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Project Manager Biotech Jobs in Delaware (NOW HIRING)

This critical role provides project management from the first point of contact with R&D through ... Biotechnology, Biochemistry, or related field with at least eight (8) years of relevant post ...

Pharmacovigilance Safety Manager

Newark, DE ยท On-site

$100K - $130K/yr

QPS' Story Since its inception, QPS has been assisting pharmaceutical, biotechnology, and medical ... Serve as the primary safety contact for sponsors, clinical project managers, the QPS Safety Team ...

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Project Manager Biotech information

See Delaware salary details

$21

$46

$76

How much do project manager biotech jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for project manager biotech in Delaware is $46.28, according to ZipRecruiter salary data. Most workers in this role earn between $40.19 and $50.77 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 Delaware?

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

What cities in Delaware are hiring for Project Manager Biotech jobs?

Cities in Delaware with the most Project Manager Biotech job openings:

Infographic showing various Project Manager Biotech job openings in Delaware as of August 2026, with employment types broken down into 85% Full Time, 13% Part Time, and 2% Contract. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $96,267 per year, or $46.3 per hour.

Infrastructure & Capital Projects - Lab Construction Manager, ANS

Accenture Infrastructure and Capital Projects, LLC

Wilmington, DE โ€ข On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 3 days ago

New


Job description

You've Never Been Satisfied with "Good Enough."
You want to make an impact, not just manage projects, but change how the world gets built. At Accenture Infrastructure & Capital Projects, you'll do exactly that. You'll help develop and deliver the factories, grids, transit systems, and public infrastructure that keep communities moving - and do it smarter, safer, and more sustainably than ever before.
You'll work alongside people who think big and act bold - project managers, engineers, technologists, and strategists who blend real-world experience with digital innovation and AI. Together, we're transforming how capital projects are planned, managed, and executed, creating a better way to build for the future.
Because "good enough" builds the past. You're here to build what's next, on a team that outperforms every norm.
Visit us here to learn more about Accenture Infrastructure & Capital Projects
As Accenture continues to grow, you may see a variety of new career opportunities, and depending on the role and location you may be directed to apply through Accenture Infrastructure and Capital Projects LLP or one of our other legal entities - Accenture Infrastructure and Capital Projects, LLC or Accenture Infrastructure and Capital Projects Inc., with benefits varying by country and role, so please check with your recruiter for details.
THE WORK:
  • You'll lead construction and renovation projects for QC laboratories, pharmaceutical and biotechnology facilities, cleanrooms, manufacturing support areas, and other regulated life sciences environments.
  • You'll manage field execution from project planning through turnover, ensuring alignment with scope, schedule, budget, quality standards, safety requirements, and client expectations.
  • You'll coordinate daily construction activities with engineering, quality, validation, commissioning, EHS, operations teams, contractors, vendors, and client stakeholders.
  • You'll oversee contractor performance, field resources, construction sequencing, and site logistics to support efficient project delivery in active facilities.
  • You'll facilitate site walk-downs, coordination meetings, readiness reviews, safety audits, job briefings, and contractor alignment discussions to maintain accountability and communication.
  • You'll support construction activities in GMP and non-GMP environments while minimizing operational disruptions and maintaining contamination control and facility access requirements.
  • You'll apply technical knowledge of MEP systems, HVAC controls, electrical systems, clean utilities, laboratory gases, pressure cascades, HEPA filtration, laboratory equipment installations, and cleanroom infrastructure.
  • You'll identify and mitigate project risks, resolve field issues, develop recovery strategies, evaluate budget impacts, and provide accurate project status updates.
  • You'll coordinate commissioning, qualification, and validation readiness activities, including field verification, punch list management, documentation turnover, vendor coordination, and system startup support.
  • You'll foster a culture of safety, quality, compliance, teamwork, and continuous improvement while building strong relationships with clients, contractors, and project partners.
  • Flexible: The work location for this role will include a mix of working remotely, onsite at a client or in an Accenture office or center.

HERE'S WHAT YOU'LL NEED:
  • Bachelor's degree in Engineering, Construction Management, or a related discipline; alternatively, a high school diploma/GED with equivalent construction management experience.
  • Minimum 10 years of construction management experience, including experience supporting regulated life sciences, pharmaceutical, biotechnology, laboratory, cleanroom, or manufacturing facilities.
  • 10 years of experience managing multiple contractors, field teams, project priorities, budgets, schedules, and stakeholder expectations in complex construction environments.
  • Industry experience within pharmaceutical, biotechnology, life sciences, laboratory, cleanroom, GMP, or regulated manufacturing environments.
  • Technical knowledge of MEP systems, HVAC controls, electrical systems, clean utilities, laboratory gases, pressure cascades, HEPA filtration, laboratory equipment installation, commissioning support, and construction project execution.

BONUS POINTS IF YOU HAVE:
  • Direct experience delivering QC laboratories, analytical laboratories, microbiology laboratories, pharmaceutical laboratories, cleanrooms, or GMP facility construction projects.
  • OSHA 30 certification or willingness to obtain the certification.
  • Experience coordinating shutdowns, outages, tie-ins, phased construction, and work within occupied or operational laboratory and manufacturing facilities.
  • Strong understanding of OSHA regulations, Lockout/Tagout (LOTO), electrical safety requirements, job hazard analysis, and contractor safety management.
  • Familiarity with commissioning, qualification, validation processes, turnover documentation, quality systems, and inspection readiness requirements.

$140,000 - $170,000 a year
Compensation at Accenture varies depending on a wide array of factors, which may include but are not limited to the specific office location, role, skill set, and level of experience. As required by local law, Accenture provides a reasonable range of compensation for roles that may be hired in Illinois, Maine, Minnesota, California, Colorado, District of Columbia, Maryland, Massachusetts, New York, New Jersey, Ohio, Virginia or Washington as set forth below.
We believe that no one should be discriminated against because of their differences. All employment decisions shall be made without regard to age, race, creed, color, religion, sex, national origin, ancestry, disability status, veteran status, sexual orientation, gender identity or expression, genetic information, marital status, citizenship status or any other basis as protected by federal, state, or local law. Our rich diversity makes us more innovative, more competitive, and more creative, which helps us better serve our clients and our communities.
For details, view a copy of the Accenture Equal Opportunity and Affirmative Action Policy Statement
Accenture is an EEO and Affirmative Action Employer of Females/Minorities/Veterans/Individuals with Disabilities.
Accenture is committed to providing veteran employment opportunities to our service men and women.
Accenture I&CP offers a comprehensive benefits package including medical, dental, and vision coverage; basic life and AD&D insurance; short- and long-term disability; a 401(k) with employer match; health savings and flexible spending accounts; paid time off and holidays; paid maternity and parental caregiver leave; adoption and surrogacy assistance; supplemental insurance plans; an employee assistance program; legal resources; and identity theft protection.
Benefits eligibility may vary by state, country, and role. Please connect with your recruiter for more information.