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Preclinical Project Manager Jobs (NOW HIRING)

Research Project Manager

Phoenix, AZ · On-site

$67K - $86K/yr

As a Research Project Manager, you will provide comprehensive oversight and leadership for the ... Coordinate preclinical project work activities among internal departments and stakeholders ...

Research Project Manager

Phoenix, AZ · On-site

$67K - $86K/yr

Coordinate preclinical project work activities among internal departments and stakeholders ... Work with biorepository and veterinary managers to ensure that materials for pre clinical study ...

The Study Coordinator provides critical operational and project management support to the Study Director in GLP-regulated preclinical studies for Neuralink devices. This role handles the majority of ...

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Preclinical Project Manager information

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$38.5K

$102.7K

$162K

How much do preclinical project manager jobs pay per year?

As of Jun 16, 2026, the average yearly pay for preclinical 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.

How does a Preclinical Project Manager typically coordinate with cross-functional teams during a drug development project?

A Preclinical Project Manager works closely with scientists, regulatory affairs, toxicology, and external vendors to ensure all preclinical studies are executed on time and within budget. They facilitate regular meetings to align project milestones, address challenges, and manage documentation for compliance. Effective communication and proactive issue resolution are key, as the role often requires balancing the needs of diverse stakeholders while keeping the overall project timeline on track.

What are the key skills and qualifications needed to thrive as a Preclinical Project Manager, and why are they important?

To thrive as a Preclinical Project Manager, you need a solid background in life sciences or pharmaceutical research, often with an advanced degree and experience managing preclinical studies. Familiarity with project management tools, regulatory guidelines (such as GLP), and software like Microsoft Project or similar platforms is typically required. Strong organizational, leadership, and communication skills are vital for coordinating cross-functional teams and ensuring project timelines are met. These skills and qualifications are crucial for efficiently advancing drug candidates through preclinical development while ensuring compliance and project success.

What does a Preclinical Project Manager do?

A Preclinical Project Manager oversees the planning, coordination, and execution of preclinical research projects that typically involve laboratory and animal studies before clinical trials in humans can begin. They work closely with scientists, regulatory teams, and stakeholders to ensure that studies are conducted according to protocols, timelines, and regulatory requirements. Their responsibilities include managing budgets, resources, and communication among various teams to advance drug candidates or medical devices through the early stages of development. Effective Preclinical Project Managers help ensure that projects meet scientific and business objectives, and that all data generated is reliable and compliant with industry standards.
More about Preclinical Project Manager jobs
What cities are hiring for Preclinical Project Manager jobs? Cities with the most Preclinical Project Manager job openings:
What states have the most Preclinical Project Manager jobs? States with the most job openings for Preclinical Project Manager jobs include:
Infographic showing various Preclinical Project Manager job openings in the United States as of June 2026, with employment types broken down into 95% Full Time, 4% Part Time, and 1% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $102,682 per year, or $49.4 per hour.
Preclinical Project Manager

Full-time

Posted 29 days ago


Job description

Company Description

A Few Words About Us
Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

Preclinical Project Manager

  The Project Management Office (PMO) is part of the Janssen R&D organization. Their mission is to bring the right products to patients by driving R&D Programs and portfolio decisions through integrated time, scope risk, resources and people management. Within Discovery Sciences, PD&S is responsible for the assessment of the preclinical safety profile of internally and externally generated small molecules (and vaccines) starting in the discovery phase up to post-approval support. Among the major, critical capabilities are integrated drug development support and global submissions, pharmacokinetics, dynamics and metabolism, bio-analysis, isotope synthesis, PK/PD modeling, toxicology/pathology, mechanistic and investigative safety and laboratory animal medicine support.

The Senior Manager, PD&S Project Manager provides project management support to Pre-Clinical Development (PCD) Leaders and PCD teams. This includes:

  building project timelines developing and analyzing scenarios, risk assessment and mitigation planning developing project budgets developing resource needs (FTE's = Full Time Equivalents) with PD&S functions tracking and reporting actualization of project timelines, budgets and FTE's. The Senior Manager, PD&S Project Manager provides support for continuous forecasting, quarterly financial updates, development of Business Plan Budgets and FTE's and preparation for Governance Meetings. He/she is a member of the PD&S team (sub team of Compound Development Team) and works with the team and with PD&S functions to facilitate successful project execution, achievement of key deliverables and of budget and FTE goals. As a member of the Project Management Team he/she supports cross-functional planning, budgeting and resourcing activities. The primary responsibilities include: be an active member of assigned PD&S Teams build and maintain project plans Develop forecasts regarding project resource needs (OOP's and FTE's) Track actual expenses and FTE's against forecasts Liaise with project finance, program management and customer groups from Janssen R&D organization.

Qualifications

Qualifications Education :

Bachelors Degree in Scientific Discipline (A Master's Degree is highly preferred).

Experience :

Minimum of 6-8 years experience in the pharmaceutical industry. Knowledge of Pharmaceutical Development and Clinical Development. Experience in Project Management. Capability in the Microsoft suite of business software including MS Project, Visio and Excel. Experience in working in multinational/multicultural organizations. Prior Pre-Clinical Development / PD&S experience (preferably minimum of 2 years) Knowledge of project management tools and techniques. Prior experience with Planisware is desirable Critical Competencies Communication Customer focus Collaboration and teaming Be able to work in a highly matrixed organization Results and performance driven

Additional Information

RESPONSIBILITIES: 


Candidates will work with fellow scientists to designing and executing experiments including small-scale studies, and pilot plant and manufacturing studies in a variety of types and scales of equipment from bench top to pilot-scale, and, as required, technology transfer and validation in commercial plants. 

Based on the analyses of these studies, these positions will be expected to develop and test new hypotheses to improve fundamental understanding of the chemical and biochemical processes, including bio-conjugation or large and small molecule combinations. 

This position will support process validation, quality by design, regulatory approaches, and quality systems 

This position requires a highly motivated individual with the ability to work closely with other members of the laboratory and the department in a matrix environment. 

This position will also collaborate with the pilot plan and manufacturing staff on experimental studies, clinical manufacturing, and process validation, including work with external contract manufacturing organizations 



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About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996