Coordinator, Clinical Studies - Thoracic Head and Neck Medical Oncology - MD Anderson
Houston, TX
About the Job
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. The University of Texas MD Anderson Cancer Center in Houston is one of the world's most respected centers focused on cancer patient care, research, education, and prevention. It was named the nation's No. 1 hospital for cancer care in U.S. News & World Report's 2022-2023 rankings. It is one of the nation's original three comprehensive cancer centers designated by the National Cancer Institute.
Coordination of activities related to initiation and conduct of clinical trials
•Develops and maintains a process and tracking system for all protocol related paperwork. Ensure research charge tickets are used appropriately.
•Communicates verbally and in writing, as needed with internal reviewers or external agencies.
•Coordinates, evaluates and follows patient progress while on studies maintaining knowledge of adverse events, protocol related labs and research tests, protocol responses. Collaborates with the multidisciplinary team as necessary to achieve the objectives of the trial.
•Collaborates with physicians, mid-level practitioners, and research nurses and data managers to assure appropriate documentation of patient care and obtain the necessary information required by the protocol.
• Screen patients for protocol eligibility through personal interviews and/or medical record review in inpatient and outpatient setting. Identify and meet the educational, emotional and psychosocial needs of patient and their families while on clinical trials.
•Coordinate, evaluate, and follow the patient's participation in clinical settings. Collaborate with the multidisciplinary team as necessary to document patient care, achieve objectives of clinical trials and maintain patient safety.
•Performs protocol specific duties under direct supervision of protocol PI, research nurses manager/supervisor.
•Assist in obtaining consent for studies
•Assist in screening for adverse events
•Schedule patient tests; keep patients informed about test results and studies
•Monitor protocol compliance by assisting in coordination of protocol specific lab, radiographic, and clinical evaluation of patients.
Assist in the coordination of data entry on departmental clinical research studies
•Register patients on research protocols by verifying eligibility/exclusion criteria and entering patients in PDMS per protocol. Communicate necessary registration information to sponsoring Drug Company as directed by PI, and with assistance of the research nurse.
•Complete case report forms in a timely and accurate fashion. Retrieve protocol related data as documented in the medical record and accurately enter it into a computerized database or on a handwritten case report form.
•Develop and maintain databases for collection of research studies
•Assist in the preparation of scheduled status reports describing interim data, using CORE
•Make survival call and appropriately record the data
•Generate CORE data reports, protocol summary reports and user generated data reports as requested
•Prepare reports for the sponsoring agency, as specified by reporting requirements (e.g. monthly, semiannually, and annually for NCI studies).
Maintain a high level of professional expertise and credibility through educational programs, including on-site training and off-site conferences •Attend departmental research meetings and conferences.
•Attend approved off-site meetings and conferences.
•Supplement education as needed through use of reference materials, lectures, etc.
•Be punctual in arriving at all professional functions.
•Inform appropriate staff and arrange coverage for necessary functions when absent
•Other duties as assigned.
Other duties as assigned.
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-Hybrid
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. The University of Texas MD Anderson Cancer Center in Houston is one of the world's most respected centers focused on cancer patient care, research, education, and prevention. It was named the nation's No. 1 hospital for cancer care in U.S. News & World Report's 2022-2023 rankings. It is one of the nation's original three comprehensive cancer centers designated by the National Cancer Institute.
Coordination of activities related to initiation and conduct of clinical trials
•Develops and maintains a process and tracking system for all protocol related paperwork. Ensure research charge tickets are used appropriately.
•Communicates verbally and in writing, as needed with internal reviewers or external agencies.
•Coordinates, evaluates and follows patient progress while on studies maintaining knowledge of adverse events, protocol related labs and research tests, protocol responses. Collaborates with the multidisciplinary team as necessary to achieve the objectives of the trial.
•Collaborates with physicians, mid-level practitioners, and research nurses and data managers to assure appropriate documentation of patient care and obtain the necessary information required by the protocol.
• Screen patients for protocol eligibility through personal interviews and/or medical record review in inpatient and outpatient setting. Identify and meet the educational, emotional and psychosocial needs of patient and their families while on clinical trials.
•Coordinate, evaluate, and follow the patient's participation in clinical settings. Collaborate with the multidisciplinary team as necessary to document patient care, achieve objectives of clinical trials and maintain patient safety.
•Performs protocol specific duties under direct supervision of protocol PI, research nurses manager/supervisor.
•Assist in obtaining consent for studies
•Assist in screening for adverse events
•Schedule patient tests; keep patients informed about test results and studies
•Monitor protocol compliance by assisting in coordination of protocol specific lab, radiographic, and clinical evaluation of patients.
Assist in the coordination of data entry on departmental clinical research studies
•Register patients on research protocols by verifying eligibility/exclusion criteria and entering patients in PDMS per protocol. Communicate necessary registration information to sponsoring Drug Company as directed by PI, and with assistance of the research nurse.
•Complete case report forms in a timely and accurate fashion. Retrieve protocol related data as documented in the medical record and accurately enter it into a computerized database or on a handwritten case report form.
•Develop and maintain databases for collection of research studies
•Assist in the preparation of scheduled status reports describing interim data, using CORE
•Make survival call and appropriately record the data
•Generate CORE data reports, protocol summary reports and user generated data reports as requested
•Prepare reports for the sponsoring agency, as specified by reporting requirements (e.g. monthly, semiannually, and annually for NCI studies).
Maintain a high level of professional expertise and credibility through educational programs, including on-site training and off-site conferences •Attend departmental research meetings and conferences.
•Attend approved off-site meetings and conferences.
•Supplement education as needed through use of reference materials, lectures, etc.
•Be punctual in arriving at all professional functions.
•Inform appropriate staff and arrange coverage for necessary functions when absent
•Other duties as assigned.
Other duties as assigned.
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: 170377
- 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: Hybrid Onsite/Remote
- Pivotal Position: No
- Referral Bonus Available?: No
- Relocation Assistance Available?: No
- Science Jobs: Yes
#LI-Hybrid
Source : MD Anderson