Study Coordinator I,Technical Operation

Crown Bio • Kannapolis, NC

1d

About The Position

The purpose of the Study Coordinator I 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 providing hands-on assistance. The Study Coordinator will provide operational input to Study Directors (Scientists) on study protocol design, and they will serve as a team leader for a group of Research Associates whose primary responsibility is executing the hands-on portion of any given study.

Requirements

• Bachelor's degree in a scientific discipline and 1+ years of experience in oncology related animal studies.
• Demonstrated experience leading teams, strong communication skills, maintaining organization, and driving results
• Willing and able to work under the pressure of deadlines and find solutions to meet timelines.
• Able to work under pressure to meet deadlines
• 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.
• Ability to work independently and collaboratively in a fast-paced, team-oriented environment.

Nice To Haves

• CRO industry experience and ability to manage a high volume of customer projects
• Preferred experience and knowledge with translational research in oncology
• Preferred Animal handling/ In-vivo experience in a laboratory setting
• Preferred Animal welfare/ IACUC knowledge
• Preferred experience with SmartSheet, Study Director, Outlook, and Microsoft teams

Responsibilities

• Coordinate the successful execution of client studies with various internal departments
• Create and distribute study-related documentation and other materials for required for execution
• Support Study Directors (Scientists) in scientific protocol development
• Schedule studies with operational flexibility while maintaining competitive timelines
• Maintain a daily schedule of all tasks that must be executed by Research Associates
• Monitor and assure quality of data collection
• Provide hands-on In-vivo support for study milestones
• Provide drug formulation, if needed
• Ordering study-related materials
• 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

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Number of Employees: 251-500 employees