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|Clinical Research Coordinator 3 - Neurology|
Company: University of Miami
Location: Miami, FL
Employment Type: Full Time
Date Posted: 08/09/2022
Expire Date: 10/09/2022
Job Categories: Science, Research & Development
Clinical Research Coordinator 3 - Neurology|
Department Specific Functions:
The ALS Center at the University of Miami seeks an experienced clinical research coordinator to join a team of about 20 talented clinical research professionals focused on the study of amyotrophic lateral sclerosis. Ongoing studies include a mix of investigator-initiated studies, industry sponsored studies, and multi-center studies coordinated by members of the ALS Center. The successful candidate will have significant experience and expertise in clinical research, enjoy working as part of a highly collaborative and synergistic team, have excellent communication skills, and be passionate about producing high quality work that meaningfully advances scientific progress. This position also offers exciting opportunities for professional growth. Please visit our website for more information about the University of Miamiís ALS Center (www.als-miami.org).
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.
Bachelorís degree in relevant field required with a minimum of 4 years of relevant experience required. Any appropriate combination of relevant education, experience and/or certifications may be considered.
Certification and Licensing:
Current Research Coordinator certification by the Association of Clinical Research Professionals or Society of Clinical Research Associates for a minimum of 6 months
Knowledge, Skills and Attitudes:
Skill in collecting, organizing and analyzing data.
Ability to recognize, analyze, and solve a variety of problems.
Ability to analyze, organize and prioritize work under pressure while meeting deadlines.
Ability to process and handle confidential information with discretion.
Ability to work independently and/or in a collaborative environment.