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Preclinical Project Manager Jobs in Walpole, MA (NOW HIRING)

Project Manager, PMO

Waltham, MA ยท Hybrid

$137K - $147K/yr

... preclinical candidates in development for various psychiatric and neurological disorders. We are proud to have been recognized as an employer of choice by many national organizations. In 2024 and ...

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Preclinical Project Manager information

See Walpole, MA salary details

$42K

$112K

$176.6K

How much do preclinical project manager jobs pay per year?

As of Aug 28, 2026, the average yearly pay for preclinical project manager in Walpole, MA is $111,955.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,600.00 and $134,100.00 per year, depending on experience, location, and employer.

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.

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 cities near Walpole, MA are hiring for Preclinical Project Manager jobs?

Cities near Walpole, MA with the most Preclinical Project Manager job openings:

Infographic showing various Preclinical Project Manager job openings in Walpole, MA as of August 2026, with employment types broken down into 93% Full Time, and 7% Contract. Highlights an 79% In-person, and 21% Remote job distribution, with an average salary of $111,955 per year, or $53.8 per hour.

6475 - IT Project Manager / Project Manager

Verista, Inc.

Cambridge, MA โ€ข Hybrid

$107K - $127K/yr

Full-time

Posted 20 days ago


Job description

Description of Role:

The Project Manager will be responsible for planning, managing, tracking and reporting of all project activities. In this role, the PM will be supporting Research and Preclinical projects - projects will include new implementations as well as enhancements to existing systems/applications. The position sits within the PMO and thus will need to support key project management processes and reporting requirements.

IT Project Manager Responsibilities:

  • Lead the planning, execution, and delivery of projects in accordance with the project timeline and budget; Manage project scope, goals, and deliverables that support project objectives in collaboration with project stakeholders;
  • Develop and maintain project plans, timelines, and budgets, ensuring that project deliverables are completed on time, within budget, and to the required quality standards
  • Manage deliverables and ensure stakeholders are engaged and responsive;
  • Oversee and drive all project team management and controls in accordance client's PMO methodology (e.g., project planning, scope, issue and risk management, decisions tracking, meeting coordination and minutes, etc.)
  • Manage project risks, issues, and dependencies, identifying potential problems and implementing solutions to mitigate them;
  • Monitor projects and utilize client's IT SDLC project processes and artifacts to report on project progress and provide written project status for project reviews.
  • Develop, manage and report on project financials, as required by client;
  • Ensure effective communication and collaboration with cross-functional teams and third-party vendors;
  • Ensure that all project documentation is complete, accurate, and up to date.
  • Support IT security/infrastructure review process for new IT systems, as applicable

Requirements:

  • Experience managing successful IT projects including project dashboard/status updates, stakeholder management, vendor management, timeline management, and tracking of key risks, issues, activities, and deliverables
  • 4+ years working in a regulated pharmaceutical organization, CRO or FSP; must have experience supporting projects in the Research and/or Preclinical domain (e.g. ELN, LIMS, Imagine, Digital Pathology, Instrument Data Capture)
  • 8+ years as a project manager and business analyst
  • Ability to communicate effectively with stakeholders at all levels of a matrix organization
  • Ability to work in a collaborative team environment - willing to pitch in to achieve goals and maintain relationships with business leads, stakeholders, business users, technical team, validation, quality, and vendor resources
  • Ability to work independently and with minimal supervision
  • Demonstrated ability to establish and meet priorities and deadlines
  • Experience with timeline management and resource/capacity management
  • This position is Hybrid - 3 days onsite per week in Cambridge, MA