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Research Study Jobs in Dallas, TX (NOW HIRING)

2505

Clinical Research Coordinator II

Dallas, TX · On-site

$24 - $32/hr

Collects and ensures quality control of clinical or basic research data in support of multiple and/or complex research studies. BENEFITS UT Southwestern is proud to offer a competitive and ...

2505

Clinical Research Coordinator II, Neurology

Dallas, TX · On-site

$24 - $32/hr

The Clinical Research Coordinator II is responsible for independently coordinating and managing clinical research studies with minimal supervision. This position requires at least two years of ...

2504

Clinical Research Coordinator I

Dallas, TX

$24 - $32/hr

Collects and ensures quality control of clinical or basic research data in support of multiple and/or complex research studies. BENEFITS UT Southwestern is proud to offer a competitive and ...

2504

Clinical Research Coordinator I

Dallas, TX · On-site

$24 - $32/hr

Collects and ensures quality control of clinical or basic research data in support of multiple and/or complex research studies. BENEFITS UT Southwestern is proud to offer a competitive and ...

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Research Study information

What is a research study?

A Research Study job involves conducting investigations to gather, analyze, and interpret data on a specific topic. Professionals in this role design experiments, collect information from various sources, and summarize findings to contribute to scientific or academic knowledge. They may work in universities, healthcare, corporate research, or government agencies. Responsibilities can include literature reviews, data collection, statistical analysis, and report writing.

What are the typical daily responsibilities of someone working in a research study role?

Daily responsibilities in a Research Study role often include collecting and managing data, recruiting and coordinating with study participants, and maintaining accurate documentation of research activities. You may also be involved in designing study protocols alongside lead researchers, analyzing results using statistical software, and preparing progress reports or manuscripts for publication. Collaboration is common, as you'll work closely with principal investigators, research assistants, and sometimes external partners. Attention to detail and strict adherence to ethical standards are important in ensuring reliable and valid study outcomes.

What are the key skills and qualifications needed to thrive in the research study position?

To succeed in a Research Study position, you typically need strong analytical skills, attention to detail, and a background in scientific or social science research methodology—usually supported by a relevant degree. Familiarity with data analysis software like SPSS, R, or Python, as well as experience with survey tools and ethics certifications (such as CITI training), is frequently required. Excellent written and verbal communication, organization, and collaboration skills set top candidates apart. These competencies are crucial for accurately collecting, analyzing, and presenting data while working effectively within multidisciplinary research teams.

What kind of careers are in research study?

Careers in research study include roles such as research coordinators, data analysts, research assistants, and principal investigators. These positions often require skills in data collection, analysis, and reporting, and may involve working in clinical, academic, or industry settings with adherence to ethical standards and regulatory guidelines.

What are popular job titles related to Research Study jobs in Dallas, TX?

For Research Study jobs in Dallas, TX, the most frequently searched job titles are:

What job categories do people searching Research Study jobs in Dallas, TX look for?

The top searched job categories for Research Study jobs in Dallas, TX are:

Research Study jobs near you
Infographic showing various Research Study job openings in Dallas, TX as of August 2026, with employment types broken down into 1% As Needed, 87% Full Time, 10% Part Time, and 2% Contract. Highlights an 80% Physical, 4% Hybrid, and 16% Remote job distribution.

Clinical Research Coordinator II

Dallas, TX

DALLAS VA RESEARCH CORPORATION
Scientific Research and Development Services • 1 - 10 employees
Learn more about DALLAS VA RESEARCH CORPORATIONexternal

$24 - $32/hr

Full-time, Part-time

Re-posted 5 days ago

Job description

Summary:  Clinical Research Coordinator 2 is a Part Time or Full Time Non-Exempt Position 

Education and Experience Requirements: 

  • Must be eligible to work in the U.S. and be a U.S. citizen
  • More than 4 years of research experience; or
  • 3+ years of research experience and a Bachelor Degree in a relevant area; or
  • 3+ years of research experience and an LVN; or
  • Greater than 1 year of research experience and a Masters Degree or Ph.D. in a relevant area
  • Nuclear Medicine and/or Oncology experience

SoCRA or ACRP Certification:  Highly desirable and counts as one year of experience

Software Requirements:  Experience with Microsoft Office and research database products

Responsibilities:  The position of Coordinator 2 (“CRC2”) works under light supervision of the Principal Investigator or more experienced coordinator. The Coordinator 2 is responsible for conducting procedures for one or more research studies. The CRC2 may supervise less-experienced Coordinators or Research Assistants. They will maintain the protection of human subjects while meeting the research goals of each project. A Coordinator 2 will consistently exhibit behavior and communication skills that demonstrate DVARC’s commitment to superior customer service and dedication to the care of our veterans.

Supervisors: VANTHCS Principal Investigator, DVARC Director HR and Operations, works closely with Team Leader

Duties:  In addition to the knowledge of the duties of an Assistant Coordinator and a Research Coordinator 1, a CRC2 may have the following duties:

  1. Assists in the design of research survey forms to capture required participant information
  2. Interviews study participants and/or family members to gather research information
  1. Reviews exclusion/inclusion criteria with the Principal Investigator or Senior Coordinator to ensure subject eligibility
  1. Conducts interviews to confirm study eligibility and willingness to follow and complete study procedures and visits
  2. May perform consent process with patients, ensuring inclusion and exclusion criteria are met, taking responsibility for all aspects of research completeness, enrollment notes, administrative duties and data entry
  3. Develops, coordinates and reviews research study procedures to ensure receipt, completeness and accuracy of study data
  4. Coordinates, with the assistance of higher grade staff, all regulatory requirements such as preparing safety reports, adverse event paperwork, FDA compliance, sponsor monitoring and logs, laboratory standards, and maintenance of databases related to regulatory requirements
  5. May assist with the study budget and negotiation of participant payments
  6. Monitors budget, prepares reimbursement requests, approves expenditures and reconciles study accounts
  7. Prepares and submits information in the Case Report Form and submits a billing matrix for funding source and submits to DVARC
  8. Prepares statistical reports, charts and graphs as required
  9. Assists in preparation of annual reports for federal, state, and local agencies
  10. Informs IRB of amendments to research studies
  11. Coordinates collection and data management of national research studies from multiple projects by interacting with internal and external research data managers, patients, and physicians for coordination of tissue samples, lab data and protocols, and other statistical information concerning research study subjects
  12. Serves as primary liaison and prepares annual reports for federal, state, and/or local agencies.
  13. Informs Institutional Review Board of amendments to research studies, and prepares protocols and detailed summaries in lay terms of any new research study
  14. May provide full supervision to personnel of lower grades
  15. May perform lower risk, less complicated procedures in studies, if directed by Principal Investigator
  16. Must be able to do a study start up with the appropriate IRB and R&DC and safety committee.