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Job description
Description The Senior Clinical Research Coordinator contributes to the overall operational management of clinical research/trial/study activities related to research activities in the Department of Urology Center for Pelvic Health and Wellness. The incumbent will support clinical research coordination, regulatory and research compliance including IRB submissions, federal grant administration, data management and research project management. The Senior Clinical Research Coordinator will provide the infrastructure necessary to support the Center's expanding research portfolio by strengthening research operations, maintaining regulatory compliance, and support continued growth of the Center's clinical and translational research program.
Annual salary range: 93,927.51 - 151,099.73
Qualifications Required:
Bachelor's Degree or three-to seven years of study coordination or clinical research coordination experience
Ability to work efficiently and complete tasks with a high degree of accuracy.
Ability to organize multiple projects for efficiency and cost-effectiveness.
Analytical skills sufficient to work and solve problems.
Ability to work flexible hours to accommodate research deadlines.
Ability to concentrate and focus in a work environment that contains distracting stimuli and competing deadlines.
Ability to be flexible in handling work delegated by more than one individual or in the course of delegating work.
Strong interpersonal communication skills to effectively and diplomatically interact with others, including institutional leadership.
Strong written communication skills, ability to compose advanced correspondence and manage large file systems.
Advanced typing and computer skill/ability including word-processing, use of spreadsheets, email and data entry.
Ability to handle confidential material with judgement and discretion.
Skill in managing diverse, complex tasks and information transfer among multiple constituents.
Sufficient math ability and knowledge of clinical trials budgeting processes to manage the preparation of clinical trial budgets.
Advance knowledge of the clinical research regulatory framework and institutional requirements.
Ability to supervise and delegate clerical work as needed.
Advanced knowledge of Good Clinical Practice (GCP) for clinical research.
Strong knowledge of FDA Code of Federal Regulations (CFR) and ICH Good Clinical Practice (GC) for clinical research. .
Be available to work in more than one environment, travel to meetings, off-site visits, conferences, etc
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.