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Project Manager Biotech Jobs in Melbourne, FL (NOW HIRING)

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Project Manager Biotech information

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$20

$42

$70

How much do project manager biotech jobs pay per hour?

As of Aug 28, 2026, the average hourly pay for project manager biotech in Melbourne, FL is $42.86, according to ZipRecruiter salary data. Most workers in this role earn between $37.21 and $47.02 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 Melbourne, FL?

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

What job categories do people searching Project Manager Biotech jobs in Melbourne, FL look for?

The top searched job categories for Project Manager Biotech jobs in Melbourne, FL are:

What cities near Melbourne, FL are hiring for Project Manager Biotech jobs?

Cities near Melbourne, FL with the most Project Manager Biotech job openings:

Project Manager Biotech jobs near you
Infographic showing various Project Manager Biotech job openings in Melbourne, FL as of July 2026, with employment types broken down into 1% As Needed, 91% Full Time, 1% Part Time, 1% Temporary, 5% Contract, and 1% Summer. Highlights an 82% Physical, 2% Hybrid, and 16% Remote job distribution, with an average salary of $89,155 per year, or $42.9 per hour.

Senior Scientist

National Strategic Research Institute

Melbourne, FL • On-site

$125K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 15 days ago

Job description

Job Title
Senior Scientist
Salary Minimum
$125K
Supervisor
Director of Biotechnology
Position Summary
The National Strategic Research Institute (NSRI) at the University of Nebraska is seeking applications for a Senior Scientist position that will encompass executing technical scientific approaches, development of business opportunities, leading technical tasks and identification of resources that support Department of War and other U.S. Interagency sponsors. The Senior Scientist will be responsible for providing support to several research programs over a capability area centered on biological threat detection and countermeasure development for Department of War (DoW) and United States Government (USG) sponsors. The Senior Scientist will work in a laboratory alongside a multidisciplinary team that develops, tests, and investigates novel materials, methods, and systems for chemical and biological defense applications in both field and laboratory settings. Additionally, the candidate will provide next generation sequencing (NGS) subject matter expertise, mentor junior staff, and draft experimental test plans. Ultimately, the candidate will be responsible for the development and enhancements of all aspects of NGS and forensic level analysis supporting Countering Weapons of Mass Destruction (CWMD) projects, while directly collaborating with NSRI staff and other entities within the CWMD community.
The primary place of duty for this position is NSRI’s facility in Melbourne, Florida. Secondary places of duty and travel requirements will be based on contractual, and project needs and may include NSRI facilities in Fredericksburg, Virginia; Annapolis Junction, Maryland; along with USG facilities as required by contract requirements. Periodical travel to Omaha, Nebraska and University of Nebraska facilities and campuses in Nebraska is also anticipated.
This position is part of a government-funded project, and employment is contingent upon continued customer funding and performance.
Priority Consideration: In alignment with our commitment to staff development and internal mobility, current NSRI employees will be given priority consideration for this vacancy, provided they meet the minimum qualifications. Internal candidates are strongly encouraged to apply.
Duties and Responsibilities
  • Provide technical contributions as a Senior Scientist regarding all aspects of government programs to include design/development, optimization, and execution of sample preparation, real-time PCR, ddPCR, CRISPR, NGS methodologies and bioinformatics to accomplish all stated and implied project related tasks.
  • Develop biological defense research, development, and testing capabilities at both NSRI and partner facilities to aid in the building of long-term strategic resources and the facilitation of immediate project needs.
  • Collaborate directly with project sponsors, stakeholders, University of Nebraska staff, and NSRI staff to develop and execute project plans, timelines, and strategies to facilitate successful completion of project goals.
  • Act as Principal Investigator, execute, and defend the cost, scope, technical performance, and schedule for assigned projects.
  • Provide project deliverables to report project status, written and orally, both internally and externally
  • Implement and manage change when necessary to meet project outputs
  • Execute and manage day-to-day laboratory duties associated with assigned projects
  • Lead and/or contribute to multiple projects simultaneously
Minimum Qualifications
  • Bachelor's degree in Biotechnology, Biology, Microbiology, or Molecular Biology from an accredited university or college
  • 8+ years technical experience working in support of DoW, USG or related projects
  • 8+ years’ experience in RT-PCR, ddPCR, NGS methodologies, CRISPR and creating protocols and conducting experiments in a laboratory environment
  • 8+ years’ experience NGS workflows including agnostic whole genome sequencing, amplicon sequencing, transcriptome characterization as well as various pre-processing methods
  • Knowledge of bioinformatics analysis (CLC Genomics Workbench and various Illumina BaseSpace apps) principles and its application for next-generation sequencing genomic data analysis
  • Experience with BSL-3 procedures including sequencing in high containment laboratories
  • Excellent written and oral skills
  • Excellent organizational and time management skills
  • Experience working as a part of a multi-functional team
  • U.S. citizenship and the ability to obtain and maintain a U.S. government security clearance, with options for higher level clearance opportunities.
Desired Qualifications
  • Master’s Degree or PhD preferred in biotechnology, microbiology, biochemistry or molecular biology, or related field.
  • 10+ years technical experience working in support of DoW, USG or related projects
  • 10+ years’ experience in RT-PCR, ddPCR, NGS methodologies, CRISPR and creating protocols and conducting experiments in a laboratory environment
  • 10+ years’ experience NGS workflows including agnostic whole genome sequencing, amplicon sequencing, transcriptome characterization as well as various pre-processing methods
  • 2+ years of experience working in remote OCONUS (Outside Continental U.S.) based laboratories.
  • 5+ years of experience developing human signature capability.
  • Experience in performing as a Principal Investigator for CDC select agent programs
  • American Society for Clinical Pathology certified Medical Technology in molecular Biology
  • Active U.S. government security clearance
Benefits
  • Health
  • Dental
  • Vision
  • ER-paid Life
  • Vol Life (employee, spouse, child(ren))
  • AD amp;D
  • LTD
  • 403b (retirement), with employer matching
  • Paid time off
  • Paid holidays

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