Clinical Research Coordinator

ECN Operating LLC; Katy (TX); On-site; USD 52,000 - 72,000; Full time

Job summary

ECN Operating LLC in Texas is seeking a Clinical Research Coordinator to support all aspects of clinical trials, including recruitment, data collection, regulatory compliance, and specimen handling. The CRC will coordinate day-to-day activities, obtain informed consent, manage schedule visits, and ensure proper documentation in CRFs and electronic systems such as REDCap.

Candidates with Phlebotomy or MA cert are preferred; bachelor's in health field required; 1–2 years' experience and strong

Qualifications

• Bachelor's degree in a health-related field is required.
• 1–2 years of clinical research experience preferred.
• GCP knowledge and regulatory guidelines are expected.

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.
• Perform basic clinical procedures as certified (e.g., vitals, EKGs).
• Maintain accurate documentation in CRFs and electronic data capture systems.
• Communicate with sponsors, monitors, and IRBs regarding progress and compliance.
• Schedule participant visits and manage visit windows.

Skills

Organizational skills

Interpersonal communication

Attention to detail

Team collaboration

Independent work

Education

Bachelor's degree in a health-related field

Tools

REDCap

EDC platforms

Microsoft Office

Job description

Career Opportunities with ECN Operating LLC

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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.