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Clinical Data Associate Jobs in Rosharon, TX (NOW HIRING)

This Clinical Data Abstracter position offers the opportunity to work with complex oncology ... Associate's Degree or College courses in medical terminology, anatomy or physiology. WORK ...

This Clinical Data Abstracter position offers the opportunity to work with complex oncology ... Associate's Degree or College courses in medical terminology, anatomy or physiology. WORK ...

This Clinical Data Abstracter position offers the opportunity to work with complex oncology ... Associate's Degree or College courses in medical terminology, anatomy or physiology. WORK ...

Clinical Affairs Scientist

Houston, TX · On-site +1

$105K - $197K/yr

... Associates, Quality Assurance, and Regulatory Affairs to assure compliance with internal and ... Design and develop databases, Electronic Data Capture (EDC) systems, and case report forms.

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Clinical Data Associate information

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How much do clinical data associate jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for clinical data associate in Rosharon, TX is $34.85, according to ZipRecruiter salary data. Most workers in this role earn between $26.25 and $34.86 per hour, depending on experience, location, and employer.

What does a clinical data associate do?

A Clinical Data Associate is responsible for collecting, validating, and managing clinical trial data to ensure its accuracy, completeness, and compliance with regulatory standards. They work closely with clinical research teams to monitor data quality, resolve discrepancies, and prepare data for analysis. Their work is essential in supporting drug development and regulatory submissions by ensuring reliable and high-quality clinical data.

What does a clinical data associate do?

A clinical data associate is responsible for tracking data and results in a research study. As a clinical data associate, your job duties are to collect data, perform data management, and input data into any software used by your team. You work on a research team, so you must be able to work collaboratively and have excellent organizational skills. While you spend most of your time in an office, you may be required to work in the field to record data. The only universal qualifications needed for this career are a background in health care or medical science research and experience with data management software like Oracle Clinical, Microsoft Excel, and SPSS.

What are the key skills and qualifications needed to thrive as a clinical data associate, and why are they important?

To thrive as a Clinical Data Associate, you need a solid understanding of clinical research, data management principles, and attention to detail, often supported by a degree in life sciences or a related field. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools, and knowledge of regulatory guidelines like GCP or CDISC is typically required. Strong organizational skills, analytical thinking, and clear communication set outstanding candidates apart in this role. These skills ensure the accuracy, integrity, and compliance of clinical trial data, which are crucial for successful research outcomes and regulatory approval.

What are some common challenges faced by clinical data associates when ensuring data quality during clinical trials?

Clinical Data Associates often encounter challenges such as identifying and resolving discrepancies in large datasets, maintaining strict compliance with regulatory standards, and coordinating timely data entry from multiple sites. They must work closely with clinical research teams and data managers to clarify ambiguous data and implement data cleaning procedures. Staying organized and detail-oriented is essential to ensure data accuracy and the successful progression of clinical trials.

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

AspectClinical Data AssociateClinical Research Coordinator
Primary RoleManage and ensure accuracy of clinical trial dataOversee trial operations, patient recruitment, and site management
CredentialsBachelor's in life sciences or related field; familiarity with data managementBachelor's in health sciences or related field; clinical trial experience
Work EnvironmentData management teams, clinical trial databasesClinical sites, hospitals, research facilities
Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical trial sites

While both roles support clinical trials, a Clinical Data Associate primarily focuses on managing and validating trial data, ensuring accuracy and compliance. In contrast, a Clinical Research Coordinator handles the overall trial operations, including patient recruitment and site coordination. Both roles require relevant certifications and work within the clinical research industry, but their daily responsibilities differ significantly.

What are the most commonly searched types of Clinical Data jobs in Rosharon, TX?

The most popular types of Clinical Data jobs in Rosharon, TX are:

What job categories do people searching Clinical Data Associate jobs in Rosharon, TX look for?

The top searched job categories for Clinical Data Associate jobs in Rosharon, TX are:

What cities near Rosharon, TX are hiring for Clinical Data Associate jobs?

