Clinical Research Coordinator

ECN Operating LLC; Crystal City (MO); On-site; USD 50,000 - 70,000; Full time

Job summary

ECN Operating LLC is seeking a Clinical Research Coordinator (CRC) in Crystal City, Missouri, to manage various aspects of clinical trials. The CRC will handle participant recruitment, data collection, and regulatory compliance while ensuring adherence to ethical standards. Required qualifications include a Bachelor's degree in a health-related field and preferred certifications in Phlebotomy or as a Medical Assistant. Strong organizational and communication skills are essential, and proficiency in electronic data systems such as REDCap is desired.

Qualifications

• 1-2 years of experience in clinical research preferred.
• Phlebotomy certification or Medical Assistant certification preferred.
• Knowledge of Good Clinical Practice (GCP) and regulatory guidelines.

Responsibilities

• Coordinate clinical research activities to ensure protocols are followed.
• Recruit, screen, and enroll study participants.
• Maintain documentation in case report forms and electronic databases.

Skills

Organizational skills

Communication skills

Detail-oriented

Microsoft Office proficiency

Data collection

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.