Research Coordinator Jobs in Dallas, TX
Research Coordinator jobs in Dallas are in strong demand, concentrated in the Medical District, Uptown, and the Southwestern Medical District corridor across clinical research, academic medicine, and life sciences. Employers hiring right now include UT Southwestern Medical Center, Alliance Clinical Network, and IntraCare. Scan the live roles below and apply to whichever ones fit.
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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.
See All 114+ Research Coordinator Jobs in Dallas
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Find Research Coordinator JobsResearch Coordinator Job Market in Dallas
Who's Hiring
- UT Southwestern Medical Center60
- Alliance Clinical Network12
- IntraCare6
- Wake Research6
- Adams Clinical6
Top Industries Hiring
- Education
Research Coordinator Jobs in Dallas: Frequently Asked Questions
How do I get a research coordinator job in Dallas?
Target Dallas's dense clinical and academic research ecosystem first. UT Southwestern Medical Center, Parkland Health, and Children's Health anchor a Medical District corridor that consistently posts coordinator openings, and the surrounding life sciences and biotech firms in the Southwestern Medical District add more. Candidates with clinical trial experience, IRB familiarity, or a background in public health have a clear edge over general applicants in this market.
Which companies hire research coordinators in Dallas?
Employers hiring research coordinators in Dallas right now include UT Southwestern Medical Center, Alliance Clinical Network, and IntraCare, based on current listings on Migrate Mate as of September 2026. Dallas draws a mix of large academic medical centers, regional health systems, pharmaceutical companies, and contract research organizations, all of which staff coordinator roles at multiple levels.
Are there remote research coordinator jobs in Dallas?
Yes, though availability depends heavily on the role type. Hands-on clinical and lab-based coordinator positions almost always require on-site presence, while data coordination, survey research, and administrative protocol roles are far more remote-friendly. About 27% of research coordinator openings tied to Dallas are remote or hybrid as of September 2026, with the remote share concentrated in health services research and non-laboratory academic positions.
How can I get a research coordinator job in Dallas with little or no experience?
The most realistic entry path in Dallas is through a research assistant or clinical trials assistant role at one of the Medical District institutions, which regularly hire early-career candidates. UT Southwestern and Parkland Health both run research programs that bring on entry-level staff. A background in biology, public health, or nursing, combined with familiarity with electronic data capture systems, makes candidates competitive for these junior openings even without prior coordinator experience.
Which industries hire the most research coordinators in Dallas?
Dallas research coordinator roles concentrate in Education, based on current listings on Migrate Mate as of September 2026. The city's size as a regional medical hub, combined with a growing biotech and pharmaceutical presence near the Southwestern Medical District, keeps demand across these sectors consistently high.
See All 114+ Research Coordinator Jobs in Dallas
Find roles in Dallas that match your experience and apply in just a few clicks.
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