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Project Manager Biotech Jobs in Gaithersburg, MD

Provide solutions and white papers to technology and project management. (in biotechnology, medical operations, DoD tactical networks, and aviation) * Propose and defend products to CDID through ...

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

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

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

... biotech, healthcare, commercial, transportation, and technology companies, as well as many ... Plan and organize a project under the directions of a Project Manager or Senior Project Manager

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Project Manager Biotech information

See Gaithersburg, MD salary details

$23

$49

$82

How much do project manager biotech jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for project manager biotech in Gaithersburg, MD is $49.96, according to ZipRecruiter salary data. Most workers in this role earn between $43.37 and $54.81 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 Gaithersburg, MD?

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

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

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

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

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

Infographic showing various Project Manager Biotech job openings in Gaithersburg, MD as of August 2026, with employment types broken down into 83% Full Time, 16% Part Time, and 1% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $103,922 per year, or $50 per hour.

Project Manager USAMMA

The Tauri Group

Frederick, MD โ€ข On-site

Contractor

Medical, Dental, Vision

Re-posted 10 days ago


Job description

Company Description
Established in 2001, The Tauri Group is a professional services firm known for our
analytic rigor, practical solutions, and trusted advice in the areas of CBRN
threat mitigation, defense science and technology, homeland security, and
adjacent domains. We offer the financial stability and breadth of capability of
a large company coupled with the corporate commitment and attention of a small
firm. Our subject matter expertise, determination, agility, and commitment to
active and ongoing client and stakeholder engagement enable us to solve tough
problems and deliver results-oriented solutions that help our customers achieve
mission success. We tackle our clients' most challenging problems by
combining analytical rigor with world-class expertise and relevant operational
experience. At The Tauri Group, we do what's right for the Program, the
Mission, and the Nation.
Job Description
We are seeking a Project Manager to support the US Army Medical Materiel Agency's (USAMMA) mission to develop, manage and perform end to end life cycle logistics on medical equipment to protect and sustain the Warfighter's and their families for the Nation.
Candidates must have a current minimum Public Trust clearance
Responsibilities
  • Build and develop a detailed an Integrated Master Schedule (IMS) in MS Project
  • Provide solutions and white papers to technology and project management. (in biotechnology, medical operations, DoD tactical networks, and aviation)
  • Propose and defend products to CDID through advanced development, production, and fielding meetings and discussions
  • Provide written technical opinions to guide the decision making process of the IPT, and lead project teams and participate in the evaluation of technical results in multiple developmental areas, developing strategies to move the program forward
  • Collaborate with both internal and external partners, contributing to data analyses in order to create and submit study results to publications or the FDA
  • Prepare documentation to include but not limited to market research, acquisition strategy, independent government cost estimate, performance work statement, purchase request, justification & approval on RDT&E Contracts
  • Assess cost, schedule, and performance risks and develop mitigation strategies with knowledge of DoD 5000.02 Acquisition Process, CJCSI 3170.01 JCIDS System, Financial Management Regulation, and the Federal Acquisition Regulation
  • Provide technical input, build slides, and draft documents to support to acquisition presentations and documentations in support of major milestones, program reviews, or other program presentations
  • Develop drafts and assist the project team to coordinate responsibilities, oversee quality management, and encourage timeliness of completion of protocols, other regulatory submissions, and technical, and acquisition reports
  • Prepare documentation/presentations to summarize technical results, to include displaying results in "Layman's" terms, formulating conclusions, and developing technical strategies in response to the data outcomes such as an After Action Review

Qualifications
Education and Experience Required
  • Public Trust Clearance: Desired: Secret
  • Bachelor's Degree in Engineering, Physics, Life Sciences or related discipline; Master's Degree in Engineering, Physics, Life Sciences or related discipline preferred
  • Minimum of eight (8) years general experience and six (6) years relevant experience
  • DoD Acquisition experience using DOD 5000.02 processes and requirements
  • Experience using Microsoft Project to develop and maintain resource loaded project schedules
  • Familiarity with work breakdown structures for task oriented RDT&E programs
  • Experience leading IPTs and other stakeholder engagements including technical discussions
  • Experience preparing and delivering documents ranging from technical reviews to acquisition documentation
  • Desired: experience with medical product development, test and evaluation, and regulatory approval processes
  • Desired Certifications: PMP, DAU Level II or higher

Additional Information
At The Tauri Group, you'll collaborate with an elite, creative team of scientists,
engineers, analysts, operations specialists, policy experts, and acquisition
support specialists. We attract people who love their work and are dedicated to
the complex challenges facing today's world. Our culture fosters engagement and
enthusiasm, attracts and retains proven experts, and maintains a flexible
environment that supports clients and staff.
We support your life outside of the office, too, with benefits including:
  • Highly competitive medical insurance and multiple plans to choose from
  • Dental and vision insurance plans
  • Tuition assistance
  • Professional development opportunities
  • Eight paid hours a year that you can devote to charity
  • Flexible work schedules

The Tauri Group is an EEO employer. To find out more about us, please visit our
website at www.taurigroup.com.