Clinical Research Coordinator 3 (A)
Clinical Research Coordinator 3 (A)
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Job Description
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The Department of Surgery has an exciting opportunity for a Clinical Research Coordinator 3 (A) position. The incumbent serves as an experienced clinical research professional responsible for providing leadership in the planning implementing monitoring and evaluating of multiple clinical research protocols. This role manages multiple studies daily operations carries out study coordination duties from protocol development and initiation to study close-out according to regulatory/sponsor guidelines assures each studys integrity and mentors less experienced Clinical Research Coordinators. The incumbent monitors and maximizes adherence to research standards and regulatory guidelines and approved operational procedures works closely with study team members and other staff/faculty/study sites to ensure study participant safety and adherence to approved protocols manages study-related administrative and human resources tasks facilitates across-the-board flow of information and orchestrates study activities and personnel.
CORE JOB FUNCTIONS
Coordinates the implementation of multiple complex clinical research protocols.
Develops SOPs and templates with guidance from the PI/Clinical Research Manager.
Oversees and facilitates eligibility screening and study recruitment activities; implements strategies to increase accrual.
Manages sample processing packing and shipping according to protocol applicable standards and regulations.
Plans and operationalizes strategies to monitor document report and follow-up on unanticipated occurrences and protocol deviations.
Develops and implements preventive/corrective actions.
Develops disseminates and assures adherence to study-related clinical research best practices/scientific manuals.
Assumes leadership in protocol implementation and study progress keeping investigators apprised of study progress.
Provides leadership in identifying and working through ethical conflicts arising during protocol implementation and refers these conflicts to the Research Ethics Team for consults as needed.
Organizes/manages site visits and internal/external auditing activities as assigned.
Coordinates research team meetings; assures communications across-the-board.
Assures synchronization of study visits/procedures/ clinical tests with data collection schedules established time-points; manages progress of study participants through protocol; expedites overall study progression.
Coordinates the compilation of information needed for research reports; peer-reviewed publications; develops strategies to disseminate information to clinical personnel professional audiences and stakeholders. Follows the appropriate fundamental requirements of all international national and local regulatory bodies.
Maintains requisite skills and mandatory training in safety equality responsible conduct of research continuing education and research competencies.
Adheres to University and unit-level policies and procedures and safeguards University assets.
This list of duties and responsibilities is not intended to be all-inclusive and may be expanded to include other duties or responsibilities as necessary.
CORE QUALIFICATIONS
Bachelors degree in relevant field
CITI certification for the Protection of Human Subjects Research
Minimum 2 years of relevant experience
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The University of Miami offers competitive salaries and a comprehensive benefits package including medical dental tuition remission and more.
UHealth-University of Miami Health System South Floridas only university-based health system provides leading-edge patient care powered by the ground breaking research and medical education at the Miller School of Medicine. As an academic medical center we are proud to serve South Florida Latin America and the Caribbean. Our physicians represent more than 100 specialties and sub-specialties and have more than one million patient encounters each year. Our tradition of excellence has earned worldwide recognition for outstanding teaching research and patient care. Were the challenge youve been looking for.
The University of Miami is an Equal Opportunity Employer - Females/Minorities/Protected Veterans/Individuals with Disabilities are encouraged to apply. Applicants and employees are protected from discrimination based on certain categories protected by Federal law. Click here for additional information.
Job Status:
Full timeEmployee Type:
StaffPay Grade:
A10Required Experience:
IC
Employment Type
Full-Time
