Clinical Research Coordinator - 247696

Medix™; Austin (TX); On-site; USD 45,460 - 50,971; Full time

Benefits offered by this job

Medical insurance

Vision insurance

401(k)

Job summary

A leading healthcare solutions provider in Austin, Texas is seeking a Clinical Research Coordinator for a full-time, 6-month contract position which may transition into a permanent role based on performance. Responsibilities include coordinating clinical trials, ensuring compliance with regulations, and maintaining accurate study records. Ideal candidates will have experience in clinical research, particularly in weight loss, diabetes, or endocrinology studies. The position is 100% on-site.

Qualifications

• Strong background in clinical research coordination.
• Experience managing clinical trials and regulatory compliance.
• Excellent communication skills.

Responsibilities

• Coordinate and manage all aspects of assigned clinical trials.
• Conduct study visits and maintain study records.
• Support regulatory compliance and participate in audits.

Skills

Clinical Research Coordinator experience

Experience with weight loss, diabetes or endocrinology studies

Data entry and management

Tools

eSource systems

eConsent

eISF

Job description

This range is provided by Medix™. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$33.00/hr - $37.00/hr

Looking for a strong Clinical Research Coordinator to join our team!

• This is a 6 month contract to hire (based off performance/attendance)
• Must have Clinical Research Coordinator experience
• Experience with weight loss, diabetes or endocrinology studies

Start Date: December 1st

100% onsite!!!

Clinical Trial Coordination

• Coordinate and manage all aspects of assigned Phase 2–4 clinical trials from site initiation to close-out.
• Conduct study visits, including obtaining informed consent, performing protocol-required procedures, and collecting source data using eSource systems.
• Ensure timely and accurate entry of study data into electronic case report forms (eCRFs).
• Utilize eSource, eConsent, eISF, and other clinical trial software platforms to maintain complete, accurate, and regulatory-compliant study records.
• Support site readiness and compliance with 21 CFR Part 11, ICH GCP, and sponsor SOPs.

Regulatory Compliance

• Maintain up-to-date regulatory documents and study binders (electronic and/or paper as required).
• Assist with preparation for sponsor, CRO, or regulatory audits.
• Recruit, screen, and enroll study participants according to protocol inclusion/exclusion criteria.
• Ensure ongoing patient safety by monitoring for adverse events and reporting per protocol.
• Serve as the primary point of contact for sponsors, CROs, monitors, and other site staff.

Support training and mentoring of new CRC staff as assigned.

• Provide on-site support at additional study locations when required (occasional travel).

Seniority Level

Associate

Employment Type

Full-time

Job Function

Research

Industries

Hospitals and Health Care

Referrals increase your chances of interviewing at Medix™ by 2x

Benefits

• Medical insurance
• Vision insurance
• 401(k)

We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.