Clinical Research Coordinator — Trials, Specimens & Compliance

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

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.