Clinical Research Coordinator

Elite Clinical Network; Austin (TX); On-site; USD 50,000 - 70,000; Full time

Job summary

A leading clinical research organization in Austin, Texas, seeks a motivated Clinical Research Coordinator (CRC) to support clinical trials. Responsibilities include coordinating research activities, recruiting participants, and ensuring compliance with ethical standards. Candidates are preferred to have a Bachelor's degree in a health-related field and relevant certifications. The role requires excellent organizational skills and the ability to work independently as part of a team. Offering competitive salary and full-time in-person work schedule.

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 day-to-day clinical research activities.
• Recruit, screen, and enroll study participants.
• Obtain informed consent and ensure ethical conduct.
• Collect, process, and ship biological specimens.
• Maintain accurate documentation in case report forms.
• Communicate with sponsors, monitors, and IRBs.

Skills

Organizational skills

Interpersonal skills

Communication skills

Proficiency in Microsoft Office

Experience with electronic data capture systems

Education

Bachelor's degree in a health-related field

Tools

REDCap

Job description

Job Summary

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