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Project Manager Biotech Jobs in Vermont (NOW HIRING)

Amgen

Imaging Specialist Manager

Burlington, VT · On-site +1

It is key to our becoming one of the world's leading biotechnology companies. We are global ... Project and Program management and phenomenal communication skills * Degree educated THRIVE What ...

Amgen

Strategic Sourcing Manager

Burlington, VT · On-site

$129K - $167K/yr

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Project Management Experience - able to lead teams that cut across geographic and functional ...

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Project Manager Biotech information

See Vermont salary details

$23

$49

$81

How much do project manager biotech jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for project manager biotech in Vermont is $49.17, according to ZipRecruiter salary data. Most workers in this role earn between $42.69 and $53.94 per hour, depending on experience, location, and employer.

What does a project manager in biotech do?

A Project Manager in Biotech is responsible for planning, coordinating, and overseeing projects within biotechnology companies or research organizations. They work closely with scientists, regulatory teams, and other stakeholders to ensure that projects meet deadlines, stay within budget, and comply with industry regulations. Their tasks may include setting project timelines, managing resources, mitigating risks, and communicating progress to leadership. Project Managers play a crucial role in bringing new biotech products or research initiatives from conception to completion.

What are the key skills and qualifications needed to thrive as a project manager in biotech?

To thrive as a Project Manager in Biotech, you need a solid background in life sciences or engineering, experience in project management, and often a relevant degree such as a BSc or MSc, sometimes complemented by a PMP certification. Familiarity with project management software (such as MS Project or Jira), regulatory compliance systems, and budgeting tools is frequently required. Strong leadership, problem-solving, and effective communication skills set standout candidates apart by enabling them to coordinate cross-functional teams and manage complex timelines. These skills are essential to ensure that projects meet regulatory standards, stay on schedule, and achieve scientific and business goals.

How does a project manager in biotech typically collaborate with cross-functional teams to drive project success?

A Project Manager in the biotech sector routinely works with cross-functional teams that include scientists, regulatory experts, manufacturing staff, and quality assurance professionals. They coordinate meetings, align project timelines, and ensure clear communication of goals and milestones. Effective collaboration involves resolving conflicts, facilitating information flow among departments, and adapting plans as scientific or regulatory requirements evolve. This collaborative approach is essential for keeping projects on track, maintaining compliance, and achieving successful outcomes in a highly regulated and fast-paced industry.

What is the difference between Project Manager Biotech vs Clinical Project Manager?

AspectProject Manager BiotechClinical Project Manager
CredentialsBachelor's or Master's in Life Sciences, Project Management CertificationBachelor's or Master's in Life Sciences, Clinical Research Certification
Work EnvironmentBiotech companies, R&D labs, manufacturingClinical trial sites, hospitals, pharmaceutical companies
Industry UsageBiotech product development, research projectsClinical trial management, regulatory compliance
Common Search/ComparisonYesYes

The main difference between a Project Manager Biotech and a Clinical Project Manager lies in their focus areas. The Project Manager Biotech oversees research and development projects within biotech companies, focusing on product development and manufacturing. In contrast, the Clinical Project Manager specializes in managing clinical trials, ensuring regulatory compliance and patient safety. Both roles require strong project management skills and relevant certifications, but they operate in different phases of the biotech and pharmaceutical industry.

What are popular job titles related to Project Manager Biotech jobs in Vermont?

For Project Manager Biotech jobs in Vermont, the most frequently searched job titles are:

What job categories do people searching Project Manager Biotech jobs in Vermont look for?

The top searched job categories for Project Manager Biotech jobs in Vermont are:

Project Manager Biotech jobs near you
Infographic showing various Project Manager Biotech job openings in Vermont as of August 2026, with employment types broken down into 84% Full Time, 15% Part Time, and 1% Contract. Highlights an 79% Physical, 3% Hybrid, and 18% Remote job distribution, with an average salary of $102,268 per year, or $49.2 per hour.

Imaging Specialist Manager

Amgen

Burlington, VT • On-site, Remote

Full-time

Posted 13 days ago

Key responsibilities

  • Plan and execute imaging operations for clinical trials globally.

  • Manage and coordinate the operational imaging strategy, including planning, risk assessment, mitigation, and execution for clinical trials.

  • Provide oversight and expertise for imaging setup, startup activities, and maintain the quality and scientific integrity of imaging-related elements in clinical trials.

Job description

Career CategoryClinicalJob Description

HOW MIGHT YOU DEFY IMAGINATION?

If you feel likeyou'repart of something bigger,it'sbecause you are. AtAmgenour shared mission-to serve patients-drives all that we do. It is key to our becoming one of the world's leading biotechnology companies. We are global collaborators who achieve together-researching,manufacturingand delivering ever-better products that reachover10 million patientsworldwide.It'stime for a career you can be proud of. Join us.

IMAGING SPECIALIST MANAGER

LIVE

What you will do

In this vital role you will plan and execute imaging operations for clinical trials globally. You will manage and coordinate the operational imaging strategy, plan, risk assessment, mitigation, and execution for oncology and non-oncology clinical trials across all phases from study start-up to close-out.

Responsabilities:

  • Provide oversight and expertise for imaging setup and startup activities

  • Maintain the quality and scientific integrity of imaging-related elements in clinical trials

  • Working with the Imaging Scientist Team within Clinical Biomarkers & Diagnostics to enable E2E Imaging specialist support throughout the portfolio

  • Serve as an internal subject matter expert, advising Clinical Program Operations (CPO), and other Global Development Operations (GDO) functions, on best practices, ensuring consistent standards and key lessons learned are applied across the portfolio for continuous improvement and maximum impact of the solutions

  • Build global cross-functional relationships and collaborate with clinical teams to integrate imaging into trials and update senior management

WIN

What we expectofyou

We are all different, yet we all use our unique contributions to serve patients. What we seek in you as an experienced professional, are these qualifications and skills:

  • Experience in life sciences or medical fields, including imaging expertise and clinical research acquired working on clinical trials at a biotech, pharmaceutical or CRO company, having a strong understanding of clinical development programs in a global setting

  • Experience at or oversight of outside clinical research vendors (CRO's, central labs, imaging vendors, etc.)

  • Experience in operationalizing global clinical studies with imaging and vendor management

  • Good understanding of quality oversight and process improvement

  • Ability to network and establish relationships cross-functionally

  • Project and Program management and phenomenal communication skills

  • Degree educated

THRIVE

What you can expect of us

As we work to develop treatments that take care of others, so we work to care for our teammates' professional and personal growth and well-being.

  • Vast opportunities to learn and move up and across our global organization

  • Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act

  • Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Location: Ability to work remotely from UK/US.

APPLY NOW

for a career that defies imagination

In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us.

careers.amgen.com

Equal Opportunity Statement

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.

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