Inotivco

Study Coordinator

WestminsterFull time$26 - $33 / hourPosted 12 days ago
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 Responsibilities and DutiesCorporateFollow all SOPs and other applicable company policies and proceduresMaintain confidential informationGeneral Interact and communicate with clients, vendors, other employees, and the community in a professional mannerSupport and participate in company initiatives as directedMaintain thorough knowledge of facility SOPs, policies, protocols, etc.Adhere to all safety regulations and proceduresProvide assistance or support to other Inotiv sites as necessaryPerform other duties as assignedSpecificMaintain and submit study initiation materialsOrder all applicable supplies for studiesCommunicate with other coordinators to schedule study activitiesEnsure creation of data sheetsConfirm laboratory math for test article and disease induction formulationCommunicate with formulations team regarding timeline and materials neededAssist with in-life study conduct, as needed, and as trainedComplete training requirements as assigned and maintain appropriate training documentationPerform periodic review of all applicable SOPs to ensure accuracy and confirm procedures are being performed according to SOPs. Participate in SOP writing, reviews, and revisions, as neededMaintain compliance with all policies and proceduresEnsure compliance with USDA, AAALAC, OLAW, GLPs and other applicable regulationsPerform quality checks, reviews, and formatting on all Inotiv documents (e.g. protocols, amendments, deviations, reports, tables, etc.)Develop and maintain study protocol, report, and data table master templatesProvide back-up support for Study Directors as neededAid in protocol and any protocol amendment or deviation preparation and distributionPrepare and review raw data collection forms and review for adherence to protocol, both prior to study start and after study completionReview raw data collection and in-life study conductAssist to prepare a complete study file for archival following finalization of reportAssist to ensure that study samples and test articles are shipped appropriately, on schedule, and documented in the study filePerform other duties as assignedPosition RequirementsEducation and experienceAt a minimum, the Study Coordinator must have a Bachelor's degree in life sciences or other directly related field or degree with comparable coursework and a minimum of three years in a relevant pharmaceutical settingThe Study Coordinator must have a minimum of one year experience with animals and animal handlingSkills and abilitiesA working knowledge and awareness of general laboratory proceduresCustomer focused, results driven, communicative, and collaborative enabling effective customer satisfaction, including problem solving, fostering positive relationships, and proactive communicationAbility to adhere to and manage in accordance with the Code of Federal Regulations proceduresExperience in the use of computer software applications (e.g., Word, Outlook, Excel)Possess strong skills for editing the format, style and langua...