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Clinical Research Coordinator 2 Jobs
Company | University of Miami |
Address | Miami, FL, United States |
Employment type | FULL_TIME |
Salary | |
Category | Higher Education |
Expires | 2023-09-05 |
Posted at | 9 months ago |
Current Employees:
- Follows the appropriate fundamental requirements of all international, national, and local regulatory bodies.
- Collects, processes, packs, and ships specimens according to protocol, applicable standards and regulations.
- Assist principal investigators, project managers in coordinating Federal and/or industry-sponsored research studies.
- Assists in administrative tasks of study personnel including orientation, documenting core competencies, certification mandates, safety/responsible conduct of research education, and performance reviews.
- Adheres to cultural competency guidelines; implements strategies to meet study participants’ needs for language translation, health literacy, etc.
- Assists with study orientation and protocol related in-services to research team and clinical staff.
- Monitors protocol implementation and study progress; keeps investigators fully apprised of study progress; submits progress reports according to established schedule.
- Distributes study drug materials according to practice standards and clinical credentials as delegated by the Principal Investigator.
- Adheres to University and unit-level policies and procedures and safeguards University assets.
- Assists in participant recruitment and retention activities, and assists in screening potential study participants for eligibility.
- Monitors, documents, reports, and follows-up on study unanticipated/adverse events and protocol deviations.
- Maintains study binders and filings according to protocol requirements, UM and department policy.
- Assists in implementing protocol amendments under direct supervision of the Principal Investigator.
- Performs study procedures, routine tests, data collection/recording, and daily operations of moderate risk clinical research protocols.
- Learns the research team and assists with communications/interactions with sponsor, data coordinating centers, compliance monitors, collaborators, investigators’ academic administrative personnel, and departments.
- Maintains requisite skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies.
- Bachelor’s degree in relevant field required.
- Commitment to the University’s core values.
- Ability to work evenings, nights, and weekends as necessary.
- Ability to work independently and/or in a collaborative environment.
- Bilingual English and Spanish preferred.
- Ability to process and handle confidential information with discretion.
- Minimum 2 years of relevant experience.
- Skill in completing assignments accurately and with attention to detail.
- Ability to analyze, organize and prioritize work under pressure while meeting deadlines.
- Ability to work with children and their caregivers.
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