Clinical Research Study Coordinator
Clinical Research Study Coordinator
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$ 53609 - 60549
1 Vacancy
Job Description
Reporting to the Scientific Research Manager this position is responsible for supporting the clinical activities on a variety of oncology research studies managed by the Translational Science and Health Services unit in the UNC Lineberger Comprehensive Cancer Center LCCC Clinical Trials Office. These activities include adhering to established timelines and standards organizing meetings facilitating communication between the study team conducting patient screening and informed consents HIPAA and patient followups managing documentation specimen handling data abstraction and data entry. Adhering to GCP guidelines this position ensures study compliance with all regulatory and ethical requirements including IRB standards and manages the documentation necessary to meet these standards. The ideal candidate will have strong analytical organizational and interpersonal skills with a passion for contributing to research that drives meaningful change in healthcare outcomes.
Required Qualifications Competencies And Experience
Possess strong decisionmaking and taskprioritization skills; the ability to problemsolve and troubleshoot issues. High level of accuracy and attention to detail. Ability to thoroughly document procedures. Customeroriented and teamoriented. Demonstrated ability to communicate professionally verbally and in writing. Experience using Microsoft Word Excel & PowerPoint. Knowledge of ICH GCP Federal Regulations and Guidelines. Demonstrated ability to plan work and coordinate multiple projects. Familiarity with software for data management such as REDCap.
Preferred Qualifications Competencies And Experience
Some experience with direct patient contact in the hospital/clinic setting; preferably in a research context. Active CCRP / CCRC certification. Experience or familiarity with medical terminology medical record chart review and data abstraction. Prior experience with translational science projects including standard operating procedures for biospecimen procurement and coordination. Demonstrated ability to operate at a high degree of independence. Demonstrated ability to coordinate studies of high complexity. Experience coordinating research; including obtaining informed consent and enrolling subjects into protocols.
Work Schedule
Monday Friday 8:30AM 5:30PM
Required Experience:
Staff IC
Employment Type
Full-Time
