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Contract Research Associate Jobs in Spring, TX (NOW HIRING)

Exceptional research skills * Proficient computer skills: (including MS Word, MS Excel, PowerPoint ... Associates degree or paralegal certificate * Minimum of 3-5 years of contract/compliance ...

Exceptional research skills * Proficient computer skills: (including MS Word, MS Excel, PowerPoint ... Associates degree or paralegal certificate * Minimum of 3-5 years of contract/compliance ...

Excellent legal research, writing, and analytical skills. * Ability to work independently and ... Caleb Doyle Benefit offerings available for our associates include medical, dental, vision, life ...

Excellent legal research, writing, and analytical skills. * Ability to work independently and ... Caleb Doyle Benefit offerings available for our associates include medical, dental, vision, life ...

Research * Conduct legal research, using both Westlaw and Firm resources. * Summarize legal ... Draft various Contracts favoring client * Review and revise client-provided contracts Employment

Research Engineer

Houston, TX · On-site

$90K - $105K/yr

Collaborate with internal manufacturing partners, contract manufacturers, designers, and product ... Energetic with a clear sense of urgency and direction; able to inspire and invigorate associates at ...

Due to the nature of the government contract requirements and/or clearance requirements, US ... future research. Identify errors and areas for improvement in memos associated with these ...

Be Seen First

... contract disputes, and general civil litigation * Draft pleadings, motions, discovery responses ... Conduct legal research and develop case strategy with senior attorneys * Communicate directly with ...

Be Seen First

Manage litigation matters involving commercial litigation, contract disputes, premises liability ... Conduct legal research and develop case strategy with senior attorneys * Communicate directly with ...

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Contract Research Associate information

See Spring, TX salary details

$14

$28

$41

How much do contract research associate jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for contract research associate in Spring, TX is $28.96, according to ZipRecruiter salary data. Most workers in this role earn between $23.32 and $32.93 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Contract Research Associate, and why are they important?

To thrive as a Contract Research Associate, you need a solid background in life sciences or a related field, attention to detail, and experience with clinical research processes. Familiarity with regulatory systems like FDA guidelines, Good Clinical Practice (GCP), data management tools, and electronic data capture (EDC) systems is typically required. Strong organizational skills, effective communication, and the ability to work independently or in teams help set candidates apart. These competencies ensure that clinical trials are conducted accurately, compliantly, and efficiently, supporting successful research outcomes.

What is the difference between Contract Research Associate vs Clinical Research Coordinator?

AspectContract Research AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like CCRP beneficialBachelor's degree in health sciences or related field; certifications like CCRP or CCRC advantageous
Work EnvironmentTypically in pharmaceutical or biotech companies, contract research organizations (CROs)Usually in hospitals, clinics, or research sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, academic medical centers, research institutions
Common Search & ComparisonYesYes

While both roles support clinical trials, a Contract Research Associate primarily works for pharmaceutical or biotech companies managing trial processes remotely or at sites, often on a contractual basis. A Clinical Research Coordinator typically works directly at research sites, coordinating patient visits and data collection. Both roles require similar credentials and certifications, but their work environments and employer types differ.

What are some typical challenges faced by Contract Research Associates when managing multiple studies simultaneously?

Contract Research Associates often juggle several clinical trials at once, which can pose challenges in time management and prioritization. Balancing the requirements of different sponsors, adhering to varying protocols, and ensuring accurate documentation for each study demand strong organizational skills. Additionally, staying up to date with regulatory changes and effective communication with site staff are crucial to avoid delays and ensure compliance. Developing efficient workflows and leveraging project management tools can help address these challenges.

What is a Contract Research Associate?

A Contract Research Associate (CRA) is a professional who is typically hired on a contractual basis to support and manage clinical trials or research projects. Their primary responsibilities include monitoring research sites, ensuring compliance with protocols and regulations, collecting and verifying data, and maintaining proper documentation. CRAs play a critical role in ensuring the integrity and safety of clinical studies, often working for pharmaceutical companies, contract research organizations (CROs), or academic institutions. The contract nature of the role means that assignments are usually project-based and may vary in duration and scope.
What job categories do people searching Contract Research Associate jobs in Spring, TX look for? The top searched job categories for Contract Research Associate jobs in Spring, TX are:
What cities near Spring, TX are hiring for Contract Research Associate jobs? Cities near Spring, TX with the most Contract Research Associate job openings:
Research Billing Compl Anly - Research Administration - 004

Research Billing Compl Anly - Research Administration - 004

Texas Children's Hospital

Houston, TX • On-site

Full-time

Posted 4 days ago


Texas Children's Hospital rating

8.4

Company rating: 8.4 out of 10

Based on 171 frontline employees who took The Breakroom Quiz

62nd of 995 rated hospitals


Job description

We're looking for a Research Billing Compliance Analyst, someone who's ready to grow with our company. In this position, you'll be responsible for reviewing and processing clinical research billing activities for clinical trials and other clinical research studies. This role tracks and reviews clinical research billing grids and reviews pre-billed and billed charges related to clinical research. This role interacts with clinical research study teams, IS-EPIC, and other team members to reduce the risk of inappropriately billing patients and/or third parties for research related services/procedures.

