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Preclinical Development Jobs in Raleigh, NC (NOW HIRING)

Administrative Ass3

Durham, NC · On-site

$16.50 - $21.75/hr

This position will function within the Operations and Planning Unit of Corporate Preclinical Development and Toxicology (CPDT) and will support the conduct of nonclinical laboratory investigations of ...

To date, we've developed a suite of research-enabling resources, funded or collaborated with over ... Oversee our preclinical grants portfolio and manage the entire lifecycle of grantmaking activities ...

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Preclinical Development information

See Raleigh, NC salary details

$32.1K

$82.7K

$125.4K

How much do preclinical development jobs pay per year?

As of Jul 10, 2026, the average yearly pay for preclinical development in Raleigh, NC is $82,671.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,900.00 and $87,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Preclinical Development position, and why are they important?

To excel in Preclinical Development, you need a solid background in biology, pharmacology, or related life science fields, often supported by an advanced degree and experience with laboratory research. Familiarity with Good Laboratory Practice (GLP) regulations, data analysis software, and animal study management systems is expected. Strong attention to detail, effective problem-solving skills, and the ability to communicate complex findings clearly are valuable soft skills. These competencies are essential to ensure the successful and compliant progression of drug candidates toward clinical trials.

What is a Preclinical Development job?

A Preclinical Development job involves overseeing the research and testing of drug candidates before they enter clinical trials. Professionals in this role design and conduct studies to assess a drug’s safety, efficacy, and pharmacokinetics using laboratory and animal models. They collaborate with scientists, regulatory experts, and project managers to generate data required for regulatory approval. Their work helps identify potential risks and optimize drug formulations before human testing begins.

What are the typical responsibilities of someone working in Preclinical Development?

Professionals in Preclinical Development are responsible for designing, conducting, and analyzing laboratory and animal studies to evaluate the safety and efficacy of new drug candidates before clinical trials. They often collaborate closely with research scientists, regulatory teams, and project managers to ensure studies meet compliance standards and scientific objectives. Daily tasks may include developing protocols, interpreting data, preparing regulatory documentation, and troubleshooting experimental issues. This role offers opportunities to gain broad exposure to the drug discovery process and can lead to advancement into project leadership or regulatory affairs positions.

What are the most commonly searched types of Preclinical Development jobs in Raleigh, NC? The most popular types of Preclinical Development jobs in Raleigh, NC are:
What are popular job titles related to Preclinical Development jobs in Raleigh, NC? For Preclinical Development jobs in Raleigh, NC, the most frequently searched job titles are:
Infographic showing various Preclinical Development job openings in Raleigh, NC as of July 2026, with employment types broken down into 1% As Needed, 78% Full Time, 17% Part Time, 1% Temporary, and 3% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $82,671 per year, or $39.7 per hour.
Administrative Ass3

Administrative Ass3

MILLENNIUMSOFT

Durham, NC • On-site

$16.50 - $21.75/hr

Other

Re-posted 26 days ago


Job description

Position : Administrative Ass3

Location : Research Triangle Park, NC

Duration : 12 months contract

Total Hours/week : 40.00

1st shift

Description:

  • This position will function within the Operations and Planning Unit of Corporate Preclinical Development and Toxicology (CPDT) and will support the conduct of nonclinical laboratory investigations of medical devices and materials in accordance with GLP regulations and the Client CPDT Quality System.
  • This position provides operational support by facilitating department workflows, coordinating testing activities, and providing client support from project initiation to completion for R&D projects from initiation through completion.
  • This is a perfect opportunity for someone with some analytical chemistry experience that wants to transition their career towards project management.