Clinical Research Coordinator

ECN Operating LLC; San Diego (CA); On-site; USD 50,000 - 70,000; Full time

Job summary

ECN Operating LLC in San Diego, California is seeking a Clinical Research Coordinator (CRC) to join their research team. This role involves coordinating and supporting clinical trials including subject recruitment and data collection. A Bachelor’s degree in a health-related field, along with 1-2 years of clinical research experience, is required. Phlebotomy or Medical Assistant certification is preferred. The position demands excellent organizational and communication skills, and familiarity with Good Clinical Practice (GCP).

Qualifications

• 1-2 years of experience in clinical research preferred.
• Phlebotomy certification or MA certification strongly preferred.
• Knowledge of regulatory guidelines.

Responsibilities

• Coordinate day-to-day clinical research activities.
• Recruit and enroll study participants.
• Collect and process biological specimens.

Skills

Excellent organizational skills

Strong interpersonal skills

Proficiency in Microsoft Office

Knowledge of Good Clinical Practice

Ability to work independently

Education

Bachelor's degree in a health-related field

Tools

REDCap

EDC platforms

Job description

Clinical Research Coordinator (CRC)

We are seeking a highly organized and motivated 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.