Clinical Research Coordinator enrolling patients in orthopedic studies at Banner Health. Responsible for data collection and patient education within the research protocols.
Responsibilities
This position is responsible for coordinating and/or implementing assigned protocols.
Provides study information and obtains relevant information to and from patients engaged in clinical studies.
Performs tasks required by protocol, which may include obtaining patient medical history, systems review, phlebotomy, EKG, and cognitive assessment on patients.
Triages adverse events and communicates with the research physician regarding the occurrence of adverse events.
Provides educational information to patients and their families.
Ensures uniform implementation of protocols by completing required documentation in a consistent, accurate and timely manner.
Serves as a liaison to other departments and programmatic areas, as well as community agencies.
Ensures that primary referring physicians receive timely progress notes on the patient’s diagnosis and treatment.
May assume primary responsibility in the implementation and management of new clinical trials in a knowledgeable and collaborative manner.
Requirements
Must possess knowledge of clinical research methodologies as normally obtained by the completion of a bachelors' degree in a healthcare field.
Experience typically gained through two to four years clinical research experience.
Familiarity with medical and clinical terminology.
Must have excellent organizational and task management skills.
Ability to maintain confidentiality of patient and study information.
Ability to maintain knowledge of Federal and State regulations governing practice as well as Institute policies and procedures related to medical and nursing practice.
Excellent human relations, organizational and communication skills are required.
Benefits
See the Benefits Guide under the Total Rewards section of this posting , to learn more about our great benefit package!
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