jobs.pl/Job offers/Research and Development/Project Manager, CRO & CDO
Source: CrawlJobs

Project Manager, CRO & CDO

Full-time On-site work

Publication date: 30/08/2026

At Argenta, we’re more than a company — we’re a global team, dedicated to healthier animals. We believe that when their lives are made better, we're all the better for it. Founded in 2006, we support companies big and small to develop and manufacture health products for pets and livestock. Our trusted, innovative solutions and services cover every stage of the process, from molecule to market. We’re in a unique position. We are the world’s only combined contract research and contract development and manufacturing organization (CRO/CDMO) dedicated to animal health. Argenta is currently looking to fill the role of Project Manager, CRO & CDO at our Shawnee, KS location.

Responsibilities

Develop and manage project plans, define project scope and oversee all phases from initiation to closure; Work with Americas CRO senior leaders to create and manage budgets and timelines to ensure project completion; Establish clear project structures including milestones, risks, dependencies, and performance metrics; Monitor progress and proactively mitigate risks related to scope, cost, timing, and quality; Drive decision-making through structured facilitation and escalation when needed; Ensure facility operates safely and within compliance while special projects are completed; Performs all Company business in accordance with all relevant regulations (e.g. FDA, CVM, OHSA, EPA) and Company policy and procedures. Ensure compliance with all Regulatory agencies; Demonstrates high ethical and professional standards with all business contacts to maintain Argenta, MVS’ excellent reputation in the community; Recommend and implement process improvement activities to improve quality and efficiency; Train and coach personnel within the project scope

Requirements

Bachelors Degree; Experience in an animal health research facility; Understanding of cGMP's as interpreted by the USFDA CVM; Strong analytical skills; Demonstrated organizational skills; Ability to set priorities and schedules so studies runs efficiently; Influence, persuasion, negotiation, conflict resolution skills; Strong understanding of workflow processes; Functional knowledge of Microsoft Office Products; Minimum Experience: Mid-level

Benefits

great benefits; growth opportunities
Apply with employer

Similar offers

All →

Cookie settings

Each purpose is optional and off by default. You can withdraw consent at any time.

Showing offers closest to you