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Clinical Research Contract Manager

Job

DHR Health Institute for Research and Development

Edinburg, TX (In Person)

$86,000 Salary, Full-Time

Posted 02/24/2026 (Updated 2 days ago) • Actively hiring

Expires 6/21/2026

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Job Description

$57k Per Year DOE (Depends on Experience) Position range in Hidalgo County $62k - $115k Per Year Clinical Research Contract Manager DHR Health Institute for Research and Development
Occupation:
Clinical Research Coordinators
Location:
Edinburg, TX - 78539 Positions available: 1 Job #: 16982425
Source:
WorkInTexas
Posted:
02/24/2026
Updated:
02/27/2026
Expires:
03/28/2026
Web Site:
WorkInTexas Onsite /
Remote:
Work onsite all of the time
Job Type:
Regular, Full Time (30 Hours or More), Permanent Employment Job Requirements and Properties Help for Job Requirements and Properties. Work Onsite Full Time Education Bachelor's Degree Experience 24 Month(s) Schedule Full Time Job Type Regular Duration Permanent Employment Public Transit Available Help for .
Clinical Research Contract Manager:
DHR Health Institute for Research & Development; Edinburg, TX 78539. Coordinate and monitor sponsored research accounts in accordance with study protocols and institutional guidelines. Ensure adherence to clinical trial billing practices and regulatory requirements, including federal, state, sponsor-specific, and institutional policies. Communicate sponsor guidelines, study protocols, and regulatory expectations to the research sta, and administrators to ensure proper conduct according to the contract language and budget. Track and evaluate expenditures and budget activity related to sponsored clinical research to ensure alignment with study budgets, funding agency requirements, and applicable regulations. Prepare and submit interim and final financial reports, in coordination with Research Institute administrators and sponsors, ensuring accuracy and timeliness. Promote effective research management practice by providing guidance and training to the team. Perform additional administrative and coordination duties related to the planning, implementation, and compliance of clinical research projects, as assigned.
Requirements/Special Skills:
Bachelors degree in Healthcare Management or Healthcare Administration and 24 months of employment experience as Compliance Manager. 24 months as a Compliance Manager must include knowledge of local and state laws, legal codes, precedents, government regulations, executive orders, and agency rules. Knowledge of regulatory compliance applicable to biomedical and clinical research. This includes the U.S. Food and Drug Administration (FDA) regulations governing clinical trials, informed consent, and investigational products. Must possess knowledge of regulatory compliance of Institutional Review Board (IRB) regulations and human subject protection. Demonstrable ability in Good Clinical Practice guidelines and compliance, conflict-of-interest disclosures, and research integrity standards

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