University of Pennsylvania Clinical Research Coordinator A (Cancer Center) in Philadelphia, Pennsylvania
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Posted Job Title
Clinical Research Coordinator A (Cancer Center)
Job Profile Title
Clinical Research Coordinator A
Job Description Summary
This full time staff member will support the clinical research program at the Basser Center for BRCA. S/he will be responsible for identifying eligible participants and consenting participants to genetics-related research protocols. Recruitment and enrollment will include documentation and tracking of participant enrollment in study databases (REDCap), Basser systems (Progeny and ACCARD), as well as ACC required documentation (CTMS). The research coordinator will be responsible for coordinating both survey data collection in REDCap, and the collection and tracking of biospecimens. He/she will follow participants longitudinally, collecting/abstracting data and samples as required by protocols. Study recruitment will be a combination of clinic-based patient recruitment, as well as remote telephone consent. The research coordinator will assist in other tasks related to the project including coordination of and preparation for study meetings. This individual must be organized and able to prioritize. THIS POSITION IS CONTINGENT UPON FUNDING
This full time staff member will support the clinical research program at the Basser Center for BRCA. S/he will be responsible for enrolling participants to genetics-related research protocols. The research coordinator will be responsible for coordinating the survey data collection, handling participant recruitment and follow up, and basic data entry. In addition, the research coordinator will assist in subject follow-up via phone and mail, clinic-based patient recruitment, and administrative support. The research coordinator will assist in other tasks related to the project including coordination of and preparation for study meetings. This individual must be organized and able to prioritize.
Recruit, screen, and enroll potential study subjects as specified per protocols.
Complete, organize, and maintain all paper and electronic data.
Enter data into database system in a careful and timely manner.
Attend investigator and staff meetings.
Show vigilance in patient protection, protocol compliance, and data quality.
Adhere to all University of Pennsylvania, informed consent form (ICF), and IRB guidelines.
QualificationsBA and 1 - 2 years professional experience, or equivalent combination of education and experience required. Research or hospital administrative experience preferred.
Effective communication and writing skills
Demonstrated ability to work as part of a team as well as independently
Experience with Microsoft Office suite require
Action Oriented; Boss Relationships; Ethics and Values; Integrity and Trust; Interpersonal Savvy; Learning on the Fly; Listening; Organizing; Planning; Priority Setting; Self-Knowledge; Standing Alone; Technical Learning; Time Management
THIS POSITION IS CONTINGENT UPON FUNDING
Job Location - City, State
Department / School
Perelman School of Medicine
$36,401.00 - $55,814.33
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