Find & Apply For Clinical Research Coordinator Jobs in Baytown, Texas

Clinical Research Coordinator I Neutra Life Sciences Baytown, TX Job Details Full-time $18 - $25 an hour 9 hours ago Benefits Paid holidays Paid time off Qualifications Research laboratory experience Spanish Electronic health records (EHR) management Professional ethics Regulatory compliance English Clinic experience Phlebotomy specimen handling Productivity software Clinical confidentiality policies Full Job Description OB/GYN Clinical Research Coordinator I —

Baytown, TX Women's Healthcare Center of Baytown Schedule:

Full-Time, Monday-Friday, standard business hours

Location:

Women's Healthcare Center of Baytown, Baytown, TX Reports to:

Site Director Pay:

$18.00-$25.00 per hour, based on relevant clinical and research experience. Candidates without direct clinical research experience start at the lower end of the range; full training is provided as you build toward independent competency.

Work Authorization:

Must be authorized to work in the United States. NLS is unable to sponsor work visas for this position

Position Type:

Early-Career to Mid-Level Clinical Research Role Position Overview We are seeking a motivated individual with healthcare experience to join our Clinical Research team at an OB/GYN research site in Baytown. This role is designed for healthcare personnel building toward a US clinical research or medical career. An IMG (International Medical Graduate) background is not required, but is preferred. You'll work on FDA-regulated OB/GYN trials, with structured exposure to Good Clinical Practice standards and hands-on patient-facing research. Key Responsibilities Under the supervision of the Principal Investigator and the

Site Manager:

Clinical & Patient-Facing Duties This is where you build hands-on GCP experience directly relevant to a US clinical or research career. Assist with subject screening, enrollment, and informed consent support in accordance with study protocols and delegated authority Conduct study visits including vital signs, ECGs, phlebotomy, and protocol-specific assessments Perform patient follow-ups and assist with adverse event documentation and reporting Support investigators during physical exams and study procedures as permitted by protocol and delegation logs Preparation, handling, storage, accountability, and administration of investigational products (IP) in accordance with study protocols Laboratory & Specimen Management Proper specimen handling protects data integrity and subject safety; a skill set that transfers directly to any clinical setting. Collect, process, label, centrifuge, store, and ship biological specimens per protocol, laboratory manuals, and IATA guidelines Maintain specimen accountability logs and ensure chain-of-custody compliance Coordinate courier pickups and laboratory communications Ensure proper documentation, inventory control, and temperature monitoring Data & Documentation Source documentation is the backbone of trial integrity; this is where auditable, regulator-facing skill is built. Accurately document all study-related activities in source documents and electronic systems Enter data into Electronic Data Capture systems and assist with query resolution Request, review, and organize external medical records relevant to study participation Ensure timely investigator sign-off on labs, reports, and study documentation Operational & Administrative Support Site operations experience demonstrates the organizational competency that clinical and residency programs look for. Support daily research operations, including visit scheduling, reminders, and subject tracking Assist with recruitment efforts and prescreening activities Maintain regulatory binders, study logs, and site files as delegated Uphold strict confidentiality and compliance with HIPAA, FDA, ICH-GCP, and sponsor requirements Additional Responsibilities Participate in study trainings, protocol reviews, and site meetings Perform additional research-related duties as assigned to support efficient site operations Required Qualifications Healthcare background required Strong interest in clinical research and U.S. healthcare systems Bilingual Spanish and English required Phlebotomy experience required Minimum 2 years of clinical experience in a healthcare, research, or hospital setting Proficiency with Microsoft Office, electronic health records, and web-based research platforms Strong organizational skills with exceptional attention to detail Excellent written and verbal communication skills Professional demeanor, reliability, and ethical judgment Ability to manage day-to-day tasks independently within structured protocols and delegated supervision Demonstrated understanding of patient confidentiality and regulatory compliance Authorized to work in the United States (no sponsorship available) Preferred Qualifications IMG background; medical degree (MD or equivalent) obtained outside the United States. Familiarity with

GCP, FDA

regulations, and clinical trial workflows Experience working with diverse patient populations Benefits Full-time employees scheduled for 30 or more hours per week are eligible for paid time off and paid holidays, effective the first day of the month following hire.

Job Type:

Full-time Pay:

$18.00 - $25.00 per hour

Benefits:

Paid time off

Experience:

Clinic:

2 years (Required)

Language:

Spanish (Required)

Work Location:

In person