MD Anderson Cancer Center Coordinator, Research Data in Houston, Texas
Coordination of Research Data
Data Collection and Management:
Obtain patient information including demographic, toxicities, and pertinent reports from the Electronic Medical Record (EMR) to extract data points.
Perform data entry and transfer patient information into protocol specific database, case report forms, electronic database (i.e. PDMS, CORe, RedCap and Sponsor Database)
Assist with design of protocol specific database
Retrieve protocol information via PDOL, CORe, Epic and other available sources.
Perform data review, data collection for retrospective studies
Maintain high quality of database and ensure data entry is accurate and timely.
Collaborate with the research team and principal investigators in managing research protocols, assuring protocol compliance, collecting protocol-specific information utilizing a paper and/or computer database system and communicating with patients and staff regarding protocol information (survival, follow-ups, and obtaining records from outside institutions).
Assist with submitting requests for internal pathology specimens for translational research and central pathology review.
Assist with preparation of required regulatory documents for audits by any pharmaceutical/ academic sponsor, FDA, NCI, and/or cooperative groups.
Clinical Research Activities:
Assume responsibilities for minimal risk studies including patient screening, registration, and data collection and retrospective studies
Assist with descriptive data analysis
Assist with abstract/manuscript preparation
Coordinate and send outgoing material and correspondence to institutional, state, and/or federal agencies.
Take responsibility to make sure that IBC research protocols and projects are in compliance with institutional regulations and other governing agencies.
Perform data monitoring for multi-center studies
Attend research meetings and maintains contact with other institutions participating in studies.
Attend classes and/or trainings relevant to performing job.
Attend institutionally and departmentally required training.
Assist department research management team with educating faculty and staff on new regulations.
Prepare reports for committees and meetings to communicate the status of all protocols in relation to regulatory compliance.
Other Other duties as assigned.
Education Required: High school diploma or equivalent.
Education Preferred: Bachelor's degree
Experience Required: Two 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
Requisition ID: 130075
Employment Status: Full-Time
Employee Status: Regular
FLSA: non-exempt, eligible for overtime, and is subject to the provisions of the Fair Labor Standards Act (FLSA)
Work Week: Days
Fund Type: Soft
Pivotal Position: No
Minimum Salary: US Dollar (USD) 33,200
Midpoint Salary: US Dollar (USD) 41,500
Maximum Salary : US Dollar (USD) 49,800
Science Jobs: Yes