Project Manager, CRO & CDO

Argenta

$80K — $100K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree required
  • Experience in an animal health research facility
  • Understanding of cGMP's per USFDA CVM standards
  • Strong analytical skills required
  • Excellent organizational skills
  • Ability to prioritize and schedule effectively
  • Demonstrated influence and conflict resolution skills
  • Functional knowledge of Microsoft Office Products

Responsibilities

  • Develop and manage comprehensive project plans from inception to closure
  • Collaborate with CRO senior leaders on budget and timeline management
  • Establish project structures with clear milestones and performance metrics
  • Monitor project progress and proactively address scope, cost, and quality risks
  • Drive decision-making through facilitated discussions
  • Ensure regulatory compliance during special project completions
  • Implement and recommend process improvements for efficiency
  • Train and mentor team members within project scope

Benefits

  • Strong company culture that values employee input
  • Opportunity to work in a rapidly expanding global business
  • Supportive work environment with enjoyable colleagues
  • Great benefits and growth opportunities
Full Job Description
Argenta is currently looking to fill the role of Project Manager, CRO & CDO at our Shawnee, KS location. Key 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
About You:
  • 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
Argenta has strongly embedded company values which is key to who we are and how we deliver. We offer an opportunity to work for a successful and rapidly expanding global business where your input will be valued. At Argenta we are a hard-working group who really enjoy the people we work with each day. That is why we support our people through a strong culture, great benefits, and growth opportunities.

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