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Preclinical Development Jobs (NOW HIRING)

Administrative Ass3

Durham, NC · On-site

$16.50 - $21.75/hr

This position will function within the Operations and Planning Unit of Corporate Preclinical Development and Toxicology (CPDT) and will support the conduct of nonclinical laboratory investigations of ...

Manager Preclinical Research

Irvine, CA

$49K - $50K/yr

The Manager of Preclinical Research will be involved in the strategic development and growth of the preclinical research required to fuel the Electrophysiology and Cardiac Imaging portfolio and ...

New

Manager Preclinical Research

Irvine, CA · On-site

$49K - $50K/yr

The Manager of Preclinical Research will be involved in the strategic development and growth of the preclinical research required to fuel the Electrophysiology and Cardiac Imaging portfolio and ...

New

Provides strategic medical guidance and leads the development of experimental oncology agents in the TCO portfolio, beginning with PE / DC (Portfolio Entry / Drug Candidate) of preclinical ...

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Preclinical Development information

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$33K

$85K

$129K

How much do preclinical development jobs pay per year?

As of Jul 19, 2026, the average yearly pay for preclinical development in the United States is $85,045.00, according to ZipRecruiter salary data. Most workers in this role earn between $76,000.00 and $90,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Preclinical Development position, and why are they important?

To excel in Preclinical Development, you need a solid background in biology, pharmacology, or related life science fields, often supported by an advanced degree and experience with laboratory research. Familiarity with Good Laboratory Practice (GLP) regulations, data analysis software, and animal study management systems is expected. Strong attention to detail, effective problem-solving skills, and the ability to communicate complex findings clearly are valuable soft skills. These competencies are essential to ensure the successful and compliant progression of drug candidates toward clinical trials.

What is a Preclinical Development job?

A Preclinical Development job involves overseeing the research and testing of drug candidates before they enter clinical trials. Professionals in this role design and conduct studies to assess a drug’s safety, efficacy, and pharmacokinetics using laboratory and animal models. They collaborate with scientists, regulatory experts, and project managers to generate data required for regulatory approval. Their work helps identify potential risks and optimize drug formulations before human testing begins.

What are the typical responsibilities of someone working in Preclinical Development?

Professionals in Preclinical Development are responsible for designing, conducting, and analyzing laboratory and animal studies to evaluate the safety and efficacy of new drug candidates before clinical trials. They often collaborate closely with research scientists, regulatory teams, and project managers to ensure studies meet compliance standards and scientific objectives. Daily tasks may include developing protocols, interpreting data, preparing regulatory documentation, and troubleshooting experimental issues. This role offers opportunities to gain broad exposure to the drug discovery process and can lead to advancement into project leadership or regulatory affairs positions.

More about Preclinical Development jobs
What cities are hiring for Preclinical Development jobs? Cities with the most Preclinical Development job openings:
What are the most commonly searched types of Preclinical Development jobs? The most popular types of Preclinical Development jobs are:
What states have the most Preclinical Development jobs? States with the most job openings for Preclinical Development jobs include:
Infographic showing various Preclinical Development job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, and 2% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $85,045 per year, or $40.9 per hour.
Manager, R&D Operations

Manager, R&D Operations

Amylyx Pharmaceuticals

Cambridge, MA • On-site, Remote

Other

Posted 26 days ago


Job description

The Opportunity

We are seeking an R&D Operations Manager to lead operational planning and execution across our preclinical research and development organization. This role serves as a key business partner to scientific leadership, enabling efficient execution of toxicology, bioanalytical, translational, and research activities through strong operational oversight, vendor management, financial planning, and process optimization.

The R&D Operations Manager will be responsible for driving operational excellence across a growing preclinical organization, ensuring studies, vendors, budgets, contracts, and critical deliverables are managed proactively and efficiently. This position offers broad visibility across R&D and significant interaction with scientific leaders, external CROs, Finance, Procurement, Legal, and Quality.

Responsibilities

Operational Leadership

  • Support  operational planning and execution activities supporting preclinical, toxicology, bioanalytical, and translational research programs.
  • Partner with scientific leadership to develop and maintain integrated study plans, timelines, milestones, and operational deliverables.
  • Support identification of operational risks, develop and maintain program level risk tracker, and proactively work with scientific teams to develop mitigation strategies to support successful study execution.
  • Establish, implement, and continuously improve operational processes, tools, templates, and governance frameworks that increase organizational efficiency and scalability.
  • Support the Department Head with scheduling and executive assistant-based activities with approximate 15% time allocation.

Vendor and CRO Management

  • Serve as the primary operational lead for CROs, laboratories, consultants, and other external vendors supporting preclinical programs.
  • Manage vendor onboarding, contract initiation, statements of work, purchase orders, amendments, and vendor performance tracking.
  • Partner closely with Procurement, Legal, Finance, and Quality to ensure timely execution of agreements and vendor-related activities.
  • Monitor vendor deliverables, timelines, and budget performance, escalating issues as needed.

Study and Portfolio Operations

  • Facilitate department-level and cross-functional meetings, lead meeting notes and tracking of decisions, action items, and deliverables with clear documentation and tracking to completion.
  • Maintain operational oversight of study documentation, ensuring protocols, reports, contracts, and associated records are inspection-ready and appropriately archived.

Financial and Resource Management

  • Manage operational budgets for preclinical and toxicology activities, including purchase order management, invoice reconciliation, accrual tracking, and spend forecasting in partnership with the department head.
  • Partner with Finance to support annual budget planning and quarterly forecasting activities.
  • Develop reporting and dashboards that provide visibility into program level and study level costs, vendor spend, and resource utilization.

Continuous Improvement

    • Develop metrics and key performance indicators to measure operational effectiveness across preclinical programs.
    • Identify opportunities to streamline workflows, reduce cycle times, and improve collaboration across internal and external stakeholders.
    • Champion a culture of operational excellence, accountability, and continuous improvement.

Required Qualifications

  • Bachelor's degree in Life Sciences, Business, Operations, or a related field.
  • 6+ years of experience in biotechnology, pharmaceutical, CRO, or life sciences environments.
  • 3+ years of experience supporting preclinical development, toxicology, translational research.
  • Demonstrated experience managing vendors, CROs, contracts, budgets, and operational processes.
  • Experience partnering cross-functionally with scientific, finance, procurement, legal, and quality organizations.
  • Strong project management and organizational skills with the ability to manage multiple complex priorities simultaneously.
  • Excellent written and verbal communication skills and the ability to influence stakeholders across all levels of the organization.
  • Proficiency with Microsoft Office and common business systems; experience with NetSuite, LinkSquares, Smartsheet, or project management platforms is preferred.

Work Location and Conditions

  • At Amylyx, we proudly support remote work opportunities within the United States. However, due to business considerations related to health insurance coverage and state tax regulations, we are unable to hire employees who reside and/or work in certain states. Currently, we are not considering applicants from Alaska, Arizona, Hawaii Michigan and Tennessee.
  • You will be expected to travel to our corporate location in Cambridge, MA several times a year and attend other company-related events as necessary and requested.
  • You must have access to work in setting which enables meeting all requirements of the role (including privacy, reliable internet access, phone, ability to video conference, etc.) at your remote location.