Senior Research Data Coordinator - Breast Medical Oncology
- Requisition #: 173090
- Department: BMO Department
- Location: Houston, TX
- Posted Date: 2/5/2025
The mission of The University of Texas M. D. Anderson Cancer Center is to eliminate cancer in Texas, the nation, and the world through outstanding programs that integrate patient care, research and prevention, and through education for undergraduate and graduate students, trainees, professionals, employees and the public.
KEY FUNCTIONS
Coordinates non-therapeutic research studies in accordance with Good Clinical Practice, Federal regulations and institutional policies. Under the supervision of medical staff, assists the investigator in the overall conduct of assigned laboratory trials through the following activities:
Performs protocol-specific duties under the supervision of the protocol Physician Investigator to meet the protocol requirements and compliance including, but not limited to:
Coordinates the acquisition of research blood and tissue samples. Visually monitors, manages, and orders the consumable lab supplies necessary to meet protocol requirements for research specimens. Maintains and manages documentation of research specimens and research supplies.
Communicates and collaborates with other groups within the department and institution such as regulatory, financial team, research team, etc. to successfully manage research study.
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
Additional Information
#LI-Hybrid
KEY FUNCTIONS
Coordinates non-therapeutic research studies in accordance with Good Clinical Practice, Federal regulations and institutional policies. Under the supervision of medical staff, assists the investigator in the overall conduct of assigned laboratory trials through the following activities:
- Actively participates in protocol meetings, such as investigator and initiation meetings.
- Manages non-therapeutic research studies at appropriate intervals and participates in monitoring and audit activities.
- Coordinates, evaluates, and documents patient participation in non-therapeutic research trials.
- Appropriately documents findings in the medical record in collaboration with physicians, mid-level providers, research nurses, and data managers.
- Appropriately keeps patient logs of screening and patients on-study. Will maintain a patient binder for each study with source documents.
Performs protocol-specific duties under the supervision of the protocol Physician Investigator to meet the protocol requirements and compliance including, but not limited to:
- Screening and determination of eligibility of potential new patients.
- Assisting in the informed consent process, under supervision.
- Schedules and tracks protocol-specific tests and procedures.
- Performs basic data entry for assigned research studies focusing on continuous patient follow-up.
- Assist the investigator in data file preparation.
- Participates in data review meetings as required by the department.
Coordinates the acquisition of research blood and tissue samples. Visually monitors, manages, and orders the consumable lab supplies necessary to meet protocol requirements for research specimens. Maintains and manages documentation of research specimens and research supplies.
Communicates and collaborates with other groups within the department and institution such as regulatory, financial team, research team, etc. to successfully manage research study.
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
Additional Information
- Requisition ID: 173090
- 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: Hybrid Onsite/Remote
- Pivotal Position: No
- Referral Bonus Available?: No
- Relocation Assistance Available?: No
- Science Jobs: No
#LI-Hybrid
