🌎
This job posting isn't available in all website languages

(While navigating through the site, please be sure to disable your pop-up blocker.)


Senior Research Data Coordinator - Health Services Research

📁
Research
💼
Health Services Research 600119
📅
137942 Requisition #
Sign Up for Job Alerts

The primary purpose of the Coordinator, Clinical Studies is to coordinate the production and evaluation of evidence-based decision aids and conduct dissemination and implementation research activities for grant-funded projects in the department of Health Services Research. Responsibilities include writing educational content, testing and modifying content with learner audiences, maintaining source documents, performing patient interviews, and coordinating research.

Job Specific Competencies:

Study coordination:

  • Provides study-related coordination necessary for research projects
  • Contributes to the writing, submission, and maintenance of study protocols
  • Creates and maintains regulatory binder, source documents, and research databases
  • Creates procedure manuals and assists with preparation for IRB audits
  • Schedules and facilitates team meetings
  • Writes meeting minutes and identifies action items
  • Enters and updates all action items into Microsoft Planner
  • Facilitates timely communication among team members and outside collaborators

Study recruitment and data collection:

  • Develops and maintains databases for research data collection
  • Enrolls eligible participants in research studies, determines patient eligibility, and obtains informed consent
  • Collects data for studies (e.g. formative interviews, surveys, cognitive testing and user testing, implementation data)
  • Enters and verifies research data in study databases
  • Conducts and transcribes qualitative interviews

Decision aid production:

  • Coordinates the design and production of decision aids
  • Designs educational modules and programs including scripts, flow diagrams, and storyboards
  • Maintains production and source documents
  • Acts as liaison with the decision aid production team
  • Modifies decision aid components based on user testing

Other duties as assigned. 

EDUCATION:
Required: High school diploma or equivalent.

Preferred: Bachelor's degree.

EXPERIENCE:
Required: Four years of related experience. With preferred degree, no experience required.

It is the policy of The University of Texas MD Anderson Cancer Center to provide equal employment opportunity without regard to race, color, religion, age, national origin, sex, gender, sexual orientation, gender identity/expression, disability, protected veteran status, genetic information, or any other basis protected by institutional policy or by federal, state or local laws unless such distinction is required by law. http://www.mdanderson.org/about-us/legal-and-policy/legal-statements/eeo-affirmative-action.html

My Submissions

Track your opportunities.

My Submissions

Similar Listings

Genomic Med Rsch Department 710562

United States, Texas, Houston, Houston (TX Med Ctr)

📁 Research

Requisition #: 138028

Lymphoma-Myeloma - Research 600664

United States, Texas, Houston, Houston (TX Med Ctr)

📁 Research

Requisition #: 137876

Leukemia 405400

United States, Texas, Houston, Houston (TX Med Ctr)

📁 Research

Requisition #: 136209