Clinical Research Coordinator

Position: Clinical Research Coordinator I
* Perform specific protocol procedures such as scheduling study visits and procedures, interviewing subjects, collecting and processing study specimens, taking vital signs, collecting study ECG’s, etc.
* Understands study protocols and ensures all team members adhere to protocol specific procedures for patient safety and data quality assurance. Coordinates, completes and monitors the daily clinical trial activities and performs a variety of duties involved in the collection, compilation, documentation and reporting of clinical research data.
* Works under the general direction of a departmental, clinical research manager and/or the Office of Clinical Research (OCR) in partnership with the Principal Investigator (PI), Co
- Investigator(s) and other study personnel.
* Works with the PI, clinical research manager, department, sponsoring agencies, and the OCR to support and provide guidance on the administration of the compliance, financial, and other related aspects of the clinical study.
* Plays a critical role in ensuring compliance with the study protocol, Federal guidelines, Local guidelines, and in accordance with Good Clinical Practice (GCP).
* Coordinates and may participate in quality assurance reviews conducted by study sponsors, federal agencies, or specially designated review groups.
* Analyzes and completes study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.
* Accountable for all tasks in basic clinical studies.
* Assists with various professional, organizational, and operational tasks under direct supervision.
* Performs other related work as needed.
* Research experience or related experience.
* Knowledge of medical terminology/environment.
* Phlebotomy experience.
* Strong communication skills (verbal and written).
* Excellent interpersonal skills.
* Adaptability to changing working situations and work assignments.
* Ability to comprehend technical documents.
* Ability to develop and manage interpersonal relationships.
* Ability to exercise absolute discretion regarding confidential matters.
* Ability to follow written and/or verbal instructions.
* Ability to handle sensitive matters with tact and discretion.
* Ability to pay attention to detail.
* Ability to perform multiple tasks simultaneously.
* Excellent time management and ability to prioritize work assignments.
* Ability to train or teach others.
* Working knowledge of Good Clinical Practices (GCP).When applying, the document(s)
** MUST
* * be uploaded via the
** My Experience
** page, in the section titled
** Application Documents
** of the application.

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