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Preclinical Project Manager Jobs in Florida (NOW HIRING)

UAB

RESEARCHER ASSOCIATE

Tampa, FL

This position requires independent judgment and technical expertise to support complex preclinical ... management skills to coordinate multiple concurrent research projects and deadlines. * Strong ...

TeamSoft

Research Principal Scientist

Jacksonville, FL · On-site

$100 - $111/hr

Hands-on experience with preclinical in vivo research, including large animal studies. * Experience supporting regulated medical device development. * Proven project management and cross-functional ...

Amaris Consulting

Research Scientist

Jacksonville, FL · On-site

... preclinical and technical data clearly and credibly to expert audiences, management, external ... Strong collaboration and negotiation skills related to project scope, study design, process ...

Aequor

Demonstrated ability to present preclinical and scientific data clearly, credibly, and persuasively ... Experience with successful project management is required.Experience supporting regulated product ...

Lancesoft

Research Scientist

Jacksonville, FL · On-site

$80 - $93.75/hr

Demonstrated ability to present preclinical and scientific data clearly, credibly, and persuasively ... Experience with successful project management is required. * Experience supporting regulated ...

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Preclinical Project Manager information

How does a Preclinical Project Manager typically coordinate with cross-functional teams during a drug development project?

A Preclinical Project Manager works closely with scientists, regulatory affairs, toxicology, and external vendors to ensure all preclinical studies are executed on time and within budget. They facilitate regular meetings to align project milestones, address challenges, and manage documentation for compliance. Effective communication and proactive issue resolution are key, as the role often requires balancing the needs of diverse stakeholders while keeping the overall project timeline on track.

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

To thrive as a Preclinical Project Manager, you need a solid background in life sciences or pharmaceutical research, often with an advanced degree and experience managing preclinical studies. Familiarity with project management tools, regulatory guidelines (such as GLP), and software like Microsoft Project or similar platforms is typically required. Strong organizational, leadership, and communication skills are vital for coordinating cross-functional teams and ensuring project timelines are met. These skills and qualifications are crucial for efficiently advancing drug candidates through preclinical development while ensuring compliance and project success.

What does a Preclinical Project Manager do?

A Preclinical Project Manager oversees the planning, coordination, and execution of preclinical research projects that typically involve laboratory and animal studies before clinical trials in humans can begin. They work closely with scientists, regulatory teams, and stakeholders to ensure that studies are conducted according to protocols, timelines, and regulatory requirements. Their responsibilities include managing budgets, resources, and communication among various teams to advance drug candidates or medical devices through the early stages of development. Effective Preclinical Project Managers help ensure that projects meet scientific and business objectives, and that all data generated is reliable and compliant with industry standards.
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Preclinical Project Manager jobs near you

Principal Scientist

Mainz Brady Group

Jacksonville, FL • On-site

Other

Posted 7 days ago

Job description

Principal Scientist – Neuroscience & Biological Safety


We are seeking a Principal Research Scientist to lead and support investigational and preclinical research for neuro-based stereotactic medical devices. This individual will guide research planning, laboratory and in vivo study execution, biological evaluation, risk assessment, and scientific documentation supporting product development and regulatory objectives.

The ideal candidate brings strong expertise in neuroscience, medical device biological safety, ISO 10993, and preclinical research. This role will serve as a scientific subject matter expert to R&D, Clinical Affairs, Regulatory Affairs, Quality, Marketing, and other cross-functional partners.

Key Responsibilities

  • Lead and support research involving neuro-oncology, neuro-endoscopy, neurosurgery, and other neuro technologies with stereotactic integration.
  • Develop and review study protocols, technical reports, biological evaluation documentation, and biological safety risk assessments.
  • Establish scientific strategies for technical investigations and neuro-specific product testing.
  • Conduct biocompatibility assessments and develop testing strategies in accordance with ISO 10993.
  • Coordinate laboratory and preclinical studies, including in vivo and large-animal research, while tracking outcomes and deliverables.
  • Develop biological safety content and scientific rationale for regulatory submissions.
  • Serve as a biological safety and neuroscience subject matter expert for new product development and sustaining products.
  • Present preclinical, scientific, and technical data to internal teams, external experts, key opinion leaders, and regulatory stakeholders.
  • Partner with laboratories, CROs, suppliers, surgeons, and external research organizations.
  • Provide scientific guidance to R&D, Regulatory Affairs, Clinical Affairs, Marketing, Sales, Quality, and manufacturing teams.
  • Support project planning, technical reviews, risk assessments, and cross-functional research initiatives.

Qualifications

  • Master’s degree in neuroscience, biomedical science, biology, toxicology, materials science, or a related scientific field required; PhD or DVM preferred.
  • Master’s degree with 5+ years of relevant industry experience, PhD/DVM with 3+ years, or bachelor’s degree with 10+ years of directly relevant experience.
  • 3–5 years of research experience involving neuroscience, tissue histology, or related preclinical research.
  • 3–5 years of hands-on preclinical in vivo research experience, including large-animal model testing.
  • 5+ years of medical device R&D experience involving biological safety risk assessments, or equivalent experience based on education.
  • Strong knowledge of ISO 10993, biocompatibility testing, biological evaluation, and regulated product development.
  • Experience developing study protocols, technical reports, testing strategies, and regulatory-supporting documentation.
  • Successful project management and cross-functional program experience.
  • Strong scientific presentation, written communication, problem-solving, and stakeholder-management skills.


This is an excellent opportunity for an experienced scientist to influence the research and development of innovative neuro-based medical technologies while serving as a trusted scientific advisor across the organization.

Apply