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Duties and Responsibilities:
• Adheres to Research SOPs
• Adhere to Good Clinical Practices and the study protocols
• Coordinates all research activities of the patient, providing assistance, direction, and information as necessary
• Complete and maintain case report forms per FDA guidelines, and review them against the patient’s medical record for completeness, accuracy, and legibility
• Works closely with physicians, nurses, and other health care professionals to identify patients for clinical trials. Assists with the recruitment and screening of participants according to protocol requirements
• Ensures the accurate transcription of trial data
• Provides education to patients, families and clinic staff regarding research protocol and investigational agents
• Responsible for the comprehensive management of clinical trials conducted at Piedmont Cancer Institute, including entering all orders in EMR for all research specific visits and procedures
• Meet with patient for each visit and maintain accessibility to discuss any questions/concerns regarding study participation
• Dispense study medication in a professional and accountable manner following protocol guidelines, patient diaries, where applicable
• Collect, process and ship blood/urine specimens at scheduled patient visits
• Perform ECGs and administer questionnaires
• Ensure that serious and non-serious adverse events are properly documented and reported per protocol/institutional guidelines
• Submit patient reimbursement requests to Clinical Research Manager
• Attend Investigator Meetings and Protocol Specific Training Webinars/Meetings
• Other duties as assigned
Fill out the form below to get in touch with our business development team, or call us at (781) 328-1132.
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