Clinical Research Assistant Jobs in Dallas, TX
Clinical Research Assistant jobs in Dallas are in active demand, concentrated in the Uptown Medical District, Southwestern Medical District, and Frisco corridors, with strong hiring across clinical trial management, oncology, and cardiovascular research. Employers actively listing openings include UT Southwestern Medical Center, Fortrea, and Adams Clinical. Find a role that fits below and apply directly.
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Summary:
The Clinical Research Coordinator I (CRC) supports the conduct of clinical trials by coordinating study visits, managing data collection, and ensuring compliance with protocols and regulatory guidelines. This role involves direct interaction with participants including monitoring the health of each participant throughout the trial. The CRC plays a key part in maintaining study integrity and quality and collaborating with the Principal Investigator (PI) to provide oversight of the study to ensure adherence to Good Clinical Practice (GCP) guidelines.
Essential Duties and Responsibilities:
- Communicate clearly and professionally with study participants regarding study objectives and ongoing instructions.
- Adhere to site standard operating procedures (SOPs).
- Administer questionnaires and monitor participant compliance with study protocols.
- Respond to participant needs promptly and appropriately.
- Collect and document patient medical history and health conditions.
- Obtain and document informed consent from study participants.
- Maintain accurate records of investigational product (IP) dispensation and accountability.
- Coordinate with laboratories to ensure timely testing and reporting.
- Collect and document information on concomitant medications.
- Review medical records for protocol compliance.
- Perform and document assessments for adverse events (AEs) and serious adverse events (SAEs).
- Conduct clinical procedures including EKGs, vital signs, nasal swabs, and other protocol-specific tasks.
- Review clinical laboratory reports in accordance with protocol requirements.
- Maintain up-to-date regulatory files for the research site.
- Verify the accuracy and completeness of collected data.
- Monitor and document temperatures for IP storage.
- Support recruitment and engagement of study participants as needed.
- Develop electronic source (eSource) documents in accordance with study protocols.
- Manage study startup documentation, training, and timelines for assigned protocols.
- Ensure all protocol requirements and deadlines are met consistently.
- Maintain strict confidentiality and compliance with regulatory standards.
- Assist with preparation for monitoring visits.
- Enter data into electronic data capture (EDC) systems and resolve data queries.
- Perform other duties as assigned.
Qualifications:
- Minimum of 2 years of experience with phlebotomy and EKG procedures, with a current Certified Phlebotomy Technician (CPT) license required.
- Associate’s degree in healthcare or a related field, or equivalent relevant experience.
- Minimum of 2 years of experience in a healthcare setting.
- Minimum of 2 years of experience with FDA regulations and Good Clinical Practice (GCP).
- Demonstrated analytical reasoning skills.
- Exceptional attention to detail and strong organizational skills.
- Excellent verbal and written communication abilities.
- Proven customer service skills with both internal and external stakeholders.
- Ability to effectively manage multiple priorities in a fast-paced environment.
ACN does not provide visa sponsorship for this role. Candidates who will require immigration or visa sponsorship at any time now or in the future (including, but not limited to, H‑1B, TN, or STEM OPT training plans) are not eligible for this role.
About the Company:
At Alliance Clinical Network, our mission is to advance medical research by enrolling diverse populations in high-quality clinical trials. We are committed to maintaining the highest standards of integrity and excellence, and to ensuring that every participant receives respectful and compassionate care. We strive to build a tightly knit, supportive and collaborative environment where our team members can thrive and make meaningful contributions to human health.
Summary:
The Clinical Research Coordinator I (CRC) supports the conduct of clinical trials by coordinating study visits, managing data collection, and ensuring compliance with protocols and regulatory guidelines. This role involves direct interaction with participants including monitoring the health of each participant throughout the trial. The CRC plays a key part in maintaining study integrity and quality and collaborating with the Principal Investigator (PI) to provide oversight of the study to ensure adherence to Good Clinical Practice (GCP) guidelines.
Essential Duties and Responsibilities:
- Communicate clearly and professionally with study participants regarding study objectives and ongoing instructions.
- Adhere to site standard operating procedures (SOPs).
- Administer questionnaires and monitor participant compliance with study protocols.
- Respond to participant needs promptly and appropriately.
- Collect and document patient medical history and health conditions.
- Obtain and document informed consent from study participants.
- Maintain accurate records of investigational product (IP) dispensation and accountability.
- Coordinate with laboratories to ensure timely testing and reporting.
- Collect and document information on concomitant medications.
- Review medical records for protocol compliance.
- Perform and document assessments for adverse events (AEs) and serious adverse events (SAEs).
