The primary purpose of the Senior Coordinator, Research Data position is to coordinate the implementation of data collection for various studies focusing on cancer prevention, reducing cancer risks and population/survey research.
The Senior Coordinator, Research Data assists with the day-to-day operations including subject recruitment, identifying and monitoring the completion of project-related tasks, maintaining study-related procedures, ensuring protocol and regulatory compliance, and data management oversight.
Coordinate project activities and perform tasks including but not limited to recruiting and consenting study participants, obtaining medical release if necessary, data collection services (in person, by mail or telephone interviews), data entry, and execute study procedures according to protocol. Assure completion of all components of study, such as telephone calls, patient visits, patient interviews, and preparing study mail-out packets. Ensure appropriate completion of questionnaires throughout the course of the study and maintain necessary documentation associated with participation in the study. Ensure all data entered appropriately. Coordinate study procedures for study assessments. Schedule baseline and follow up assessments with participants. Maintain certifications and trainings needed to assist with assessments..
Materials and Procedures Contribute to the development of study related materials (such as consenting scripts, survey questionnaires, and mail-out packets). Draft standard operating procedures for recruitment, collecting data, and train other staff members as needed..
Administrative Research Tasks Provide project updates and reports directly to the PI, Co-PIs, and supervisor as requested. Gather and organize records. Maintain study regulatory binders where appropriate. with planning, organizing, reviewing, and submitting research protocols. Perform literature searches as necessary.
Travel Travel to alternate work locations may be required.

EDUCATION:

Required: High school diploma or equivalent.
Preferred: Bachelor’s degree.

EXPERIENCE:

Required: Four years of related experience. With preferred degree, no experience required.
Preferred: Prefer research or healthcare experience, experience interacting directly with patients. Bilingual in English & Spanish (writing, reading & speaking) is a plus.
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

Additional Information

• Requisition ID: 163365
• Employment Status: Full-Time
• Employee Status: Regular
• Work Week: Days
• Minimum Salary: US Dollar (USD) 41,500
• Midpoint Salary: US Dollar (USD) 52,000
• Maximum Salary : US Dollar (USD) 62,500
• FLSA: non-exempt and eligible for overtime pay
• Fund Type: Soft
• Work Location: Onsite
• Pivotal Position: No
• Referral Bonus Available?: No
• Relocation Assistance Available?: No
• Science Jobs: No

LI-Onsit

Please refer the Job description for details