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Biotechnology Project Manager Jobs in Raleigh, NC

Project Managers own the operational strategy, determining the most cost effective and efficient ... Experience working with Biotech clients * In lieu of the above requirement, candidates with (a) six ...

Project Managers own the operational strategy, determining the most cost effective and efficient ... Experience working with Biotech clients * In lieu of the above requirement, candidates with (a) six ...

Land Development Project Manager

Raleigh, NC · Hybrid

$89K - $115K/yr

Our clients include mixed-use, biotech, residential, multifamily, affordable housing, industrial ... Direct projects by managing and delegating tasks, forecasting and proactively addressing workload ...

Land Development Project Manager

Raleigh, NC · On-site

$89K - $115K/yr

Our clients include mixed-use, biotech, residential, multifamily, affordable housing, industrial ... Direct projects by managing and delegating tasks, forecasting and proactively addressing workload ...

Land Development Project Manager

Raleigh, NC · Hybrid

$89K - $115K/yr

Our clients include mixed-use, biotech, residential, multifamily, affordable housing, industrial ... Direct projects by managing and delegating tasks, forecasting and proactively addressing workload ...

Land Development Project Manager

Raleigh, NC · On-site

$88K - $114K/yr

Land Development Project Manager Job Locations US-NC-Raleigh ID 2026-6075 Category Engineering Type ... Our clients include mixed-use, biotech, residential, multifamily, affordable housing, industrial ...

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Biotechnology Project Manager information

See Raleigh, NC salary details

$21

$44

$74

How much do biotechnology project manager jobs pay per hour?

As of Jul 14, 2026, the average hourly pay for biotechnology project manager in Raleigh, NC is $44.95, according to ZipRecruiter salary data. Most workers in this role earn between $39.04 and $49.33 per hour, depending on experience, location, and employer.

What does a Biotechnology Project Manager do?

A Biotechnology Project Manager oversees and coordinates projects within the biotechnology industry, ensuring that research and development initiatives, product launches, or clinical trials are completed on time and within budget. They work with cross-functional teams, including scientists, engineers, and regulatory experts, to set project goals, manage resources, and monitor progress. Their responsibilities also include risk management, stakeholder communication, and ensuring compliance with industry regulations. This role is vital for driving innovation and bringing new biotech products or solutions to market efficiently.

What is the difference between Biotechnology Project Manager vs Research Scientist?

AspectBiotechnology Project ManagerResearch Scientist
Required CredentialsBachelor's or Master's in Biotechnology, Project Management certification often preferredMaster's or PhD in Biotechnology or related field
Work EnvironmentProject teams, corporate labs, industry settingsResearch labs, academic institutions, industry research divisions
Employer & Industry UsageBiotech companies, pharmaceutical firms, biotech startupsUniversities, research institutes, biotech companies

The main difference is that a Biotechnology Project Manager oversees project planning, coordination, and execution within biotech companies, focusing on timelines and budgets. In contrast, a Research Scientist conducts experiments and develops new biotech products or knowledge. Both roles require strong biotech credentials, but their daily tasks and focus areas differ significantly.

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

To thrive as a Biotechnology Project Manager, you need a solid background in biological sciences or engineering, project management expertise, and often an advanced degree such as an MSc or PhD. Familiarity with tools like Microsoft Project, Gantt charts, regulatory compliance systems, and certifications such as PMP are commonly required. Strong leadership, communication, and problem-solving skills set exceptional candidates apart in managing cross-functional teams and complex timelines. These skills and qualities are essential to effectively coordinate scientific projects, ensure regulatory compliance, and deliver successful outcomes in a dynamic biotech environment.

What are some common challenges faced by Biotechnology Project Managers in cross-functional team environments?

Biotechnology Project Managers often work with multidisciplinary teams composed of scientists, regulatory specialists, manufacturing experts, and business development professionals. One common challenge is ensuring clear communication and alignment across these diverse groups, especially when technical jargon or differing priorities create misunderstandings. Additionally, managing project timelines in a highly regulated environment, where unexpected trial results or compliance issues may cause delays, requires strong adaptive planning. Successful Biotechnology Project Managers foster collaboration by setting clear goals, conducting regular check-ins, and proactively addressing potential roadblocks.
What are popular job titles related to Biotechnology Project Manager jobs in Raleigh, NC? For Biotechnology Project Manager jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Biotechnology Project Manager jobs in Raleigh, NC look for? The top searched job categories for Biotechnology Project Manager jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Biotechnology Project Manager jobs? Cities near Raleigh, NC with the most Biotechnology Project Manager job openings:
Infographic showing various Biotechnology Project Manager job openings in Raleigh, NC as of July 2026, with employment types broken down into 81% Full Time, 3% Part Time, 3% Temporary, and 13% Contract. Highlights an 94% In-person, 3% Hybrid, and 3% Remote job distribution, with an average salary of $93,499 per year, or $45 per hour.
Clinical Project Manager II

Clinical Project Manager II

Fortrea

Durham, NC

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 28 days ago


Fortrea rating

7.2

Company rating: 7.2 out of 10

Based on 9 frontline employees who took The Breakroom Quiz

47th of 59 rated research


Job description

Our FSO team is seeking an Cell & Gene Therapy Clinical Project Manager to join our growing team. This role requires 2+ years of global project management experience, with experience in cell & gene therapy. Candidates must be based in the United States.