- Conduct clinical procedures including EKGs, vital signs, nasal swabs, and other protocol-specific tasks.
- Review clinical laboratory reports in accordance with protocol requirements.
- Maintain up-to-date regulatory files for the research site.
- Verify the accuracy and completeness of collected data.
- Monitor and document temperatures for IP storage.
- Support recruitment and engagement of study participants as needed.
- Develop electronic source (eSource) documents in accordance with study protocols.
- Manage study startup documentation, training, and timelines for assigned protocols.
- Ensure all protocol requirements and deadlines are met consistently.
- Maintain strict confidentiality and compliance with regulatory standards.
- Assist with preparation for monitoring visits.
- Enter data into electronic data capture (EDC) systems and resolve data queries.
- Perform other duties as assigned.
Qualifications:
- Minimum of 2 years of experience with phlebotomy and EKG procedures, with a current Certified Phlebotomy Technician (CPT) license required.
- Associate’s degree in healthcare or a related field, or equivalent relevant experience.
- Minimum of 2 years of experience in a healthcare setting.
- Minimum of 2 years of experience with FDA regulations and Good Clinical Practice (GCP).
- Demonstrated analytical reasoning skills.
- Exceptional attention to detail and strong organizational skills.
- Excellent verbal and written communication abilities.
- Proven customer service skills with both internal and external stakeholders.
- Ability to effectively manage multiple priorities in a fast-paced environment.
ACN does not provide visa sponsorship for this role. Candidates who will require immigration or visa sponsorship at any time now or in the future (including, but not limited to, H‑1B, TN, or STEM OPT training plans) are not eligible for this role.
About the Company:
At Alliance Clinical Network, our mission is to advance medical research by enrolling diverse populations in high-quality clinical trials. We are committed to maintaining the highest standards of integrity and excellence, and to ensuring that every participant receives respectful and compassionate care. We strive to build a tightly knit, supportive and collaborative environment where our team members can thrive and make meaningful contributions to human health.
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Find JobsClinical Research Assistant Job Market in Dallas
Who's Hiring
- UT Southwestern Medical Center108
- Fortrea29
- Adams Clinical8
- Tenet Healthcare8
- Alliance Clinical Network8
Top Industries Hiring
- Education41
- Agriculture & Farming4
- Healthcare & Medical Services4
Clinical Research Assistant Jobs in Dallas: Frequently Asked Questions
How do I get a clinical research assistant job in Dallas?
Focus your search on the Southwestern Medical District, where UT Southwestern Medical Center anchors a dense cluster of academic research programs, and on the hospital networks along the Uptown and Medical City corridors. Dallas also has a growing contract research organization presence in Frisco and Irving. Candidates who stand out typically have hands-on IRB documentation experience, familiarity with 21 CFR Part 11 compliance, and exposure to electronic data capture systems used in Phase II or III trials.
Which companies hire clinical research assistants in Dallas?
Employers hiring clinical research assistants in Dallas right now include UT Southwestern Medical Center, Fortrea, and Adams Clinical, based on current listings on Migrate Mate as of September 2026. Dallas draws a mix of large academic medical centers, regional hospital systems, and contract research organizations that support multi-site trials across the North Texas market.
Are there remote clinical research assistant jobs in Dallas?
Yes, though with limits: hands-on roles requiring patient interaction, sample processing, or on-site data collection are nearly always in-person. About 42% of clinical research assistant openings tied to Dallas are remote or hybrid as of September 2026, with most flexible arrangements concentrated in regulatory affairs support, data entry coordination, and sponsor-facing documentation tasks tied to Dallas-area trial sites.
How can I get a clinical research assistant job in Dallas with little or no experience?
The most realistic entry path in Dallas is through research coordinator internships or volunteer positions at UT Southwestern, Parkland Health, or the Children's Health system, which regularly onboard entry-level candidates for administrative and data support roles. Contract research organizations operating in the Frisco and Las Colinas areas also hire research assistants at the associate level for document management and site coordination. A phlebotomy certification or prior clinical volunteering gives applicants a concrete edge in screening.
Which industries hire the most clinical research assistants in Dallas?
Most clinical research assistant openings in Dallas sit in Education, Agriculture & Farming, and Healthcare & Medical Services, per current listings on Migrate Mate as of September 2026. Dallas's concentration of major hospital systems, academic medical institutions in the Southwestern Medical District, and a growing life sciences corridor in the northern suburbs makes it a consistently active market for clinical research support roles.
See All 199+ Clinical Research Assistant Jobs in Dallas
Find roles in Dallas that match your experience and apply in just a few clicks.
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