Quality Control Reports Coordinator I

BAS EVANSVILLE INC; Mount Vernon (IN); On-site; USD 45,000 - 65,000; Full time

Benefits offered by this job

Health and dental coverage

Paid time off

401K

Paid parental leave

Disability insurance

Job summary

Inotiv in Mount Vernon, Indiana, seeks a Quality Control and Report Coordinator I to review and organize study data, ensuring compliance with GLP, SOPs, and protocols. The role focuses on data quality, data table generation, and coordination with Histology and other departments.

Responsibilities include thorough data checks in Provantis or Ascentos, preparing tables, supporting room and animal data logs, and maintaining documentation.

Qualifications

• Associate’s Degree or higher in related sciences and/or up to a year of experience in research as a Laboratory Animal Technician or Quality Assurance/Quality Control.

Responsibilities

• Perform thorough review/Quality Check of raw data and electronically entered information for consistency, completeness, and compliance with Protocols and SOPs.

Skills

Attention to detail

Time management

Documentation

Data interpretation

Education

Associate’s Degree or higher in related sciences

Tools

Excel

Word

PowerPoint

Adobe Acrobat PDF

Provantis

Ascentos

LIMS

Master Control

PDS

Microsoft Access

Job description

The Quality Control and Report Coordinator I position is responsible for the review, Quality Check, and organization of all Study data that is manually and electronically collected. They will thoroughly inspect the data for consistency, completeness, and compliance to the Study Protocol, Good Laboratory Practice (GLP), Standard Operating Procedures (SOPs), and other applicable regulations. Level I will also assist in compilation and generation of this collected data into necessary Data Tables, as needed.First Shift - On-sitePosition Responsibilities and Duties:Perform a thorough review/Quality Check of raw data and electronically entered information within the Database (Provantis or Ascentos) for consistency, completeness, accuracy and compliance with Protocol, SOPs, guidelines and regulationsVerify and address applicable findings from raw data or LIMS and coordinate responses from the appropriate personnelReview Study Protocols, Amendments, schedules, and calendarsUnderstand, apply, and maintain adherence to GLP regulations, SOPs and Study Protocols and AmendmentsCollate and organize raw data records within Study bindersUnderstand the purpose and procedure of all raw data formsGenerate and access information needed within the appropriate Database (Provantis or Ascentos)Efficiently and accurately generate Data Tables within the appropriate Database (Provantis or Ascentos), as neededUpon request from the Histology Department and/or other personnel, compile Data Tables with information that has yet to be thoroughly reviewed or Quality Checked, which will subsequently be viewed by Pathologists.Prepare the appropriate corresponding Table and/or Appendix key pages, as needed by Clinical PathologyAssist with maintenance, review/Quality Check, filing and other processes pertaining to Room Maintenance Logs, Animal Data Collection Logs, and other Facility RecordsMaintain a strong and positive working relationship with all departments.Participate in Study initiation meetingsPerform other duties as assigned by Supervisor or appropriate personnelPosition Requirements:Preferred Education and ExperienceAssociate’s Degree or higher in related sciences and/or up to a year of experience in research as a Laboratory Animal Technician or Quality Assurance/Quality ControlTools, Equipment, & Other Resources UsedVarious software applications sustained by a WindowsTM Microsoft platform (Excel, Word, PowerPoint, etc.), and Adobe Acrobat – Portable Document Formatting (PDF)Enterprise Service Management (ESM), Master Control, Watson Laboratory Information Management System (LIMS), Projects Database System (PDS), Provantis, Ascentos, and other DatabasesMicrosoft Access (Outlook, Teams, Dynamics365, etc.)Performance Requirements:*Characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.General AbilitiesAbility to follow strict timelinesAbility to demonstrate strong organizational skillsAbility to pay close attention to detailAbility to perform accurate, concise documentation and accurately proofread documents or dataAbility to work with critical reporting software systems (Microsoft Word, Excel, Adobe PDF, Provantis, Ascentos, etc.) and scanned documents and image filesAbility to interact respectfully and professionallyAbility to adhere to the SOPs and guidelines that protect the integrity of confidential informationPhysical ActivityThis position will require frequent sitting, screen/monitor use and studious activities for extended periods of timeMay require additional hours/overtimeMay require at times reaching while sitting/standing, walking, standing, carrying, lifting (max. 20 50 lbs.), gripping and twisting hand movements, finger control and other general repetitive motions and may require ability to walk over rough terrainPotential Working ConditionsPotential exposure to animal dander and/or materialAbility to work in an environment with mild/moderate noise level or distractionPotential involvement with radiant/electrical energy, solvents, grease, oil, irritants, acids, bases, and other hazardous chemicals, electro-mechanical hazards, flammable materials and biohazards. Due to exposure to hazardous biological materials (which may include HIV positive specimens), immunization to diseases may be requiredMantoux TB test with negative result may be requiredMaintenance of personal protection through the use of latex or nitrile gloves, dust mask and/or respirator, and safety glasses may be required#LI-MP1 #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.