Think you've got what it takes?

Job Duties & Responsibilities

Communicates effectively across various teams, including Clinical Trial Managers, Office of IRB, Academic Office of Clinical Research, Grants and Contracts, Internal Audit, Institutional Billing, and Hospital Finance

Receives initial protocol packages from Principal Investigators

May attend feasibility meetings

Communicates with the Principal Investigator, research nurses, and study coordinators to discuss study design and determine which items are standard of care versus research care

Works closely with Senior Billing Compliance Analysts and BCM's Office of Research to ensure the accuracy of billing grids

Completes timely pricing quotes for clinical trials and studies conducted at TCH within institutional and Medicare guidelines

Collects financial data (both manually and automatically) from several institutional databases and systems

Uses spreadsheets and database software to analyze charge, cost, and collection data for patients participating in clinical trials

Prepares monthly statements and invoices for review and payment by the Principal Investigator for clinical research charges per study

Maintains spreadsheets of study accounts and write-offs sent to Financial Services and Patient Accounting for institutional processing and tracking

Maintains and updates clinical trials in the Epic system (online medical record system)

Processes and reviews clinical research charges in Epic for both technical and professional charges

Accesses institutional charge masters to provide pricing for procedures using both SIMS and CPT codes

Accesses BRAIN to ensure the accuracy of IRB protocol information and verify approval

Accesses the Clinical Trials Management System (CTMS) to ensure appropriate billing modifiers are used on billing grids

Conducts clinical research billing audits of study records upon request or as needed.

Participates in cross-training with other staff on the Research Billing Compliance team

Learns FDA device regulations, CMS billing guidelines, and appropriate billing rules for various populations

Conducts and completes special projects as assigned and defined by the Assistant Director and/or Director within established timelines determined at project inception and by project participants and circumstances

Develops budgets for sponsors

Skills & Requirements

Bachelor's Degree Business or Hospital Administration or a related field required

CPC - Certified Professional Coder, American Academy of Professional Coders preferred

RHIA - Registered Health Information Administrator, American Health Information Management Association preferred

RHIT - Registered Health Information Technician, American Health Information Management Association preferred

CCRP - Certified Clinical Research Professional, Society of Clinical Research Associates preferred

CRA - Certified Research Administrator, Research Administrators Certification Council preferred

1 year Experience in research, billing, compliance, finance or Health Care Administration preferred

Familiarity with clinical trial study design, coordination and/or management preferred 

Since 1954, Texas Children's has been leading the charge in patient care, education and research to accelerate health care for children and women around the world. When you love what you do, it truly shows in the smiles of our patient families, employees and our numerous accolades such as being consistently ranked as the best children's hospital in Texas, and among the top in the nation by U.S. News & World Report as well as recognition from Houston Business Journal as one of this city's Best Places to Work for ten consecutive years. 

Texas Children's comprehensive health care network includes our primary hospital in the Texas Medical Center with expertise in over 40 pediatric subspecialties; the Jan and Dan Duncan Neurological Research Institute (NRI); the Feigin Tower for pediatric research; Texas Children's Pavilion for Women, a comprehensive obstetrics/gynecology facility focusing on high-risk births; Texas Children's Hospital West Campus, a community hospital in suburban West Houston; Texas Children's Hospital The Woodlands, the first hospital devoted to children's care for communities north of Houston; and Texas Children's Hospital North Austin, the new state-of-the-art facility providing world-class pediatric and maternal care to Austin and Central Texas families. We have also created Texas Children's Health Plan, the nation's first HMO focused on children; Texas Children's Pediatrics, the largest pediatric primary care network in the country; Texas Children's Urgent Care clinics that specialize in after-hours care tailored specifically for children; and a global health program that is channeling care to children and women all over the world. Texas Children's Hospital is affiliated with Baylor College of Medicine, one of the largest, most diverse and successful pediatric programs in the nation. 

 To join our community of 15,000+ dedicated team members, visit texaschildrenspeople.org for career opportunities.

 Texas Children's is proud to be an equal opportunity employer. All applicants and employees are considered and evaluated for positions at Texas Children's without regard to mental or physical disability, race, color, religion, gender, national origin, age, genetic information, military or veteran status, sexual orientation, gender identity, marital status or any other protected Federal, State/Province or Local status unrelated to the performance of the work involved.


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