Clinical Research Coord II

Mercy is the seventh largest Catholic health care system in the U.S. serving millions of people annually.

This position is responsible for the day-to-day operational issues related to clinical trials. Activities will include, but not be limited to, volunteer recruitment, informed consent, establishment of study-specific procedures, data collection , case report form maintenance, drug/device/supply inventory maintenance, and interaction with physicians, nurses, office staff, the public, and clinical monitors. Performs related duties as assigned.

* Completes pre-study checklist responsibilities in a timely fashion and with appropriate quality. * Uses screening and promotional practices appropriate for specific studies to effectively enroll patients. * Adheres to all regulatory requirements of clinical research. * Demonstrates a strong working knowledge of assigned protocols and associated processes. * Effectively manages patient visits in terms of preparedness and efficiency for patients, physicians, and SJMRG staff. * Demonstrates preparedness and efficiency when working with study monitors. * Demonstrates appropriate patient monitoring skills, including interviews and diagnostic evaluations. * Attends investigator meetings when appropriate, which will involve travel and time away from work and home. * Utilizes knowledge of pathophysiology and drug properties to monitor for therapeutic efficacy and safety in all patients. * Schedules study volunteers for clinic visits in accordance with protocol requirements and clinic staffing and space needs. * Educates patients about drug use and disease state management, including self-monitoring, dietary considerations, warning signs, etc. * Updates case report forms and source documents in a timely and accurate manner. * Maintains appropriate supplies for clinical trials and maintains accurate inventory records. * Participates in internal quality control monitoring of protocol compliance, patient satisfaction, and recruitment efforts when needed. * Accurately collects and prepares tissue/fluid specimens for laboratory analysis. * Receives and routes telephone calls when needed. * Contributes to an orderly and functional office environment. * Meets Health System attendance standards. GENERAL DUTIES: * Participates in additional activities as needed. * Wears clothing and Health System badge consistent with dress code, and attends to personal hygiene to maintain a clean, well-groomed appearance. * Observes universal precautions consistently. * Wears proper personal protective equipment when appropriate.

Qualifications: Experience: Working knowledge of the research process and clinical trials. Strong familiarity with medical and pharmaceutical terminology, and patient medical records. History of meticulous attention to detail in all aspects of work. Demonstrated history of self-motivation in the workplace. History of excellent work attendance, dependability, and daily performance. Demonstrated willingness to acquire new skills and adapt to changes in workload. Other: Ability to perform basic patient assessments, e.g. vital signs, spirometry, ECGs, phlebotomy, blood glucose monitoring, or willingness to learn. Exceptional communication skills, particularly in face-to-face encounters with healthcare professionals and the public. Ability to interact with health professionals in a respectful and assertive manner. Working knowledge of computer applications, including the Internet and all Microsoft Office components, modems, printers and other computer accessories. Above average proficiency in mathematics, including a working knowledge of the metric system. Ability to work effectively in groups and independently with a high level of efficiency in problem identification and problem solving.