The pharmacist will work with patients through both face-to-face interactions and telephonic patient management. The Hepatitis C Clinical Coordinator collaborates with prescribers, nurses, and other members of the health care team and serves as a preceptor for pharmacy students and residents.
Supports senior research staff by assisting in the day to day operations including data collection and maintenance. Monitors research processes and procedures to ensure data quality is in accordance with corporate standards.
Represents department at research and protocol initiation meetings. Attends and participates in various in-service and external trainings, workshops, conferences and other relevant programs for professional growth and development.
Designs, implements, and evaluates education programs for staff by providing expertise to ensure existing and future education programs, including orientation and ongoing instruction as relevant to individual/group learning needs and patient care needs.
Participate in strategic collaboration with therapeutic area responsible leads, and clinical research and development colleagues to develop strategic IIS guidance documents; support of IIS projects across the portfolio.
Perform basic clinical and laboratory procedures during subject clinic visits such as obtaining medical history, taking vital signs, drawing blood and obtaining other clinical, research, and immunological specimens as required.
This position will have key relationships internally with clinical project teams, marketing and business development, and brand or therapy area team leaders, and externally with regulatory bodies and external service providers.
The Community Clinical Coordinator is responsible for completing comprehensive medication reviews, providing patient education, medication adherence support, clinical assessments, and side effect monitoring for patients referred to the service
In this role, you will process of donor management, allocation of tissues for transplant and research, and recovery according to UNOS, OPTN, AOPO, CLIA, and Indiana Donor Network guidelines, policies and regulations.
Develops and manages clinical protocols and amendments, informed consent forms, training material, case report forms, diary cards, clinical study reports and other clinical documents, and contributes to the development of investigator's brochures.