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Preclinical Development Scientist Jobs (NOW HIRING)

Biocytogen

$67K - $92K/yr

Lead Evaluation and Development * Evaluate lead antibodies for binding, function, and developability, ensuring readiness for preclinical development. Collaboration and Reporting * Work with discovery ...

Prellis Biologics, Inc.

Position Summary We are seeking a Principal Scientist -- Bioanalysis to join our Protein Sciences ... preclinical development of Prellis's next‑generation biologic candidates, including ...

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How much do preclinical development scientist jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for preclinical development scientist in the United States is $38.66, according to ZipRecruiter salary data. Most workers in this role earn between $28.37 and $46.15 per hour, depending on experience, location, and employer.

What does a preclinical development scientist do?

A Preclinical Development Scientist is responsible for designing and conducting laboratory studies to evaluate the safety, efficacy, and pharmacological properties of new drug candidates before they are tested in humans. Their work involves planning experiments, analyzing data, and ensuring studies comply with regulatory standards. They collaborate with multidisciplinary teams, prepare technical reports, and contribute to the decision-making process about whether a drug can advance to clinical trials. Their efforts are crucial in identifying potential risks and optimizing drug formulations for further testing.

What skills and qualifications are needed to be a preclinical development scientist?

To thrive as a Preclinical Development Scientist, you need a strong background in biological sciences, pharmacology, or toxicology, typically supported by an advanced degree (MS or PhD) and relevant laboratory experience. Familiarity with GLP (Good Laboratory Practice) regulations, data analysis software, and preclinical testing platforms is essential. Strong analytical thinking, attention to detail, and effective communication skills help you interpret results and collaborate across multidisciplinary teams. These skills ensure the generation of reliable data to guide drug development decisions and support regulatory submissions.

What are common challenges faced by preclinical development scientists during the drug development process?

Preclinical Development Scientists often encounter challenges such as optimizing experimental models to accurately predict human responses, ensuring compliance with regulatory guidelines, and managing tight project timelines. Collaborating with interdisciplinary teams—including chemists, biologists, and toxicologists—is crucial for troubleshooting unexpected results or technical setbacks. Adapting to evolving scientific technologies and balancing multiple projects simultaneously are also key aspects of the role, making strong organizational and communication skills essential.

What are popular job titles related to Preclinical Development Scientist jobs?

For Preclinical Development Scientist jobs, the most frequently searched job titles are:

Infographic showing various Preclinical Development Scientist job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, and 2% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $80,420 per year, or $38.7 per hour.

Research And Development Scientist

Jacksonville, FL • On-site

Amaris Consulting
See more jobs at Amaris Consultingexternal

Other

This job post has expired 1 day ago. Applications are no longer accepted.

Key responsibilities

  • Support research activities and technical investigations for neuro medical device development, including new and sustaining products with stereotactic integration

  • Coordinate, initiate, and track preclinical/laboratory studies, biological safety assessments, and testing programs, including biocompatibility testing per ISO 10993

  • Develop, review, and approve scientific documentation, including study protocols, reports, and biological safety risk assessments

Job description

We are seeking a Research & Development Scientist to support the identification, assessment, and development of new and existing neuro-oncology, neuro-endoscopy, neurosurgery, and stereotactic-integrated neuro technologies. This role serves as a scientific and technical resource across biological safety evaluation, preclinical research, and cross-functional product development activities for a portfolio of neuro-specific medical devices. Priority will be given to candidates with a strong background in neuroscience, biological safety, and medical device R&D, ideally from neurotechnology, neurosurgery, neuro-oncology, neuro-endoscopy, or other advanced medical device environments.


Location: Jacksonville (Florida, US)

Work Mode: Hybrid

Contract Type: C2C

Schedule: Monday–Friday, 8:00 AM–5:00 PM, with flexibility available



Key Responsibilities

  • Lead or support research activities and technical investigations for neuro medical device development, including new and sustaining products with stereotactic integration
  • Coordinate, initiate, and track preclinical/laboratory studies, biological safety assessments, and testing programs, including biocompatibility testing per ISO 10993
  • Develop, review, and approve scientific documentation, including study protocols, reports, and biological safety risk assessments
  • Contribute biological safety content and scientific/technical expertise supporting regulatory submissions
  • Serve as the subject matter resource for biological evaluation activities across cross-functional teams (research, marketing, global sales, medical information) and external partners
  • Present research findings, technical reviews, and data to internal stakeholders, KOLs, laboratories, and regulatory bodies
  • Support and maintain scientific relationships with key opinion leaders and external collaborators
  • Contribute to additional neuro-related research activities based on business and project needs



Required Qualifications

  • Master's degree in a relevant scientific discipline (neuroscience, biomedical science, biology, toxicology, materials science, or related field) required; PhD or DVM preferred. Bachelor's degree with significant directly relevant experience may be considered in lieu of an advanced degree
  • Typically requires: Master's + 5 years relevant industry experience, or PhD/DVM + 3 years relevant industry experience, or Bachelor's + 10 years relevant experience
  • 3–5 years of research experience in neuroscience, tissue histology, or related preclinical research areas
  • 3–5 years of hands-on preclinical in vivo research experience, including large animal model testing
  • 5+ years of experience in medical device R&D with responsibility for biological safety risk assessment, or equivalent depth of experience based on degree level
  • Strong experience with biological safety assessments and regulated product development
  • Proven project management experience

Preferred Qualifications

  • Experience supporting regulated product development and cross-functional research programs
  • Background in neurotechnology, neurosurgery, neuro-oncology, or neuro-endoscopy environments



Why choose us

  • An international community bringing together more than 110 different nationalities
  • An environment where trust is central: 70% of our leaders started their careers at the entry level
  • A strong training system with our internal Academy and more than 250 modules available
  • A dynamic work environment that frequently comes together for internal events (afterworks, team buildings, etc.)


Amaris Consulting promotes equal opportunities. We are committed to bringing together people from diverse backgrounds and creating an inclusive work environment. In this regard, we welcome applications from all qualified individuals, regardless of sex, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.

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