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Clinical Data Associate Jobs in Oklahoma (NOW HIRING)

Through our unparalleled science, data, technology and laboratory network, we advance diagnostics ... Associate's degree in a Chemical or Biological science, Clinical Laboratory Science, Medical ...

Through our unparalleled science, data, technology and laboratory network, we advance diagnostics ... Associate's degree in a Chemical or Biological science, Clinical Laboratory Science, Medical ...

Associate's degree in a Chemical or Biological science, Clinical Laboratory Science, Medical ... Formore information about how we collect and store your personal data, please see ourPrivacy ...

Associate's degree in a Chemical or Biological science, Clinical Laboratory Science, Medical ... For more information about how we collect and store your personal data, please see our Privacy ...

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Clinical Data Associate information

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$12

$35

$80

How much do clinical data associate jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for clinical data associate in Oklahoma is $35.97, according to ZipRecruiter salary data. Most workers in this role earn between $27.07 and $35.96 per hour, depending on experience, location, and employer.

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 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 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 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 Oklahoma? The most popular types of Clinical Data jobs in Oklahoma are:
What are popular job titles related to Clinical Data Associate jobs in Oklahoma? For Clinical Data Associate jobs in Oklahoma, the most frequently searched job titles are:
What cities in Oklahoma are hiring for Clinical Data Associate jobs? Cities in Oklahoma with the most Clinical Data Associate job openings:
Infographic showing various Clinical Data Associate job openings in Oklahoma as of August 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 100% In-person job distribution, with an average salary of $74,809 per year, or $36 per hour.

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 11 days ago


Job description

We do more than treat cancer. Be a part of the most powerful team of cancer experts and advocates who invest in the health and well-being of our patients throughout treatment and beyond. As part of the team, you will be pursuing the most advanced, innovative, and cost-effective treatment options, so that our patients receive personalized, custom care best suited to their situation.

Under direct supervision, this position tracks a variety of information for all patients who are registered on approved clinical treatment protocols. Manages the reporting of data to company sponsors and other appropriate bodies. Maintains all research protocol data and compliance reporting. Performs all data management functions of the department. Supports and adheres to the Oklahoma Cancer Specialists and Research Institute Compliance Program, to include the Code of Ethics and Business Standards. Qualifications: High School diploma or equivalent required. An associate degree or bachelor’s degree preferred. Medical Assistant and/or LPN experience is highly desired. Two or more years of experience in Oncology/Research preferred. Ability to examine documents for accuracy and completeness required. Knowledge of medical terminology required. Knowledge of current FDA regulations, Good Clinical Practice, governing clinical research preferred. CCRP certification is preferred but not required.

Compensation is competitive and commensurate with experience, qualifications, and other relevant factors.

Oklahoma Cancer Specialists and Research Institute is an EEO employer. We offer an excellent Benefits Package which includes medical, dental, vision, voluntary benefits, 401k, paid time off (PTO) and 10 holidays per year.