Study Coordinator

Responsibilities and Duties Corporate Follow all SOPs and other applicable company policies and procedures Maintain confidential information General Interact and communicate with clients, vendors, other employees, and the community in a professional manner Support and participate in company initiatives as directed Maintain thorough knowledge of facility SOPs, policies, protocols, etc. Adhere to all safety regulations and procedures Provide assistance or support to other Inotiv sites as necessary Perform other duties as assigned Specific Maintain and submit study initiation materials Order all applicable supplies for studies Communicate with other coordinators to schedule study activities Ensure creation of data sheets Confirm laboratory math for test article and disease induction formulation Communicate with formulations team regarding timeline and materials needed Assist with in-life study conduct, as needed, and as trained Complete training requirements as assigned and maintain appropriate training documentation Perform 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 needed Maintain compliance with all policies and procedures Ensure compliance with USDA, AAALAC, OLAW, GLPs and other applicable regulations Perform 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 templates Provide back-up support for Study Directors as needed Aid in protocol and any protocol amendment or deviation preparation and distribution Prepare and review raw data collection forms and review for adherence to protocol, both prior to study start and after study completion Review raw data collection and in-life study conduct Assist to prepare a complete study file for archival following finalization of report Assist to ensure that study samples and test articles are shipped appropriately, on schedule, and documented in the study file Perform other duties as assigned Position Requirements Education and experience At 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 setting The Study Coordinator must have a minimum of one year experience with animals and animal handling Skills and abilities A working knowledge and awareness of general laboratory procedures Customer focused, results driven, communicative, and collaborative enabling effective customer satisfaction, including problem solving, fostering positive relationships, and proactive communication Ability to adhere to and manage in accordance with the Code of Federal Regulations procedures Experience in the use of computer software applications (e.g., Word, Outlook, Excel) Possess strong skills for editing the format, style and language of draft protocols, spreadsheets and reports Excellent written and verbal communication skills An attitude for quality, an eye for detail and the ability to read and follow written instructions Ability to interact with scientific staff at all levels Performance Requirements General Ability to read, write, speak, and understand English Able and willing to work a flexible schedule according to study needs Physical activity Moderate physical activity: Prolonged periods of sitting at a desk and working on a computer May occasionally lift and/or move objects Able to wear PPE (Personal Protection Equipment) as required Working Conditions Work is normally performed in a typical interior office or laboratory environment Work may require use of PPE due to exposure to potentially dangerous materials and situations Noise level is usually moderate as commensurate with a typical office environment Salary Range: $26.00-$33.00 per hour, adjusted according to the level of the role and the candidate's relevant experience and/or education. Salary will be commensurate with experience and responsibilities. Benefits: Health and dental coverage, short- and long-term disability, paid time off, paid parental leave, 401(k), and more. Position Status: Open until filled. #LI-JM1 #LI-Onsite *This position could be offered at different levels for candidates who qualify with a combination of advanced levels of education and/or years of experience. The salary range will adjust along with the level of the role to match the person's relevant experience and/or education level. At Inotiv, our work helps advance the development of new medicines and therapies that can improve people's lives. As a leading global contract research organization (CRO), we partner with researchers to tackle complex scientific challenges, drive innovation, and help build a healthier, safer world. Bringing together scientists, researchers, technical experts, and business professionals, we provide the expertise and collaboration needed to move research forward. Our people make this work possible, and we value the knowledge, ideas, and contributions each person brings to the team. Whether you are starting your career or bringing years of experience, Inotiv offers opportunities to learn, grow, and play a meaningful role in advancing treatments for patients around the world. Salary will be commensurate with experience and responsibilities. Benefits include health and dental coverage, short- and long-term disability, paid time off, paid parental leave, 401K, and more! Inotiv is an Equal Opportunity Employer. It is our policy to provide a fair and equal employment opportunity to all persons, regardless of age, race, color, religion, sex, gender, gender identity, gender expression, sexual orientation, genetic information, disability, national origin, veteran status, or any other basis prohibited by law. This policy governs all aspects of employment, including selection, job assignment, compensation, discipline, termination and access to benefits and training.