Clinical Project Coordinator

Overview The Clinical Project Coordinator I supports the organization of study-related activities. Establishes study sample management and tracking, study supply inventory and management, and ensures current and complete internal and external data collection. Identifies and assists in solving problems that arise during a clinical study. Responsibilities Coordinates tasks as directed by study leads. Tasks may include: Maintaining the study file. Communicating found or potential problems to study lead or per Communication/Study Plan. Perform quality control checks. Draft and assist in the development of study documents for study lead review. Study metrics tracking and reporting. Sample management tasks. Qualifications Bachelor's degree in life science or related field, or four years of relevant equivalent work experience. Relevant experience in laboratory or clinical study discipline. High attention to detail and great oral/written communication skills. Ability to work well in a cross functional team environment. Experience with Microsoft 365 programs. Physical Requirements Carrying, Communication, Coordinating, Analyzing. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is frequently required to sit; talk; or hear. The employee is occasionally required to stand; walk; use hands to finger, handle, or feel; reach with hands and arms; and stoop; kneel; or crouch. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision and depth perception. Eligibility Applicant must be a (i) U.S. citizen or national, (ii) U.S. lawful, permanent resident (aka green card holder). Compensation and Location We take geographic location into account when determining base salary to ensure equitable and competitive compensation. #J-18808-Ljbffr