JOB SUMMARY:
The purpose of the Study Coordinator position is to support the execution of in vitro and in vivo pharmacology studies, by coordinating the technical execution of projects this includes scheduling, creating and distributing study-related documents, as well as hands on assistance. The Study Coordinator assist Study Directors in composing and reviewing study protocols and study reports, monitoring the execution of the study, analyzing the data and meeting study timelines.
PRIMARY RESPONSIBILITIES:
Coordinate with in-house staff for animal studies
Provide drug formulation if needed
Support study project time-lines and protocol execution
Assist in creation and distribution of study-related documents and other study tools
Sets up Studylog for new studies
Contribute to study planning, scheduling, initiation, and study-closure processes supporting the Study Director
Provide hands on support for study milestones
Track and monitor progress and quality metrics and data analysis
Assist with study reports and presentations
May support Study Directors with client communications
Provide quality checks of study plans and reports, assisting QA with the development and implementation of corrective actions for addressing noncompliance issues
Conduct work activities in compliance with all relevant regulations including ethics, environmental health and safety, financial, human resources, SOPs, and general business policies, requirements and objectives
EDUCATION, KNOWLEDGE, AND EXPERIENCE REQUIREMENTS:
Requires a Bachelor’s degree in a scientific discipline or equivalent experience
Requires 2+ years of experience in inflammation related animal studies
Prefer experience in a CRO setting and ability to manage customer projects and customer interactions
Demonstrated experience leading teams and driving results
Preferred experience and knowledge with translational research in inflammation
Preferred animal handling experience in a laboratory setting
Willing and able to work under the pressure of deadlines and find solutions to meet timelines
Ability to work across teams by being a flexible team player with strong communication and interpersonal skills
Willing and able to work within a Quality System with oversight by QA and other regulatory bodies
Exceptional organizational and time-management skills
Ability to multi-task with a high degree of professionalism and diplomacy
Proficient in Microsoft Office and preferred experience with GraphPad Prism
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