What are the responsibilities and job description for the Specialist: Study Management position at Clinglobal Group?
Departmental Objective
The objective is to deliver efficient and high-quality research that in line with compliance and meets timelines.
Primary Job Purpose
Serve as lead support to a Principal Specialist: Study Management as needed on studies as appointed by Test Facility Management.
Job Specific Duties and Responsibilities
• Study master file administration, including, but not limited to the preparation and close-out of files, raw data reviews, and data management tasks
• Assist in drafting study proposals, protocols, and reports
• Assist in drafting research approval applications to IACUC and IBC
• Coordinate study related activities with other applicable departments as necessary
• Coordinate and/or perform study setup: preparation and review of facility/study logs, study rooms/cages, animal selection and acclimation, environmental enrichment, scheduling study activities, and other related duties as needed
• Coordinate and/or participate in day-to-day research activities such as dose preparation, administration, observations, sample collection, and other related research tasks
• Communicate study progress to the Principal Specialist: Study Management & Study Sponsor when
requested
• Timely reporting of study adverse events to the Principal Specialist: Study Management.
Qualification, Training, and Experience Requirements
•A bachelor's degree combined with 7 or more years of relevant hands-on clinical animal research experience.
