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Entry Level Clinical Research Associate Jobs in Spring, TX

Join a Team That's Advancing Clinical Research We're looking for a passionate and driven Clinical Research Associate (CRA) to join our team and play a key role in delivering high-quality clinical ...

Join a Team That's Advancing Clinical Research We're looking for a passionate and driven Clinical Research Associate (CRA) to join our team and play a key role in delivering high-quality clinical ...

Clinical Trial Technician

Houston, TX · On-site

$18.25 - $23.50/hr

The Clinical Trial Technician supports clinical research activities within the Leukemia department ... Research Assoc The University of Texas MD Anderson Cancer Center offers excellent benefits ...

New

Clinical Trial Technician

Houston, TX

$18.25 - $23.50/hr

The Clinical Trial Technician supports clinical research activities within the Leukemia department ... Research Assoc The University of Texas MD Anderson Cancer Center offers excellent benefits ...

New

Join a Team That's Advancing Clinical Research We're looking for a passionate and driven Clinical Research Associate (CRA) to join our team and play a key role in delivering high-quality clinical ...

Join a Team That's Advancing Clinical Research We're looking for a passionate and driven Clinical Research Associate (CRA) to join our team and play a key role in delivering high-quality clinical ...

Clinical Trial Technician

Houston, TX

$18.25 - $23.50/hr

The Clinical Trial Technician supports clinical research activities within the Leukemia department ... Research Assoc The University of Texas MD Anderson Cancer Center offers excellent benefits ...

New

Clinical Trial Technician

Houston, TX

$18.25 - $23.50/hr

The Clinical Trial Technician supports clinical research activities within the Leukemia department ... Research Assoc The University of Texas MD Anderson Cancer Center offers excellent benefits ...

New

Job Overview The Clinical Research Associate I (CRA I) plays a key role in supporting the successful conduct of clinical research studies by performing site monitoring and site management activities.

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Entry Level Clinical Research Associate information

What are the typical daily responsibilities of an Entry Level Clinical Research Associate?

As an Entry Level Clinical Research Associate, your day-to-day work generally involves assisting with monitoring clinical trial sites, reviewing study documentation, and ensuring adherence to protocol and regulatory requirements. You may support more senior team members in conducting on-site or remote visits, tracking patient recruitment, and managing data collection. Additionally, you’ll communicate regularly with site staff and other stakeholders to resolve issues and ensure data quality. This hands-on experience is essential for building expertise in clinical research processes and advancing toward more senior CRA roles.

What is an Entry Level Clinical Research Associate job?

An Entry Level Clinical Research Associate (CRA) is responsible for monitoring clinical trials to ensure compliance with regulatory requirements, ethical guidelines, and study protocols. They assist in site selection, data collection, and verifying that study procedures are properly followed. Entry-level CRAs typically work under the supervision of senior CRAs and may travel to different clinical sites. Strong attention to detail, knowledge of Good Clinical Practice (GCP) guidelines, and organizational skills are essential. This role is a starting point for a career in clinical research, with opportunities for growth into senior CRA or project management positions.

What are the key skills and qualifications needed to thrive in the Entry Level Clinical Research Associate position, and why are they important?

To thrive as an Entry Level Clinical Research Associate, you typically need a bachelor's degree in life sciences or a related field, a solid understanding of clinical trial protocols, and attention to detail. Familiarity with Good Clinical Practice (GCP) guidelines, electronic data capture (EDC) systems, and regulatory documentation is often required. Strong communication, organization, and problem-solving abilities help you effectively collaborate with study sites and team members. These skills are critical to ensure the accuracy, compliance, and successful progression of clinical studies.