Cities near Rosharon, TX with the most Clinical Data Associate job openings:

Clinical Data Abstracter

MD Anderson

Houston, TX • On-site, Remote

Full-time

Medical, Dental, Retirement, PTO

Posted 4 days ago


MD Anderson Cancer Center rating

8.5

Company rating: 8.5 out of 10

Based on 172 frontline employees who took The Breakroom Quiz

14th of 891 rated healthcare providers


Job description

The Cancer Registry department at MD Anderson Cancer Center plays an essential role in maintaining accurate, comprehensive cancer data that supports patient care, cancer surveillance, regulatory reporting, research, and institutional quality initiatives. The team carefully reviews patient medical records to capture critical information about cancer diagnoses, treatment, and disease characteristics while ensuring data meets applicable regulatory and state requirements.
This Clinical Data Abstracter position offers the opportunity to work with complex oncology information and contribute to the accuracy of cancer data used throughout MD Anderson. The role is ideal for a highly detail-oriented professional who enjoys reviewing medical records, interpreting clinical information, and working independently to ensure information is captured accurately and consistently.
In this role, you will review detailed and complex patient medical records, including handwritten and electronic documentation, to identify and abstract malignant and benign disease information. Key data elements may include cancer site, histology, stage, and other clinical oncology information required to meet regulatory and state reporting requirements.
You will also support case finding activities by identifying cancer cases within Epic and completing minimal data abstraction for research and operational purposes. The ability to navigate medical records, recognize relevant oncology information, and accurately distinguish information that should be captured will be important to success in this role.
A major focus of the position is data quality and accuracy. You will be responsible for maintaining a high level of quality in abstracted information through careful review and attention to detail. Abstracted data may be evaluated through coworker review, user feedback, and other quality mechanisms, making consistency and exacting accuracy essential.
The ideal candidate will be highly detail-oriented, organized, comfortable working with complex medical information, and capable of maintaining accuracy while reviewing large amounts of documentation. Candidates who enjoy medical record review, data abstraction, and working with oncology information will find this opportunity especially rewarding.
MD Anderson offers a comprehensive total rewards package, including paid medical benefits, generous paid time off, retirement plans, tuition assistance, professional development opportunities, and additional benefits, along with the opportunity to build a rewarding career at one of the world's leading cancer centers while contributing to cancer surveillance, research, regulatory reporting, and the advancement of oncology care.
This position is remote within Texas only
Abstracting - Read and comprehend detailed and complex medical information, either handwritten or typed, from patient medical records. Information to abstract meets regulatory agencies and state requirements and includes malignant and/or benign disease information (i.e. cancer site, histology and stage) Responsible for abstracting non-analytical (failed treatment) cases and minimal clinical oncologic data elements.
Case Finding - Identify cancer cases in Epic and do a minimal data abstraction for research and operational purposes.
Abstracting Quality - Maintain high quality of abstracted data as determined by co-worker review, user feedback, and other data-review mechanisms. Demonstrate attention to detail as exacting accuracy of abstracted information is essential.
EDUCATION
Required: High School Diploma or Equivalent
Preferred: Associate's Degree or College courses in medical terminology, anatomy or physiology.
WORK EXPERIENCE
Required: 2 years Experience in tumor registry, healthcare or related field.
May substitute required education degree with additional years of equivalent experience on a one to one basis.
LICENSES AND CERTIFICATIONS
Preferred: CTR - Cert Tumor Registrar Upon Hire
The University of Texas MD Anderson Cancer Center offers excellent benefits, including medical, dental, paid time off, retirement, tuition benefits, educational opportunities, and individual and team recognition.
This position may be responsible for maintaining the security and integrity of critical infrastructure, as defined in Section 113.001(2) of the Texas Business and Commerce Code and therefore may require routine reviews and screening. The ability to satisfy and maintain all requirements necessary to ensure the continued security and integrity of such infrastructure is a condition of hire and continued employment.
It is the policy of The University of Texas MD Anderson Cancer Center to provide equal employment opportunity without regard to race, color, religion, age, national origin, sex, gender, sexual orientation, gender identity/expression, disability, protected veteran status, genetic information, or any other basis protected by institutional policy or by federal, state, or local laws unless such distinction is required by law.http://www.mdanderson.org/about-us/legal-and-policy/legal-statements/eeo-affirmative-action.html
Additional Information
  • Requisition ID: 182518
  • Employment Status: Full-Time
  • Employee Status: Regular
  • Work Week: Days
  • Minimum Salary: US Dollar (USD) 43,000
  • Midpoint Salary: US Dollar (USD) 54,000
  • Maximum Salary : US Dollar (USD) 65,000
  • FLSA: non-exempt and eligible for overtime pay
  • Fund Type: Hard
  • Work Location: Remote (within Texas only)
  • Pivotal Position: No
  • Referral Bonus Available?: No
  • Relocation Assistance Available?: No

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