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Project Manager Biotech Jobs in Laurel, MD (NOW HIRING)

CRB

Project Coordinator II

Rockville, MD

The Project Coordinator II assists the Project Manager in delivery of small- to large-scale capital ... Experience in pharmaceutical, biotechnology, or advanced technology projects preferred

CRB

Project Coordinator II

Rockville, MD · On-site

The Project Coordinator II assists the Project Manager in delivery of small- to large-scale capital ... Experience in pharmaceutical, biotechnology, or advanced technology projects preferred

CRB

Project Coordinator II

Rockville, MD · On-site

The Project Coordinator II assists the Project Manager in delivery of small- to large-scale capital ... Experience in pharmaceutical, biotechnology, or advanced technology projects preferred

IQVIA

CRA 1, IQVIA Biotech

Rockville, MD

$71K - $145K/yr

The ability to manage multiple tasks, prioritize effectively, and work independently while ... Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...

IQVIA

CRA 1, IQVIA Biotech

Rockville, MD · On-site

$71K - $145K/yr

The ability to manage multiple tasks, prioritize effectively, and work independently while ... Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...

Jobtailor

Principal, Policy

Washington, DC · On-site

$120 - $180/hr

... by a biotech or health insurance company, relevant trade group, advocacy organization, Capitol Hill, the executive branch, or a professional advisory services firm * Prior project management ...

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Project Manager Biotech information

See Laurel, MD salary details

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How much do project manager biotech jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for project manager biotech in Laurel, MD is $45.85, according to ZipRecruiter salary data. Most workers in this role earn between $39.81 and $50.29 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 Laurel, MD?

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

What job categories do people searching Project Manager Biotech jobs in Laurel, MD look for?

The top searched job categories for Project Manager Biotech jobs in Laurel, MD are:

What cities near Laurel, MD are hiring for Project Manager Biotech jobs?

Cities near Laurel, MD with the most Project Manager Biotech job openings:

Project Manager Biotech jobs near you
Infographic showing various Project Manager Biotech job openings in Laurel, MD as of August 2026, with employment types broken down into 77% Full Time, 22% Part Time, and 1% Contract. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $95,363 per year, or $45.8 per hour.

Project Manager | Agile Scrum Master

Black Canyon Consulting

Bethesda, MD • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 11 days ago

Job description

Overview
Black Canyon Consulting (BCC) is actively looking for Project Manager/Agile Scrum Master to support our work for the National Center for Biotechnology Information (NCBI) at the National Library of Medicine (NLM), an institute of the National Institutes of Health. This opportunity is full time and onsite at the NIH-NCBI in Bethesda, MD and/or remote work.
NCBI is part of the National Library of Medicine (NLM) at NIH. NCBI is the world's premier biomedical center hosting over six million daily users that seek research, clinical, genetic, and other information that directly impacts biomedical research and public health - at NCBI you can literally help to accelerate cures for diseases! NCBI's wide range of applications, platforms (node, python, Django, C++, you name it) and environments (big data [petabytes], machine learning, multiple clouds) serve more users than almost any other US Government Agency according to https://analytics.usa.gov/.
We attract the best people in the business with our competitive benefits package that includes medical, dental and vision coverage, 401k plan with employer contribution, paid holidays, vacation, and tuition and conference reimbursement. If you enjoy being a part of a high performing, professional service and technology focused organization, please apply today!
Duties & Responsibilities:
  • Coordinates the full software development lifecycle (SDLC) in a scientific environment, including defining technical and functional requirements, quality control planning, implementation, upgrades, and integration with existing NCBI systems through Agile Process methodology.
  • Position includes daily coordination of complex technical projects dealing with scientific and genomic data.
  • Participate in and provide technical and administrative expertise to software development projects.
  • Responsible for software/system design and specifications, system implementation and integration, and testing.
  • Will be responsible for tracking milestones, and producing deliverables.
  • Balances risks, schedules, and resources.
  • Coordinates cross-functional teams of various sizes with diverse technical skills sets.
  • Advises senior management on technical issues.
  • Communicates project issues to stakeholders and senior management.
Required Skills:
  • Formal education (minimum: Bachelor's degree) in Computer Science or related field.
  • Requires at least 3 years of project management experience and at least 5 years of experience developing the software and/or managing the software development.
  • Strong Technical Knowledge of software application development.
  • Experience managing software development projects using Agile methodology
  • Experience coordinating work across multiple teams and departments.
  • Effective verbal and written communications.
  • Experience in delivery of complex enterprise level software development projects
Desired Skills:
  • Master's degree preferred.
  • PMP Certification
  • Experience with scientific or biological data a plus.
  • Experience as software development technical lead.
  • Experience working with large databases, statistical analysis, and clinical data.
  • Experience in a research and development (R&D) environment with demonstrated ability to analyze problems and propose multiple solutions.
  • Experience with large distributed systems and cloud computing.

Benefits and Salary
We attract the best people in the business with our competitive benefits package that includes medical, dental and vision coverage, 401k plan with employer contribution, paid holidays, vacation, and tuition reimbursement.
We offer a competitive salary commensurate with experience and location. The targeted range for this position is $125,000 - $150,000.
If you enjoy being a part of a high performing, professional service and technology focused organization, please apply today!

Apply