What are popular job titles related to Entry Level Clinical Research Associate jobs in Spring, TX? For Entry Level Clinical Research Associate jobs in Spring, TX, the most frequently searched job titles are:
What job categories do people searching Entry Level Clinical Research Associate jobs in Spring, TX look for? The top searched job categories for Entry Level Clinical Research Associate jobs in Spring, TX are:
What cities near Spring, TX are hiring for Entry Level Clinical Research Associate jobs? Cities near Spring, TX with the most Entry Level Clinical Research Associate job openings:
Infographic showing various Entry Level Clinical Research Associate job openings in Spring, TX as of June 2026, with employment types broken down into 55% Full Time, 43% Part Time, and 2% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution.
Research Coordinator II - Pediatrics - Adolescent & Sports Medicine

Research Coordinator II - Pediatrics - Adolescent & Sports Medicine

Baylor College of Medicine

Houston, TX • On-site

$47K - $55K/yr

Full-time

Posted 2 days ago


Baylor College of Medicine rating

8.6

Company rating: 8.6 out of 10

Based on 21 frontline employees who took The Breakroom Quiz

51st of 537 rated colleges and universities


Job description

Job Title: Research Coordinator II - Pediatrics - Adolescent & Sports Medicine
Division: TCH Departments
Work Arrangement: Hybrid
Location: Houston, TX
Salary Range: $47,372 - $55,731
FLSA Status: Nonexempt
Work Schedule: Monday - Friday, 8 a.m. - 5 p.m.
Summary
This position participates in the development, implementation, and evaluation of health care transition programs.
Job Duties
  • Work closely with Senior Research Associate and other team members
  • Coordinate meetings, process meeting minutes for ongoing projects, and contact stakeholders to follow up on assigned tasks
  • Conduct literature reviews, use electronic reference management software to format manuscripts
  • Assist in submission of manuscripts through electronic portals
  • Collect data to track patients as they transition to adult care
  • Create and manage projects in REDCap, monitor data quality, conduct basic descriptive analyses
  • Develop and coordinate stakeholder feedback surveys and summarize results
  • Work with Division liaisons to identify potential project participants
  • Create recruitment flyers and patient education materials using design software
  • Conduct informed consent, in person or virtually, and securely file consent forms
  • Recruit participants to participate in research and quality improvement projects, coordinate interviews and survey distribution, and follow up with participants
  • Complete compensation form with participants and coordinate payment disbursements
  • Conduct chart reviews, data extraction and data management according to IRB protocols
  • Coordinate electronic correspondence
  • Assist with preparing IRB protocols, grants, abstracts, papers, posters, and other presentations
  • Complete all TCH and BCM periodic and annual training requirements, including but not limited to Epic and IRB
  • Assist with quarterly and annual reports
  • Assist with all administrative duties necessary to facilitate projects
  • Performs other job duties as assigned

Minimum Qualifications
  • Bachelor's degree in a related field. Four years of related experience may substitute for degree requirement.
  • One year of relevant experience.

Preferred Qualifications
  • Master's degree in Public Health, Health Sciences, Social Sciences, or a related field
  • Experience in clinical research, quality improvement, or healthcare program coordination
  • Familiarity with REDCap for database creation, management, and data quality monitoring
  • Experience conducting literature reviews and preparing manuscripts for publication
  • Basic data analysis skills using software such as Excel, SPSS, SAS, R, or similar tools
  • Knowledge of IRB processes, human subjects research, and regulatory compliance
  • Experience recruiting participants and obtaining informed consent in clinical or research settings
  • Strong organizational and project management skills with the ability to handle multiple tasks and deadlines
  • Experience creating recruitment materials or educational content using design tools (e.g., Canva, Adobe)
  • Excellent written and verbal communication skills, including interaction with diverse stakeholders
  • Ability to work both independently and collaboratively in a team-oriented environment
  • Familiarity with electronic medical records systems (e.g., Epic)
  • Experience supporting grant submissions, reports, abstracts, or presentations

Work Authorization Requirement:
This position is not eligible for visa sponsorship. Candidates must be legally authorized to work in the United States at the time of application and throughout the duration of employment.
Baylor College of Medicine is an Equal Opportunity/Affirmative Action/Equal Access Employer.
Requisition ID: 25467

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