Dallas, TX · On-site
$24 - $32/hr
Maintain Trial Master File (TMF), Investigator Site File (ISF), and essential study documents. * Report adverse events and serious adverse events according to protocol and regulatory requirements.
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Dallas, TX · On-site
$24 - $32/hr
Maintain Trial Master File (TMF), Investigator Site File (ISF), and essential study documents. * Report adverse events and serious adverse events according to protocol and regulatory requirements.
Mansfield, TX · On-site
Experience using CTMS, Electronic Data Capture (EDC), electronic Trial Master File (eTMF), or similar clinical research systems. * ACRP or SOCRA certification (CCRC or CCRP), or a commitment to ...
Mansfield, TX · On-site
Experience using CTMS, Electronic Data Capture (EDC), electronic Trial Master File (eTMF), or similar clinical research systems. * ACRP or SOCRA certification (CCRC or CCRP), or a commitment to ...
$87K - $145K/yr
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...
$87K - $145K/yr
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...
$120K - $135K/yr
Maintainaccurateandtimelymonitoring documentation, including trip reports and trial master file records * Collaborate with vendors, clinical sites, and cross-functional teams to support study ...
$120K - $135K/yr
Maintainaccurateandtimelymonitoring documentation, including trip reports and trial master file records * Collaborate with vendors, clinical sites, and cross-functional teams to support study ...
Plano, TX · On-site
Support regulatory submissions, audits, and inspections by maintaining inspection-ready Trial Master Files (TMF) and related clinical documentation. * Collaborate with Regulatory Affairs to ensure ...
Plano, TX · On-site
Support regulatory submissions, audits, and inspections by maintaining inspection-ready Trial Master Files (TMF) and related clinical documentation. * Collaborate with Regulatory Affairs to ensure ...
Dallas, TX · On-site
$87K - $145K/yr
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...
Dallas, TX · On-site
$87K - $145K/yr
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...
Dallas, TX · On-site
$87K - $145K/yr
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...
Dallas, TX · On-site
$87K - $145K/yr
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...
Houston, TX · On-site
$87K - $145K/yr
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...
Houston, TX · On-site
$87K - $145K/yr
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...
Fort Worth, TX · On-site
$87K - $145K/yr
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...
Fort Worth, TX · On-site
$87K - $145K/yr
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...
Houston, TX · On-site
$87K - $145K/yr
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...
Houston, TX · On-site
$87K - $145K/yr
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...
San Antonio, TX · On-site
$87K - $145K/yr
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...
San Antonio, TX · On-site
$87K - $145K/yr
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...
San Antonio, TX · On-site
$87K - $145K/yr
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...
San Antonio, TX · On-site
$87K - $145K/yr
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...
Houston, TX · On-site
$120K - $135K/yr
Maintain accurate and timely monitoring documentation, including trip reports and trial master file records * Collaborate with vendors, clinical sites, and cross-functional teams to support study ...
Houston, TX · On-site
$120K - $135K/yr
Maintain accurate and timely monitoring documentation, including trip reports and trial master file records * Collaborate with vendors, clinical sites, and cross-functional teams to support study ...
San Antonio, TX · On-site
$87K - $169K/yr
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...
New
San Antonio, TX · On-site
$87K - $169K/yr
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...
New
Austin, TX · On-site
$87K - $169K/yr
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...
New
Austin, TX · On-site
$87K - $169K/yr
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...
New
Shenandoah, TX · On-site
$71K - $189K/yr
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...
Shenandoah, TX · On-site
$71K - $189K/yr
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...
$71K - $189K/yr
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...
$71K - $189K/yr
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...
Austin, TX · On-site
$87K - $169K/yr
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...
New
Austin, TX · On-site
$87K - $169K/yr
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...
New
Abilene, TX · On-site
$71K - $189K/yr
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...
Abilene, TX · On-site
$71K - $189K/yr
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...
Shenandoah, TX · On-site
$71K - $189K/yr
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...
Shenandoah, TX · On-site
$71K - $189K/yr
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP ...
The most popular types of Trial Master File jobs in Texas are:
For Overnight Trial Master File jobs in Texas, the most frequently searched job titles are:
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Cities in Texas with the most Overnight Trial Master File job openings:
Dallas, TX • On-site
$24 - $32/hr
Full-time
Medical, PTO
Re-posted 15 days ago
Job Title : Clinical Research Coordinator (CRC)
Experience : 0–3 Years
Location : Dallas, Texas
Employment Type : Full-time
Job Summary:-
We are looking for a motivated and detail-oriented Clinical Research Coordinator to support the planning, execution, and management of clinical research studies. The ideal candidate should have 0–3 years of experience in clinical research and a strong understanding of Good Clinical Practice (GCP), ICH guidelines, and regulatory requirements. Fresh graduates with relevant internships or clinical research training are encouraged to apply.
Key ResponsibilitiesCoordinate and manage clinical research studies in compliance with study protocols, ICH-GCP guidelines, and applicable regulations.
Screen, recruit, and enroll study participants.
Obtain informed consent from study participants.
Schedule and coordinate patient visits and follow-up appointments.
Collect, verify, and maintain accurate study documentation and source data.
Enter clinical data into Electronic Data Capture (EDC) systems.
Maintain Trial Master File (TMF), Investigator Site File (ISF), and essential study documents.
Report adverse events and serious adverse events according to protocol and regulatory requirements.
Coordinate with investigators, sponsors, CROs, and ethics committees.
Prepare for monitoring visits, audits, and regulatory inspections.
Ensure protocol compliance and participant safety throughout the study.
Assist with study start-up, close-out activities, and regulatory submissions.
Bachelor's or Master's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Microbiology, or a related field.
0–3 years of experience in clinical research or clinical trial coordination.
Knowledge of ICH-GCP, FDA, and local regulatory guidelines.
Familiarity with EDC systems and Microsoft Office.
Strong organizational, communication, and documentation skills.
Ability to work independently and as part of a multidisciplinary team.
GCP Certification.
Clinical Research certification is an added advantage.
Experience with site coordination or patient recruitment.
Knowledge of clinical trial documentation and regulatory submissions.
Clinical Trial Coordination
ICH-GCP Compliance
Patient Recruitment
Informed Consent Process
Source Documentation
Electronic Data Capture (EDC)
Trial Master File (TMF)
Regulatory Documentation
Adverse Event Reporting
Data Management
Communication & Coordination
Attention to Detail
Time Management
Competitive salary
Health insurance
Performance-based incentives
Training and career development opportunities
Paid leave and holidays
Exposure to global clinical research projects
Interested candidates can submit their updated resume along with a cover letter highlighting their clinical research experience, certifications, and relevant skills.
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It services
11 - 50 Employees
Lewes, DE, US
2013
