Coordinator, Clinical Studies - Lymphoma-Myeloma
- Requisition #: 172421
- Department: Lymphoma - Myeloma
- Location: Houston, TX
- Posted Date: 1/3/2025
Clinical Studies Coordinator
MISSION STATEMENT
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.
SUMMARY
JOB SPECIFIC COMPETENCIES
Protocols
Provides all study-related coordination, including writing, submission, and maintenance of protocols. Develops and maintains a processing and tracking system for all protocol-related paperwork. Develops patient care methodology for protocols, including criteria for patient participation. Collects and develops criteria information for protocol submission.
Coordinates, evaluate, and follows patient participation in clinical trials
Reviews patient eligibility of potential study cases and assists in obtaining consent. Follows patients on studies and maintains knowledge of adverse events. Submits information on adverse events to IRB and revises consents. Tracks protocol-related labs, responses, and research tests. Compiles protocol data for manuscript submission. Enters data into case report forms. Maintains necessary data for audits. Schedules patient tests and keeps patients. Supervisor informed about test results and studies.
Sample collection, toxicity reporting, and quality assurance assist in the management of research samples or data as needed. This includes working with many different departments-effectively communicating with these departments to collect data and prevent protocol deviations or violations. Assist in departmental duties and Quality Assurance Rotation.
Regulatory & Administrative:
Collaborates with physicians, mid-level practitioners, research nurses, and data managers to document patient care. Trains other support staff in study coordination. Effectively conducts assigned operations of research protocols.
Inventory Control & Data Management
Coordinates, evaluates and follows patient participation in clinical trials. Assists in the collection and evaluation of data. Under the supervision of the medical and research nurse staff, performs protocol-specific tasks, including screening, ordering tests, collecting specimens, and studying documentation of patient-reported responses.
Education Required - Bachelor's degree.
Experience Required - Three years experience in area of research study or direct patient care obtained from nursing, data gathering or other related experience. May substitute required education degree with additional years of equivalent experience on a one to one basis. With preferred degree, one year of required experience.
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-Remote
MISSION STATEMENT
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.
SUMMARY
JOB SPECIFIC COMPETENCIES
Protocols
Provides all study-related coordination, including writing, submission, and maintenance of protocols. Develops and maintains a processing and tracking system for all protocol-related paperwork. Develops patient care methodology for protocols, including criteria for patient participation. Collects and develops criteria information for protocol submission.
Coordinates, evaluate, and follows patient participation in clinical trials
Reviews patient eligibility of potential study cases and assists in obtaining consent. Follows patients on studies and maintains knowledge of adverse events. Submits information on adverse events to IRB and revises consents. Tracks protocol-related labs, responses, and research tests. Compiles protocol data for manuscript submission. Enters data into case report forms. Maintains necessary data for audits. Schedules patient tests and keeps patients. Supervisor informed about test results and studies.
Sample collection, toxicity reporting, and quality assurance assist in the management of research samples or data as needed. This includes working with many different departments-effectively communicating with these departments to collect data and prevent protocol deviations or violations. Assist in departmental duties and Quality Assurance Rotation.
Regulatory & Administrative:
Collaborates with physicians, mid-level practitioners, research nurses, and data managers to document patient care. Trains other support staff in study coordination. Effectively conducts assigned operations of research protocols.
Inventory Control & Data Management
Coordinates, evaluates and follows patient participation in clinical trials. Assists in the collection and evaluation of data. Under the supervision of the medical and research nurse staff, performs protocol-specific tasks, including screening, ordering tests, collecting specimens, and studying documentation of patient-reported responses.
Education Required - Bachelor's degree.
Experience Required - Three years experience in area of research study or direct patient care obtained from nursing, data gathering or other related experience. May substitute required education degree with additional years of equivalent experience on a one to one basis. With preferred degree, one year of required experience.
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: 172421
- Employment Status: Full-Time
- Employee Status: Regular
- Work Week: Days
- Minimum Salary: US Dollar (USD) 55,500
- Midpoint Salary: US Dollar (USD) 69,500
- Maximum Salary : US Dollar (USD) 83,500
- FLSA: non-exempt and eligible for overtime pay
- Fund Type: Soft
- Work Location: Remote (within Texas only)
- Pivotal Position: No
- Referral Bonus Available?: No
- Relocation Assistance Available?: No
- Science Jobs: Yes
#LI-Remote
