Senior Coordinator, Clinical Studies - Orthopaedic Oncology
Job Description
Full job description
The mission of The University of Texas MD 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
The primary purpose of the Clinical Research Program Coordinator position is to provide administrative and patient care services for the coordination of clinical research studies within the Department of Orthopaedic Oncology for the Learning Cancer Outcomes Research Program and the Pelvic Sarcoma Center of Excellence. Serve as the point person for all research related activities for these programs.
JOB SPECIFIC COMPETENCIES
Protocol Management
Data Management
Protocol Development
Other duties as assigned
Education
Required: Bachelor's degree.
Experience
Required: Five years experience in area of research study or direct patient care obtained from nursing, data gathering or related field. May substitute required education degree with additional years of equivalent experience on a one to one basis. With preferred degree, three years 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
SUMMARY
The primary purpose of the Clinical Research Program Coordinator position is to provide administrative and patient care services for the coordination of clinical research studies within the Department of Orthopaedic Oncology for the Learning Cancer Outcomes Research Program and the Pelvic Sarcoma Center of Excellence. Serve as the point person for all research related activities for these programs.
JOB SPECIFIC COMPETENCIES
Protocol Management
- Manage the operation of multiple protocols in collaboration with the principal investigators and study sponsors for LCORP and the Pelvic Sarcoma COE.
- Provides overall coordination and facilitation of clinical research activity and protocol patient care, including patient accrual and screening, obtaining informed consent, patient registration in institutional database, patient follow-up and monitoring, documentation, data collection and analysis, and submission to study sponsors.
- Ensure all research activities are in compliance with institutional policies.
Data Management
- Maintain project databases and ensure accuracy and completion
Protocol Development
- In collaboration with the principal investigator and/or study sponsor, write, process, submit, and maintain all research protocols. Involved with protocol design and cost analysis.
Other duties as assigned
Education
Required: Bachelor's degree.
Experience
Required: Five years experience in area of research study or direct patient care obtained from nursing, data gathering or related field. May substitute required education degree with additional years of equivalent experience on a one to one basis. With preferred degree, three years 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: 166880
- Employment Status: Full-Time
- Employee Status: Regular
- Work Week: Day/Evening, Days
- Minimum Salary: US Dollar (USD) 65,000
- Midpoint Salary: US Dollar (USD) 81,000
- Maximum Salary : US Dollar (USD) 97,000
- 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
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