems

CTMS

Job description

Elevate Clinical Research is seeking a Clinical Research Coordinator to manage the day-to-day operations of clinical trials, including patient recruitment, consent, and visits, while ensuring regulatory compliance across the study lifecycle.

The ideal candidate has 2+ years of coordination experience and familiarity with GCP, IRB processes, and regulatory documents. Join a mission-driven team delivering high-quality trials across multiple states.