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Preclinical Cro Project Manager Jobs (NOW HIRING)

Argenta

Project Manager, CRO & CDO

Shawnee, KS · On-site

Argenta is currently looking to fill the role of Project Manager, CRO & CDO at ourShawnee, KS location. Key Responsibilities: * Develop and manage project plans, define project scope and oversee all ...

Argenta

Project Manager, CRO & CDO

Shawnee, KS · On-site

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 ...

Argenta

Project Manager, CRO & CDO

Shawnee, KS · On-site

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 ...

Actalent

PK/ADA Scientist

Auxvasse, MO · On-site

Manage assigned projects and proactively order and coordinate appropriate materials and resources ... Proven experience in a preclinical/CRO environment working under GLP and ICH guidelines. * Strong ...

Katalyst CRO

IT Project Manager

Portsmouth, NH · On-site

$100K - $118K/yr

Katalyst CRO is a company focused on delivering IT solutions, and they are seeking an IT Project Manager to oversee the planning and execution of IT projects. The role involves managing global teams ...

Azenta US, Inc.

$150K/yr

Work closely with internal teams (project management, marketing, scientific experts & account ... CRO/scientific solutions. * Domain Expertise: Experience selling early-stage preclinical services ...

Azenta US, Inc.

$150K/yr

Work closely with internal teams (project management, marketing, scientific experts & account ... CRO/scientific solutions. * Domain Expertise: Experience selling early-stage preclinical services ...

Pharmaron

In Vivo Operations Specialist

Carlsbad, CA · On-site

$80K - $100K/yr

The In Vivo Operations specialist will also function as a study manager assisting the study ... preclinical, CRO, or vivarium environments * Experience coordinating operations or projects in fast ...

Pharmaron

In Vivo Operations Specialist

Carlsbad, CA · On-site

$80K - $100K/yr

The In Vivo Operations specialist will also function as a study manager assisting the study ... preclinical, CRO, or vivarium environments * Experience coordinating operations or projects in fast ...

Pharmaron

In Vivo Operations Specialist

Carlsbad, CA · On-site

$80K - $100K/yr

The In Vivo Operations specialist will also function as a study manager assisting the study ... preclinical, CRO, or vivarium environmentsExperience coordinating operations or projects in fast ...

PSI CRO

Regional Project Lead

At PSI CRO, our Regional Project Leads are trusted leaders who drive the successful delivery of clinical trials across multiple countries. You'll partner with Project Managers, CRAs, sponsors, and ...

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Preclinical Cro Project Manager information

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$38.5K

$102.7K

$162K

How much do preclinical cro project manager jobs pay per year?

As of Sep 13, 2026, the average yearly pay for preclinical cro project manager in the United States is $102,682.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,500.00 and $123,000.00 per year, depending on experience, location, and employer.

What is a preclinical CRO project manager?

A Preclinical CRO Project Manager is a professional responsible for overseeing and coordinating preclinical research studies conducted by a Contract Research Organization (CRO). They manage timelines, budgets, and resources to ensure that studies evaluating the safety and efficacy of new drugs or medical devices are completed according to client specifications and regulatory standards. Their role involves communicating with clients, leading multidisciplinary teams, and ensuring that all project milestones are met efficiently and compliantly.

What are the key skills and qualifications needed to thrive as a preclinical CRO project manager?

To thrive as a Preclinical CRO Project Manager, you need a strong background in life sciences, project management experience, and knowledge of preclinical drug development processes, often supported by an advanced degree (e.g., MSc or PhD). Familiarity with laboratory information management systems (LIMS), project management software, and regulatory standards like GLP is typically required. Excellent communication, leadership, and organizational skills are essential for coordinating multidisciplinary teams and managing client relationships. These abilities ensure successful project delivery, regulatory compliance, and client satisfaction in a highly regulated, deadline-driven environment.

What are the main challenges a preclinical CRO project manager faces when coordinating studies across multiple scientific teams?

A Preclinical CRO Project Manager often navigates the complexities of coordinating multidisciplinary teams, such as pharmacology, toxicology, and bioanalytical groups, each with their own timelines and priorities. Balancing client expectations, regulatory requirements, and shifting project scopes can be challenging, especially when studies involve multiple sites or international partners. Successful managers are adept at proactive communication, risk management, and problem-solving to ensure projects stay on track and deliverables meet quality standards. This role also requires flexibility to adjust plans swiftly in response to unexpected scientific or logistical hurdles.

What are popular job titles related to Preclinical Cro Project Manager jobs?

For Preclinical Cro Project Manager jobs, the most frequently searched job titles are:

Infographic showing various Preclinical Cro Project Manager job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution, with an average salary of $102,682 per year, or $49.4 per hour.

Project Manager, CRO & CDO

Shawnee, KS • On-site

Argenta
11 - 50 employees
Learn more about Argentaexternal

Full-time

Re-posted 24 days ago

Job description

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.

Our uniqueness means:

We are ambitious, growing and building a 'one team' culture, guided by our values.


    • We are team players;
    • We are doers;
    • We are customer-centric;
    • We are innovators.


We value diversity, as a global company, we get the richness of working with different people in different places whether it be location, stages of their career, their development, their role. We believe that when everyone works together and puts their best "paw" forward we will make the lives of the animals we care for, better.

With bases in New Zealand, the US, the UK and Europe, our 900+ colleagues are driven by our partnership approach and purpose: Healthy Animals. Let's Make It Happen, Together.

TEAM PLAYERS who want to DO great work and find INNOVATIVE ways to make animals lives better through our CUSTOMER CENTRIC efforts should apply.

Argenta is currently looking to fill the role ofProject Manager, CRO & CDOat ourShawnee, KSlocation.

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 safelyand within compliance while special projects are completed
  • Performs all Company business in accordance with allrelevantregulations (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 contactstomaintainArgenta,MVS'excellent reputation in the community
  • Recommend and implement process improvement activities to improve quality and efficiency
  • Train and coach personnelwithin the project scope

About You:

  • Bachelors Degree
  • Experience in ananimal health research facility
  • Understanding of cGMP's as interpreted by theUSFDACVM
  • Strong analyticalskills
  • Demonstrated organizational skills
  • Ability to set priorities and schedules sostudiesrunsefficiently
  • Influence, persuasion, negotiation, conflict resolution skills
  • Strong understanding ofworkflowprocesses
  • 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.

Argenta is an equal-opportunity employer

To find out more about Argenta, click here: www.argentaglobal.com

Apply