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

Future Ventures

Clinical Research Associate

Austin, TX · On-site

$89 - $148/hr

As a Clinical Research Associate, you'll play a crucial role in pioneering groundbreaking clinical ... Verify the accuracy, completeness, and consistency of clinical trial data through source data ...

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DiaSorin

Clinical Research Associate

Austin, TX

Enrolment logs, Data Record Forms, Case Report Forms etc.) * Contribute to the writing of study ... Coordinate and track clinical supplies shipped and used at clinical sites. * Acquisition of ...

DiaSorin

Clinical Research Associate

Austin, TX · On-site

Enrolment logs, Data Record Forms, Case Report Forms etc.) * Contribute to the writing of study ... Coordinate and track clinical supplies shipped and used at clinical sites. * Acquisition of ...

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All JobsClinical Data Associate JobsClinical Data Associate Jobs in Leander, TX

Clinical Data Associate information

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$37

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How much do clinical data associate jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for clinical data associate in Leander, TX is $37.22, according to ZipRecruiter salary data. Most workers in this role earn between $28.03 and $37.21 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.

More about Clinical Data Associate jobs

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

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

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For Clinical Data Associate jobs in Leander, TX, the most frequently searched job titles are:

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

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

Clinical Data Associate jobs near you
Infographic showing various Clinical Data Associate job openings in Leander, TX as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, and 2% Contract. Highlights an 84% Physical, 4% Hybrid, and 12% Remote job distribution, with an average salary of $77,415 per year, or $37.2 per hour.

Clinical Research Assistant (Round Rock)

Austin Retina Associates

Round Rock, TX • On-site

$18 - $24/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 5 days ago

Austin Retina Associates rating

8.1

Company rating: 8.1 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

Job description

Clinical Research Assistant (Round Rock)
Are you a skilled ophthalmic technician and passionate about the advancement of Ophthalmology? Want to positively impact patients' lives? Are you eager to expand your clinical skill set and ophthalmic knowledge? If so, join our dedicated team for a stimulating, supportive, and rewarding environment where your passion for eye care will flourish. We're looking for individuals like you! Join our dedicated team at Austin Retina Associates, at the forefront of ophthalmic innovation. We are committed to advancing the understanding and treatment of retinal diseases through rigorous clinical research. As a Clinical Research Assistant focused on Retina-specific trials, you will play a crucial role in bringing cutting-edge therapies to patients. This position offers a unique opportunity to contribute directly to clinical trials that have the potential to transform vision care. You will collaborate with leading ophthalmologists and researchers in a dynamic and supportive environment, gaining invaluable experience in the complexities of clinical trial management within a specialized area of Ophthalmology.
Summary
Austin Retina Associates is seeking curious and patient-focused individuals for a Clinical Research Assistant role. Our ideal candidate is passionate about patient care and the administrative aspects of clinical research.
What We Offer
  • Market-based wages
  • Three weeks of PTO
  • 3% company 401k contribution - regardless of your contribution
  • Three options for health insurance - including a free option
  • A truly family-like culture where our leaders practice humility
Duties
  • Work closely with clinical research coordinators to assist with collecting data from research patients.
  • Perform all required training to be allowed to participate in specific study protocols as a research assistant, including GCP, IATA, and any required protocol-specific training modules.
  • Learn the details of each study protocol as dictated by their specific role in the study.
  • Train to become certified to perform refractions and vision testing.
  • Assist research coordinators with providing care for study patients during study visits as well as perform diagnostic testing, schedule their appointments and educate them regarding their retinal condition, available treatment options and details of each study protocol.
  • Assist research coordinators with data entry for multiple EDC (Electronic Data Capture) systems.
  • Communicate effectively with research coordinators to ensure high quality data is captured.
  • Capture OCT imaging for study patients.
  • Label, export and upload images via numerous reading center submission portals.
  • Other duties assigned.

Required Attributes
  • Demonstrate our core values: Serving with Compassion, Striving for Excellence, and Practicing Humility
  • Strong interpersonal skills (effective listening, clear communication, effective customer problem resolution, warm demeanor)
  • Ability to master multiple computer systems (data entry and data retrieval)
  • Knowledge of (or ability to learn) ophthalmology and retina terminology
  • Ability and willingness to perform venipunctures and process samples (training provided)
  • Bilingual preferred.
Position Details
  • Hourly pay (FLSA non-exempt, eligible for overtime)
  • Physical requirements: Frequent standing and sitting, ability to view patient images and operate imaging devices, frequent use of a computer terminal, near constant standing and walking, manual dexterity to operate ophthalmic equipment, lifting heavy equipment
  • Coordinators will be delegated to serve in various roles on 20+ trials
  • Pay range: $18 to $24 / hr (commensurate with experience)

Benefits!
In addition to making a difference for our patients, Austin Retina offers amazing benefits to make a difference for our Team including:
  • Free HSA Medical Health Plan and 2 Blue Cross/Blue Shield Health Plans with generous employer contributions
  • Dental & Vision Insurance
  • Company paid life and long term disability insurance
  • Employee Assistance Program company paid
  • 401k with automatic Employer contributions even if you don't contribute
  • Rewards & Recognition program
  • Discount gym program
  • Fun company events
  • Leadership development and Career pathways

Physical Requirements
Prolonged standing, walking, sitting up to 4 hours a day, talking and hearing both in person and
by telephone; use hands to finger, handle and feel objects or controls; reach with hands and
arms. Regularly required to stoop, kneel, bend, crouch and lift up to 40 pounds on occasion.
Specific vision abilities required by this job includes viewing multiple computer screens, close
vision, distance vision, depth perception, color vision and the ability to adjust focus. Viewing
images and operating computer devices constantly.

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