Clinical Research Coordinator

Elite Clinical Network; San Diego (CA); On-site; USD 28,000 - 33,000; Full time

Job summary

Elite Clinical Network in San Diego, CA seeks a highly organized Clinical Research Coordinator to support clinical trials and research studies in an in-person, full-time capacity. You will coordinate subject recruitment, data collection, regulatory compliance, and specimen handling under direction from the study team.

The role requires a Bachelor’s degree in a health-related field, 1–2 years of clinical research experience, and familiarity with GCP.

Qualifications

• Bachelor’s degree in a health-related field required.
• 1–2 years of clinical research experience preferred.
• Phlebotomy or MA certification preferred.
• Knowledge of GCP and regulatory guidelines.
• Excellent organizational and communication skills.

Responsibilities

• Coordinate day-to-day clinical research activities to ensure adherence to study protocols.
• Recruit, screen, and enroll study participants.
• Obtain informed consent and ensure ethical conduct.
• Collect, process, and ship biological specimens per protocol.
• Perform basic clinical procedures (e.g., vital signs, EKG) as certified.
• Maintain documentation in case report forms and electronic databases.
• Communicate with sponsors, monitors, and IRBs regarding progress and compliance.
• Schedule participant visits and ensure visit windows are met.
• Maintain regulatory documents and assist with IRB submissions.

Skills

Recruitment & enrollment

Data collection & management

Regulatory knowledge

Communication skills

Organizational skills

Team collaboration

Education

Bachelor's degree in a health-related field

Tools

REDCap

EDC platforms

Microsoft Office

Job description

We are seeking a highly organized and motivated Clinical Research Coordinator (CRC) to join our research team. The CRC will coordinate and support all aspects of clinical trials and research studies, including subject recruitment, data collection, regulatory compliance, and specimen handling. Candidates with current Phlebotomy certification or Medical Assistant (MA) certification are strongly preferred, as this role may include specimen collection and basic clinical procedures.

Key Responsibilities

• Coordinate day-to-day clinical research activities to ensure study protocols are followed.
• Recruit, screen, and enroll study participants.
• Obtain informed consent and ensure ethical conduct in all study interactions.
• Collect, process, and ship biological specimens per protocol (e.g., blood draws, urine samples).
• Perform basic clinical procedures as permitted by certification (e.g., vital signs, EKGs).
• Maintain accurate and timely documentation in case report forms and electronic databases.
• Communicate with sponsors, monitors, and IRBs regarding study progress and compliance.
• Schedule participant visits and follow-ups; ensure visit windows are met.
• Ensure proper storage, handling, and accountability of investigational products, if applicable.
• Maintain regulatory documents and assist with IRB submissions.

Qualifications

• Bachelor's degree in a health-related field required.
• At least 1-2 years of experience in clinical research preferred.
• Phlebotomy certification or MA certification preferred.
• Knowledge of Good Clinical Practice (GCP) and regulatory guidelines.
• Excellent organizational skills and attention to detail.
• Strong interpersonal and communication skills.
• Proficiency in Microsoft Office and electronic data capture systems (e.g., REDCap, EDC platforms).
• Ability to work independently and as part of a multidisciplinary team.

Preferred Qualifications

• Experience working in clinical trials, especially in a hospital or academic setting.
• Familiarity with IRB processes and clinical trial documentation.
• Bilingual skills (depending on patient population) may be a plus.

Job Type

Full-time

Work Location

In person

Schedule

• 8 hour shift
• Monday to Friday
• Weekends as needed

Pay Range

• $20-24/hr