Job Overview:

Project Managers own the operational strategy, determining the most cost effective and efficient means to successfully run and complete projects on time, while maintaining quality, remaining within budget, while meeting the customer's needs and adhering to the contract. Project Managers will work to develop and lead high performing teams by collaborating with key stakeholders to manage all aspects of the end-to-end lifecycle of the project including scope, timelines, risk, and budget. A successful Project Manager will bring innovation and future focused approaches to clinical trials with a focus on patient centricity and consistent solutions-oriented delivery.

    Summary of Responsibilities:

    • Take accountability for proactively driving project performance toward contracted deliverables while meeting customer needs and maintaining operational excellence.
    • Take ownership of the customer relationship while drawing on the Company's pool of experts.
    • Drive communication and collaboration with the client and project team across a matrixed, multi-cultural, environment. Lead the development of the project strategy and ensure prioritization with the project team and key stakeholders in the creation of clear, data driven strategies and proactive management of project scope, timelines, quality, and budget. In collaboration with relevant departments, prepare and deliver presentations for new business as required.
    • Lead the identification of project, financial and quality risk leveraging end to end risk management practices and quality by design principles. Appropriately utilize data sources, dashboards, and risk management strategies to drive innovation and proactive problem solving with the project and client teams. Lead the adherence to project governance and issue escalation pathways, ensuring that project plans are in place to address identified risk while adhering to professional standards, SOPs, client, and regulatory requirements.
    • Partner with project team members and key stakeholders to oversee and manage project budgets, resources, and scope. Ensure adherence to established budget and financial milestones. Accountable for accurately forecasting project revenue and managing project costs in adherence to the budget. Leading the timely management of changes to scope and the change order process. Ensures project team awareness and tracking of KPIs for any client specific metrics.
    • Provide inspiring leadership and play a key role in the creation of high performing project teams. Facilitating communication and teamwork while driving delivery, ensuring that team members understand contracted scope, timelines, and budget. Ensures that resource projections are accurate and visible to resourcing teams, proactively escalating resource constraints and challenges. Develops and mentors team members in multiple areas of expertise and provides feedback as needed to respective line managers.
    • All other duties as needed or assigned.

    Qualifications (Minimum Required):

    • University/college degree (life science preferred) or certification in a related allied health profession (i.e., nursing, medical or laboratory technology) from an appropriately accredited institution.
    • Fortrea may consider relevant and equivalent experience in lieu of educational requirements.

    Experience (Minimum Required):

    • Minimum of five (5) years of relevant clinical research experience in a pharmaceutical company/CRO.
    • 2+ years of Clinical Project Management experience within a CRO or pharma company
    • Experience working on Cell & Gene Therapy studies
    • Experience working with Biotech clients
    • In lieu of the above requirement, candidates with (a) six (6) years supervisory experience in a heath care setting and (b) five (5) years clinical research experience including one (1) years of project management experience (international clinical trial management experience preferred) in the pharmaceutical or CRO industries will be considered
    • Working knowledge of ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs.
    • Advanced computer skills (e.g., Microsoft Word, Excel, Project, Access, and Power Point).
    • Experience managing projects in a matrix and virtual environment.
    • Excellent communication, planning, and organizational skills.
    • Demonstrated ability to lead by example and to encourage team members to seek solutions independently.
    • Demonstrated ability to handle multiple competing priorities and to utilize resources effectively.
    • Demonstrated ability to inspire effective teamwork and motivate staff within a matrix system.
    • Financial awareness and ability to actively utilize financial tracking systems.
    • Ability to work independently and mentor junior project team members.
    • Ability to negotiate and liaise with clients in a professional manner.
    • Ability to present to staff at all levels.

    Preferred Qualifications Include:

    • Master's or other advanced degree.
    • PMP certification

    What do you get?

    Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including but not limited to:

    • Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers)

    • 401(K)

    • Paid time off (PTO) - Flex Plan

    • Employee recognition awards

    • Multiple ERG's (employee resource groups)

    • Target Pay Range (based on title): $ 125 - 135k

    #LI - Remote

    Applications will be accepted on an ongoing basis

    Physical Demands/Work Environment:

    • Standard Office Environment or remote based work required.
    • Weekend and off-hour work as required.

    Travel Requirements:

    • Local, Domestic, Regional, Global

    Identify the expected travel requirements of the position on an annual basis:

    • % of time: up to 30%
    • % of the above that requires overnight stay: up to 30%
    • Travel is primarily to where: domestic and international travel

    Learn more about our EEO & Accommodations request here.


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