This clinical research coordinator (CRC) position may provide study coordination for multiple clinical research studies depending on complexity that range from moderate to complex. This position should be able to perform tasks and make decisions independently, consistently, and accurately, and demonstrate that they have achieved a moderate level of expertise in all their skills and abilities resulting in high quality work
Characteristic Duties and Responsibilities:
Independent knowledge, skills, and abilities within all 8 competency domains is expected:
Scientific Concepts and Research Design
Ethical Participant Safety Considerations
Investigational Products Development and Regulation
Clinical Study Operations (GCPs)
Study and Site Management
Data Management and Informatics
Leadership and Professionalism
Communication and Teamwork
Key duties include:
Working as part of a team to develop and implement clinical research protocols preparing proposals for IRB approval and communication with the IRB on amendments and compliance reporting
Screening patients for enrollment studies
Obtaining consent for inclusion in research studies
Communicating with families enrolled in studies to maintain engagement
Conducting study activities, which may include conducting surveys/interviews and facilitating biologic sample collection
Ensuring integrity of data and biological specimen collection, preliminary processing, and documentation
Gathering and input of information from the electronic medical record (EPIC/MiChart) and research databases (e.g. RedCAP)
Managing database queries and resolving gaps in data collection
Resolving simple questions that come up during research protocols