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This position independently coordinates and is accountable for the overall administration of one or more clinical studies, typically requiring advanced-level knowledge and skills. This position is responsible for coordination of a variety of research projects from pre-study implementation through study closure and will work independently in the acquisition of specimens; extraction and entry of patient data; maintenance of complete and accurate subject data and regulatory documentation; and analysis of data per protocol. This position provides administrative / regulatory support (recruiting, interviewing and scheduling study participants, processing IRB and other regulatory documents) to specific clinical departments in accordance with all federal, state, regulatory agency, and specific institutional requirements. This position provides mentorship and training to lower-level clinical research staff and/or support personnel; works on departmental projects; and contributes to change implementation in the department.
Education
Bachelors degree in related field. (Required)
Masters degree in related field. (Preferred)
Experience
Three years of clinical trial coordination experience (Required)
Certifications
ACRP or SOCRA Clinical Research Certification (Required)
Clinical Research Training Certification. (Preferred)
Phlebotomy Certification (Preferred)
Special Skills
Proven ability to successfully coordinate multiple studies of varying complexity adhering to regulatory and institutional guidelines. (Required)
Proven ability to coordinate studies in multiple departments and/or disciplines and/or disease processes. (Required)
Proven ability to take initiative, be proactive, and use independent judgment to improve research at PC. (Required)
Proven ability to communicate effectively within an interdisciplinary team to ensure safe, efficient, quality patient care. (Required)