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Preclinical Project Manager Jobs (NOW HIRING)

The Preclinical Education component is divided into the teaching of the Basic Sciences and the ... manage and organize daily tasks independently and with a team while balancing multiple projects and ...

Minimum 2+ years of pharmaceutical/biotechnology industry experience including products in preclinical and clinical development (Phase 1-3) * Entry level of project management experience with ...

Senior Project Manager

San Diego, CA · On-site

$88K - $115K/yr

Oversee the project management activities, including addressing clients' inquiries, preparing ... Strong understanding of drug discovery and development processes, particularly in preclinical ...

Senior Project Manager

San Diego, CA · On-site

$88K - $115K/yr

Oversee the project management activities, including addressing clients' inquiries, preparing ... Strong understanding of drug discovery and development processes, particularly in preclinical ...

Senior Project Manager

San Diego, CA · On-site

$88K - $115K/yr

Oversee the project management activities, including addressing clients' inquiries, preparing ... Strong understanding of drug discovery and development processes, particularly in preclinical ...

The Project Manager will serve as an advisor and action officer for a science and technology ... preclinical development expertise to review proposals, technical reports, experimental or ...

Technical Project Manager

Emeryville, CA · On-site

$140K - $175K/yr

We're looking for a Technical Project Manager with experience in leadership/management of ... Full cell line development and preclinical scale up of customer molecules integrated into our ...

Showing results 41-60

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 Sep 11, 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.

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.
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Cities with the most Preclinical Project Manager job openings:

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Infographic showing various Preclinical Project Manager job openings in the United States as of September 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $102,682 per year, or $49.4 per hour.

Business Development, Preclinical/Clinical Solutions Senior Manager - West Coast

Remote

Azenta
1 - 5K employees

$150K/yr

Full-time

Posted 22 days ago


Azenta Life Sciences rating

7.5

Company rating: 7.5 out of 10

Based on 5 frontline employees who took The Breakroom Quiz


Job description

Azenta Inc.At Azenta, new ideas, new technologies and new ways of thinking are driving our future. Our customer focused culture encourages employees to embrace innovation and challenge the status quo with novel thinking and collaborative work relationships.
All we accomplish is grounded in our core values of Customer Focus, Achievement, Accountability, Teamwork, Employee Value and IntegrityJob TitleBusiness Development, Preclinical/Clinical Solutions Senior Manager - West CoastJob Description
Position Title: Business Development, Preclinical/Clinical Solutions Senior Manager

Location: Remote - US (West Coast)

Salary: $150,000 base + $70,000 SIP

Intro

Company Overview

At GENEWIZ by Azenta, new ideas, new technologies and new ways of thinking are driving our future. Our customer-focused culture encourages employees to embrace innovation and challenge the status quo with novel thinking and collaborative work relationships.

As a global leader in R&D genomics services, GENEWIZ, leads the way in providing superior data quality with unparalleled technical support to enable researchers around the world to advance their scientific discoveries faster than ever before.

Our customers at top-tier pharmaceutical, biotechnology, and academic institutions, as well as cutting-edge start-ups, rely on our proprietary technologies for consistent, reliable, high-quality data, even on the most difficult projects. A full-service provider, we provides Sanger DNA sequencing, gene synthesis, molecular biology, high throughput/next generation sequencing, bioinformatics, and GLP regulatory services

How You Will Add Value

The Business Development Preclinical/Clinical Solutions Senior Manager will be responsible for all US Preclinical and Clinical Solutions business and activities, including but not limited to expansion strategy, negotiation, and scoping future investment opportunities. The position incumbent will have full autonomy to target specific customer segments to accelerate new customer adoption.

What You Will Do

  • Serve as the primary driver for introducing the US Preclinical and Clinical Solutions portfolio to prospective clients. Own the end-to-end process-from pricing proposals and strategic planning to client engagement and successful project delivery.
  • Business Development Strategy: Develop and implement business development strategies to grow the preclinical and clinical services division, identifying new opportunities and markets for growth.
  • Client Acquisition and Relationship Management: Identify, pursue, and secure new business opportunities by building and maintaining strong relationships with key decision-makers in biotech, pharmaceutical, and CRO.
  • Sales Targets and Revenue Growth: Achieve revenue and business development targets by expanding the client portfolio and building long-term partnerships.
  • Cross-Functional Collaboration: Work closely with internal teams (project management, marketing, scientific experts & account managers) to ensure alignment of client needs with service offerings, and ensure the successful delivery of projects.
  • Market Analysis: Conduct competitive analysis and market research to identify trends, emerging opportunities, and potential clients in the preclinical and clinical space.
  • Contract Negotiation: Lead contract negotiations, ensuring favorable terms that align with company objectives while addressing client needs.
  • Customer Support: Deliver exceptional, high-level support to clients by ensuring their project requirements are met and addressing any concerns or challenges promptly to maintain strong and lasting relationships.
  • Attend Conferences and Networking Events: Represent the company at industry conferences, networking events, and trade shows to enhance brand visibility and attract new clients.

What you Will Bring

As this role involves consultative selling to Biotech/Pharma R&D teams and CMOs/CROs, a strong life sciences baseline is required to understand study designs, regulatory pathways, and translational science.

Education level:

  • Minimum requirement of a Bachelor's degree, with a PhD preferred.
  • Fields of Study: Life Sciences, Biology, Pharmacology, Biochemistry, Chemistry, Bioengineering

Work Experience:

  • Total Professional Experience: 7-10+ years in life sciences, pharmaceutical services, contract research organizations (CROs), or biotechnology environments.
  • Business Development: 5+ years of consultative sales, key account management, or commercial growth roles selling complex CRO/scientific solutions.

Domain Expertise:

  • Experience selling early-stage preclinical services AND/OR clinical solutions
  • Proven track record of managing long, consultative sales cycles (6-18 months) involving cross-functional technical teams and procurement departments.
  • Consistent history of meeting or exceeding annual quota metrics (typically $3M - $10M+ in annual contract value
  • Demonstrated capability in drafting, negotiating, and closing Master Services Agreements (MSAs), Statements of Work (SOWs)
  • An active network of decision-makers within regional biotech hubs, pharmaceutical companies, academic research institutes.

Working conditions

  • A fully Remote (Work from Home) position.
  • Frequent business travel (anticipated to be around 50%).
  • Must have a valid US driver's license

EOE M/F/Disabled/VET

If any applicant is unable to complete an application or respond to a job opening because of a disability, please email at Recruiting@azenta.com for assistance.

Azenta is an Equal Opportunity Employer. This company considers candidates regardless of race, color, age, religion, gender, sexual orientation, gender identity, national origin, disability or veteran status.

United States Base Compensation: $125,000.00 - $150,000.00

The posted pay range for this position is an estimate based on current market data and internal pay structure. Final compensation may vary above or below this range depending on factors such as experience, education (including licensure and certifications), qualifications, performance, and geographic location, among other relevant business or organizational needs.


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