×
Register Here to Apply for Jobs or Post Jobs. X

Research Coordinator III - Neurosurgery (Neuro Oncology

Job in Houston, Harris County, Texas, 77246, USA
Listing for: UTHealth Houston
Full Time position
Listed on 2026-08-22
Job specializations:
  • Science
    Clinical Research
Salary/Wage Range or Industry Benchmark: 65000 - 85000 USD Yearly USD 65000.00 85000.00 YEAR
Job Description & How to Apply Below
Position: Research Coordinator III - Neurosurgery (Neuro Oncology)

This position is with the Department of Neurosurgery working with the Neuro-Oncology team in the Research Division. The position would lead initiating clinical trials, implementing active trials, contributing to trial finances, and assisting in trial closeouts.

The ideal candidate should have an understanding of brain tumors and experience leading all clinical trials – industry and federal. Working in collaboration with a multidisciplinary team in the Neuro-Oncology team within the Department of Neurosurgery.

Additional duties may include
  • Assist the Program Manager and Faculty in the development, implementation, and closure of all Neuro-Oncology Clinical Trials
  • Assist in the submission of all IRB protocols, maintain protocols, and ensure compliance in all Neuro-Oncology Clinical Trials.
  • Assist the Program Manager in the administrative direction of study personnel.
Position Summary

Under minimal supervision, assists with human subject research project conduct and management, including participant recruitment and data collection, entry, management, and analysis. Assists with research project logistics, maintaining records, preparing reports, and meeting research milestones and deadlines.

Position Key Accountabilities
  • Assists with human subjects research activities, including participant recruitment, informed consent, data collection through surveys, interviews, and observations, and ensuring that all activities are conducted according to study protocols.
  • Maintains confidential records of collected data, ensures accuracy, compliance and integrity of data. Supports Data Management Sharing (DMS) plan.
  • Finalizes annual progress reports and applications for various committees and ensures that all staff have received the proper training/attended the appropriate training courses.
  • Assists in the preparation of progress and annual reports, contracts and grant proposals to various funding agencies; works closely with the Office of Sponsored Projects on the submission of grants.
  • May assist with regulatory submissions (i.e. Institutional Review Board(s), FDA, etc).
  • Assists investigator with quantitative and qualitative data analysis, including statistical tests and the creation of figures, tables, and graphs. Helps prepare research papers, presentations, and reports including manuscripts for publications and conferences.
  • Prepares or assists in the preparation of budgets, initiates re-budgeting requests based on the needs of research staff, and authorizes expenditures for multiple projects. Attends research planning meetings to prepare budget drafts for departmental leadership approval. Reconciles and monitors invoices.
  • Responsible for coordinating and responding to site monitoring visits, audits, and inspections.
  • May be responsible for maintaining study materials (i.e. test kits, investigational drugs and devices).
  • May provide administrative direction training and guidance to study personnel within department.
  • May provide recommendations by identifying opportunities to enhance, re-terminate, or re-direct resources across various research projects to ensure timely completion of project guidelines.
  • Supports complex scheduling and logistical needs to meet projects' expectations.
  • Performs other duties as assigned.
Certification/Skills
  • Completion of Human Research Subjects training.
  • Demonstrated data management skills.
  • Excellent communication skills both written and verbal.
  • Detail oriented.
  • Work may involve handling biohazardous, chemical, and radiological materials, as well as operating associated equipment. Required safety training and appropriate engineering and administrative controls including the use of personal protective equipment must be followed.
  • Health Services Certified Clinical Research Professional (CCRP) by Society of Clinical Research Associates (SOCRA) preferred.
Minimum Education

​Bachelor's Degree in a related field required;
Master's Degree preferred. May substitute required education with equivalent years of experience beyond the minimum experience requirement.

Minimum Experience

5 Years of relevant experience required. May substitute required experience with equivalent years of education beyond the minimum education…

To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary