provantis

The Quality Control and Report Coordinator Level I position is responsible for the review, Quality Check, and organization of all Study data collected manually and electronically. They will thoroughly inspect the data for consistency, completeness, and compliance to the Study Protocol, Good Laboratory Practice (GLP), Standard Operating Procedures (SOPs), and...

Inotiv seeks a Quality Control and Report Coordinator Level I to review and organize study data, ensuring consistency, completeness, and GLP/SOP compliance. You will assist in compiling data tables and preparing required documentation across Provantis, Ascentos, and related systems. The role emphasizes meticulous data handling, collaboration with histology...

 Title: Study Assistant Location: Concord, OH (on-site)Reports To: Study Support Team LeaderCompanyFrontage Laboratories Inc. is an award winning, publicly listed, full-service CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada, and China, growing significant YoY growth. Our core competencies include...

Job Title Scientific Research Associate Department Pathology Reports To Director of Pathology Job Overview The Scientific Research Associate will work across Virscio to review study protocols, support and set up study specific electronic data capture systems (Provantis, Excel, Word), manage study scheduling, pull out and organize data to enable downstream...

Company DescriptionIRI believes in commitment, Integrity and strategic workforce solutions.Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled...

This role provides scientific and strategic leadership to embed AI/ML-enabled pathology and digital pathology capabilities into Takeda’s nonclinical research workflows.This role will work with the NCSP iDigPath team to advance AI/ML applications that enable quantitative, high-content analysis of pathology data to improve sensitivity, reproducibility, and...

Overview The qualified candidate is responsible for organizing, conducting, and reporting non-GLP rodent toxicology, investigative, and pharmacokinetics/toxicokinetic (PK/TK) studies that support drug discovery and development. An understanding and comprehension of SOPs, techniques, nomenclature etc. are expected as they relate specifically to job...

We are seeking a Quality Assurance (QA) Auditor to support our federal contract with the National Institute of Environmental Health Sciences (NIEHS). The QA Auditor will ensure the accuracy, integrity, and compliance of toxicological research studies, with a focus on rodent models (mice and rats). This position requires strong auditing and QA skills,...

The Quality Control and Report Coordinator Level I position is responsible for the review, Quality Check, and organization of all Study data collected manually and electronically. They will thoroughly inspect the data for consistency, completeness, and compliance to the Study Protocol, Good Laboratory Practice (GLP), Standard Operating Procedures (SOPs), and...

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use.  I further attest that all information I submit in my employment application is true to the best of my knowledge.Job...

Who are we, and what do we do?At Corteva Agriscience, you will help us grow what’s next. No matter your role, you will be part of a team that is building the future of agriculture – leading breakthroughs in the innovation and application of science and technology that will better the lives of people all over the world and fuel the progress of...

Overview   The qualified candidate is responsible for organizing, conducting, and reporting non-GLP rodent toxicology, investigative, and pharmacokinetics/toxicokinetic (PK/TK) studies that support drug discovery and development. An understanding and comprehension of SOPs, techniques, nomenclature etc. are expected as they relate specifically to job...

Director, GLP Quality Assurance & ComplianceBuilding a Culture of Quality & Compliance in a Leading In Vivo Research FacilityCompany OverviewWe are a pioneering research organization dedicated to translational medicine, bridging the gap between research and real-world applications to improve human health. As we expand our in vivo research capabilities,...

Manager, Study Coordination & Quality ControlJoin a team driven by science, powered by people, and committed to improving lives. A GLP public CRO is seeking an experienced and passionate Manager, Study Coordination & Quality Control, to lead its Preclinical Operations team. In this critical leadership role, you will oversee project execution, ensure quality...

Senior Animal Research TechnicianScience & ResearchBirmingham, Alabama, USAdded - 10/12/2025Our client is a leader in the life sciences and biomedical research industry, driving innovation through advanced laboratory techniques and rigorous scientific methods.Title: Sr Animal Lab TechLocation: Jefferson County, AlabamaJob type: Contract - hirePay rate: ...

Application Administrator - Provantis   Southern Research + You Discover a career where your work truly matters. Southern Research has been translating science into real-world solutions since 1941. Join our innovative team and enjoy benefits like medical, dental, vision, 401(k) match, life insurance, PTO, an employee assistance program, and...

Position: Scientific Writer II, Preclinical Research Pay Range: $60k - $75k Location: Carlsbad, CA (On-site) About Pharmaron Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 locations in the US, UK, China, and...

The Scientific Research Associate will work across Virscio to review study protocols, support and set up study specific electronic data capture systems (Provantis, Excel, Word), manage study scheduling, pull out and organize data to enable downstream analysis, QC draft reports, and draft SOPS and report templates. The Scientific Research Associate may work...

The Scientific Research Associate will work across Virscio to review study protocols, support and set up study specific electronic data capture systems (Provantis, Excel, Word), manage study scheduling, pull out and organize data to enable downstream analysis, QC draft reports, and draft SOPS and report templates. The Scientific Research Associate may work...

Study Coordinator Title: Study CoordinatorLocation: Chicago, IL (on-site)Reports to: Technical Report Supervisor Full-timeFrontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China. Our core competencies include drug metabolism,...