Key Responsibilities** **_40% Research Coordinator Duties_** + Research Study Management: + Coordinate the operations of clinical, biomedical, and/or behavioral research studies involving human subjects + Coordinate specialized tasks with the research team such as the operation of equipment, processing of laboratory specimens, administering of treatment and/or medication in accordance with research protocol, assessment of patient reaction to medications and/or treatments as part of a research protocol and identification of potential adverse reactions + Perform certain non-invasive patient-oriented procedures + Responsible for the processing and shipping of study-specific laboratory specimens + Coordinate physician examinations and study protocol for technicians + Assist in planning aspects of team research + Keep study files in compliance with Food and Drug Administration's regulations + Read, interpret and communicate protocol for clinical studies providing data on the safety and efficacy of new drugs + Establish and maintain effective working relationships with patients and their families, professional or community groups and volunteers + Maintain contact with Principal Investigators, Co-Investigators, and public agencies which are involved with aspects of the research + Research Data Management + Maintain records of study data. + **Applicants who do not meet these qualifications WILL NOT be forwarded to the Hiring Manager.** **Additional Qualifications** + Experience in research compliance + Sound knowledge of IRB submission procedures, FDA, GCP, and NIH requirements relating to research involving human subjects + Prior working experience with common eCRF systems (e.g., Inform, Medidata, Medrio, etc.) + Knowledge of OnCore CTMS software + Strong computer skills and competency with Microsoft Office software + Strong attention to detail and ability to multi-task, organize and prioritize multiple projects + Experience in clinical trial processes and implementation of research protocols + Demonstrated ability to work independently with minimal supervision + Ability to communicate effectively both verbally and in writing, and to work effectively with colleagues and study sponsor representatives + Applicants selected for this position who have not already completed the training for clinical research involving human subjects will be required to complete it within 90 days of hire **Preferred Qualifications** + Experience or knowledge working in a clinical setting.