Research Jobs in Dallas, TX
Research jobs in Dallas are in strong and active demand, with openings concentrated in the Medical District, Uptown, and the Southwestern Medical District corridor across life sciences, healthcare, higher education, and corporate analytics. Employers hiring right now include UT Southwestern Medical Center, Baylor Scott & White Health, and Fortrea. 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 Research JobsResearch Job Market in Dallas
Who's Hiring
- UT Southwestern Medical Center378
- Baylor Scott & White Health10
- Fortrea3
- ICON3
- Alliance Clinical Network3
Top Industries Hiring
- Education
- Healthcare & Medical Services
Research Jobs in Dallas: Frequently Asked Questions
How do I get a research job in Dallas?
The strongest path into Dallas research is targeting the city's healthcare and life sciences corridor anchored around UT Southwestern Medical Center and Parkland Health, where clinical and laboratory research roles concentrate. Corporate research and analytics roles cluster in Uptown and Las Colinas. Candidates who can demonstrate data fluency, experience with IRB protocols, or published work gain a clear edge in Dallas's competitive and credential-driven market.
Which companies hire researchs in Dallas?
Companies currently hiring researchs in Dallas include UT Southwestern Medical Center, Baylor Scott & White Health, and Fortrea, per current listings on Migrate Mate as of September 2026. Dallas draws a mix of academic medical centers, large health systems, corporate headquarters, and independent research institutes, giving candidates a wide range of employer types to target.
Are there remote research jobs in Dallas?
Yes, though availability depends heavily on the type of research work, desk-based, analytical, or policy roles can often be done remotely, while laboratory, clinical, or field research almost always requires on-site presence. About 37% of research openings tied to Dallas are remote or hybrid as of September 2026. The most remote-friendly roles locally tend to be in market research, data analytics, and policy analysis.
How can I get a research job in Dallas with little or no experience?
The most realistic entry path in Dallas is a research assistant or research coordinator role at one of the city's academic medical institutions or large health systems, where structured training and supervision are built into the position. Universities in the area and corporate analytics teams in the Uptown and Frisco corridors also hire entry-level analysts. Familiarity with statistical software, strong writing skills, and a completed thesis or capstone project all strengthen local applications.
Which industries hire the most researchs in Dallas?
Dallas research roles concentrate in Education and Healthcare & Medical Services, based on current listings on Migrate Mate as of September 2026. Dallas's standing as a major healthcare hub and the presence of several Fortune 500 headquarters make those sectors the primary engines of local research hiring.
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