requirements. Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory... submissions. Support the preparation of study-related materials, such as informed consent forms and case report forms...
Study Support Assistant ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re... to shape the future of clinical development We are looking for a Study Support Assistant for the Site Activation department...
of clinical development We are currently seeking a Study Start Up Associate II to join our diverse and dynamic team. As a Study... stakeholders to obtain necessary approvals and authorizations for study initiation. Managing and maintaining comprehensive...
development and implementation. Partner with Research & Opertations in order to identify new trade areas to work. Analice the... consistently, through from assigned areas. Travel to trade areas, and negotiate all aspects of the real estate transaction...
. May have to work evenings & weekends. Availability to travel locally and internationally. Our progress will give... projects inspections which cause is not known, evaluation and study of movements and times for a better balance in production...
with protocols and regulatory requirements. Maintain and organize clinical trial documentation, including study files, essential... documents, and regulatory submissions. Support the preparation of study-related materials, such as informed consent forms...
management of clinical trial sites by assisting with site monitoring activities, ensuring compliance with study protocols... monitoring of clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice...
with protocols and regulatory requirements. Maintain and organize clinical trial documentation, including study files, essential... documents, and regulatory submissions. Support the preparation of study-related materials, such as informed consent forms...
guidelines, and industry standards. Coordinate study activities including site initiation, patient recruitment, data... trials. Maintain comprehensive study documentation and records, ensuring compliance with applicable regulations...
will be required to perform some work onsite at the listed location, with some travel to other cities from time to time. This is at the hiring... Regional Manager of the SoCal and Latin America team. Our team thrives in a remote work environment, with the exciting...