Crown Bioscience


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.


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


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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