Research Coordinator

4 weeks ago


San Antonio, United States UT Health San Antonio Full time

Job Summary:

Under general supervision, provides routine technical assistance in performing assigned and delegated tasks in support of clinical research projects with a focus on patient enrollment, data, and biospecimen collection.

Education:

* Bachelor's in a basic or applied clinical science is required with a degree in public health preferred.

Experience:

* Three (3) years of progressive experience in grant administration, research coordination, data collection, and/or facilitating the patient experience in research projects is required. Previous clinical research project experience is preferred.

Job Duties:

1. Screens participants for eligibility, obtains informed consent, completes patient enrollment, and follow up.

2. Collects and processes different types of biospecimens (for example: urine, stool, blood, nasal swabs, etc.).

3. Assists with research projects of limited complexity for clinical and population science.

4. Interviews participants and abstracts data from medical charts into standardized case report forms.

5. Provides routine technical assistance in performing assigned and delegated tasks in support of research projects.

6. Performs assigned clerical and technical duties in a research or clinical lab setting.

7. Performs routine tasks with direction from supervisor, manager, or higher-level technician.

8. Carries out general laboratory inventory and maintenance.

9. Coordinates multiple research protocols and grant submissions.

10. Assists with monitoring budgets, spending, purchasing and participant payments.

11. Creates, completes, and tracks forms and reports for study sponsors.

12. Maintains research subject files for each clinical study and enters all subject data into research database.

13. Monitors ongoing activities on various research studies to ensure compliance with local, state & federal regulations.

14. Performs all other duties as assigned.

Additional Licenses and Certification:

* Certified Clinical Research Professional (CCRP) is preferred.



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