Assist with the development of protocol-specific systems and documents including process flows, training manuals, standard operating procedures, and case report forms.
September 06, 2021
Contribute to the development of clinical protocols, informed consent forms, and case report forms.
December 05, 2021
Build influential partnerships across Respiratory and Monitoring Solutions Franchises, including cross-functional Regulatory, Clinical, and Regional Marketing, to ensure the successful deployment and analysis of post-market clinical follow-up activities.
December 26, 2021
Participate in training to enhance knowledge base.
December 27, 2021
Develop and deliver technical training on GCPs, protocols, database, compliance, device accountability, adverse event reporting, study investigation protocols, amendments, regulatory documentation requirements as well as training and proctoring new employees on trial and study related activities.
January 20, 2022
Provides field support for various clinical research studies by selecting sites, performing activation duties, setting up protocols, providing training, helping to enroll participants, ensuring quality data acquisition and performing study closure activities.
February 02, 2022