Study Coordinator I,Technical Operation

Crown Bioscience•Kannapolis, NC

51d

About The Position

Job Summary: 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. Crown Bioscience, a JSR Life Sciences company, is a global contract research organization (CRO) providing discovery, preclinical, and translational platforms to advance oncology and immuno-oncology. Known for their high quality and expansive in vivo, in vitro, and ex vivo preclinical models, they partner with their clients to quantify the efficacy and pharmacological profile of their drug candidate before they move into the clinic. The company is the only preclinical CRO to provide tumor organoid services utilizing HUB technology and has the world’s largest commercially available PDX collection. Additionally, further services available in the areas of high content imaging and a 3D Ex Vivo Patient Tissue Platform, provide greater insights into complex disease pathophysiology. A range of biomarker analysis and applied genomics services are also available to optimize therapeutic benefit. Crown Bioscience helps to deliver superior drug candidates to ensure that patients get the right treatment at the right time. Founded in 2006, Crown Bioscience has 12 facilities in the US, Europe, and APAC. Find out more: www.crownbio.com Crown Bioscience is committed to a diverse and inclusive workplace. Crown Bioscience is an equal opportunity employer and does not discriminate on the basis of race, national origin, gender, gender identity, sexual orientation, protected veteran status, disability, age, or other legally protected status. If you have a disability or special need that requires accommodation, please let us know: [email protected] Headhunters and recruitment agencies may not submit resumes/CVs through this website or directly to managers. Crown Bioscience does not accept unsolicited headhunter and agency resumes. Crown Bioscience will not pay fees to any third-party agency or company that does not have a signed agreement with Crown Bioscience.

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