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Senior Research Coordinator

Job Description:
Responsibilities Under the direct supervision of the Director of Clinical Research and general supervision of the Vice Chair, Research within the Radiology Office of Research Affairs (ORA), the incumbent is responsible for managing the logistical and administrative aspects of clinical research studies.
The SRAIII will function as a study coordinator across all assigned imaging-research programs, working closely with faculty principal investigators.
The SRAIII will coordinate, manage and conduct clinical research studies in close collaboration with different departments (Modality directors/managers, contracts and grants management) to ensure compliance, safety and ethical conduct of clinical research trials.
Research duties are performed independently under the general supervision of the Director of Clinical Research, others who assign work and assigned project investigators.
Qualifications College degree or 5 years of professional research or analytical experience; or an equivalen combination of education and experiene.
Ability to supervise and train SRAs/Study Coordinators and other staff or personnel involved in the conduct of research studies and clinical trials.
Skill in analyzing information, problems, situations and procedures to define objectives, identify patterns and formulate conclusions.
Skill in setting priorities, which accurately reflect the relative importance of job responsibilities.
Demonstrated ability to organize, initiate and work independently to address responsibilities; must have strong time management skills.
Skills in facilitating meetings with faculty, administrative-level professionals, research staff, etc.
from diverse backgrounds and different service sectors.
Effective interpersonal, oral, and written communication skills; knowledge of medical terminology; ability to effectively and clearly communicate research goals to faculty investigators, research team, support staff, etc.
Demonstrated ability to interact diplomatically and sympathetically with a patient population in varying degrees of health.
Demonstrated strong work ethic and dedication.
Ability to work a flexible schedule in order to meet changing priorities.
Previous experience in university-wide, state, and federal regulatory management in clinical trials.
Knowledge of the preparation of research regulatory documents, informed consents, and IRB submissions.
Ability to work closely and effectively with a variety of project personnel under a high level of stress.
Skill in using computers; working knowledge of word processing, spreadsheet, database and presentation programs.
Skill in organizing and maintaining accurate, up-to-date files and records for audits and other follow-up activities.
Experience in data management of clinical research protocols, including the completion of case report forms and other study documents.
Knowledge in FDA regulations (IND, IDE), ICH guidelines and Good Clinical Practice ACRP or SoCRA ( or equivalent certification ).
Ability to assist in the preparation of research presentations and manuscripts of publishable quality.
California phlebotomy certification preferred.


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