Clinical Studies Coordinator Clinical Cancer Prevention - Research
- Requisition #: 171356
- Department: Clinical Cancer Prevtn - Rsch
- Location: Houston, TX
- Posted Date: 10/30/2024
The primary purpose of the Coordinator, Clinical Studies is to provide administrative and patient care for the coordination of clinical trials.
JOB SPECIFIC COMPETENCIES:
Research Subject Management
• Coordinates, evaluates and follows patient participation in clinical trials.
• Assists in the collection and evaluation of data from patients during in-person meeting, telephone interviews, and surveys.
• Submits information on adverse events to IRB and sponsors as required.
Data Management
• Tracks protocol related labs, responses and research tests.
• Compiles protocol data for manuscript submission. Enters data into case report forms or designated study databases.
• Coordinates submissions and supervises clinical trial audits. In-house monitoring and reviews of participant charts
• Under supervision of the medical staff and research nurse staff, performs protocol-specific tasks including screening, consenting, ordering tests, collecting specimens and study documentation of patient reported responses.
Trial Conduct Coordination
• Provide study related coordination including writing, submission and maintenance of protocols.
• Develops and maintains a processing and tracking system for all protocol related paperwork.
• Assist with development and writing of grant proposals and maintains contact with funding agencies.
• Develops project timelines for the study team and collaborators
• Trains other support staff in study coordination.
• Communicates with collaborators regarding protocol status and data collection
• Effectively conducts assigned operations of research protocols.
Other duties as assigned
EDUCATION:
Required: Bachelor's degree.
Preferred: Master'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.
Preferred: Ideal candidate will have 2-3 years of population based or clinical trial research experience; RedCap Database experience. Bilingual in English/Spanish 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
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JOB SPECIFIC COMPETENCIES:
Research Subject Management
• Coordinates, evaluates and follows patient participation in clinical trials.
• Assists in the collection and evaluation of data from patients during in-person meeting, telephone interviews, and surveys.
• Submits information on adverse events to IRB and sponsors as required.
Data Management
• Tracks protocol related labs, responses and research tests.
• Compiles protocol data for manuscript submission. Enters data into case report forms or designated study databases.
• Coordinates submissions and supervises clinical trial audits. In-house monitoring and reviews of participant charts
• Under supervision of the medical staff and research nurse staff, performs protocol-specific tasks including screening, consenting, ordering tests, collecting specimens and study documentation of patient reported responses.
Trial Conduct Coordination
• Provide study related coordination including writing, submission and maintenance of protocols.
• Develops and maintains a processing and tracking system for all protocol related paperwork.
• Assist with development and writing of grant proposals and maintains contact with funding agencies.
• Develops project timelines for the study team and collaborators
• Trains other support staff in study coordination.
• Communicates with collaborators regarding protocol status and data collection
• Effectively conducts assigned operations of research protocols.
Other duties as assigned
EDUCATION:
Required: Bachelor's degree.
Preferred: Master'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.
Preferred: Ideal candidate will have 2-3 years of population based or clinical trial research experience; RedCap Database experience. Bilingual in English/Spanish 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: 171356
- 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: No
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