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Director Preclinical Development Jobs in Raleigh, NC

To date, we've developed a suite of research-enabling resources, funded or collaborated with over ... hiring a Director of Preclinical Research to help us pursue a growing number of research ...

Senior Director, Drug Development Location: Home-based in USA/Europe Job Overview: Manages a ... preclinical strategy, clinical strategy, regulatory strategy, and commercial strategy. * Support ...

Senior Director, Drug Development Location: Home-based in USA/Europe Job Overview: Manages a ... preclinical strategy, clinical strategy, regulatory strategy, and commercial strategy. * Support ...

Supply strategic regulatory guidance for global drug development efforts, covering areas such as ... A scientific grounding in immunology, cell biology, and preclinical assays. * Experience preparing ...

Speak with your direct manager to discuss your interest and alignment with your development goals ... our preclinical therapeutic pipeline. The ideal candidate will have hands-on experience with ...

Speak with your direct manager to discuss your interest and alignment with your development goals ... our preclinical therapeutic pipeline. The ideal candidate will have hands-on experience with ...

Speak with your direct manager to discuss your interest and alignment with your development goals ... preclinical gene therapy pipeline. The Research Associate II will work closely with scientists ...

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Director Preclinical Development information

See Raleigh, NC salary details

$39.4K

$89.8K

$150.7K

How much do director preclinical development jobs pay per year?

As of Jul 19, 2026, the average yearly pay for director preclinical development in Raleigh, NC is $89,806.00, according to ZipRecruiter salary data. Most workers in this role earn between $68,000.00 and $105,500.00 per year, depending on experience, location, and employer.

What is a Director Preclinical Development job?

A Director of Preclinical Development oversees the early-stage research and testing of drug candidates before they enter clinical trials. They manage preclinical studies, ensuring regulatory compliance, safety, and efficacy assessments. This role involves coordinating with cross-functional teams, external partners, and regulatory agencies to advance promising compounds. Strong expertise in toxicology, pharmacology, and regulatory guidelines is essential. The director plays a key role in shaping the preclinical strategy to support successful drug development.

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

To thrive as a Director Preclinical Development, you need deep expertise in pharmaceutical or biotechnology research, strong project management abilities, and an advanced degree (Ph.D., Pharm.D., or equivalent) in a life sciences field. Familiarity with regulatory guidelines (such as GLP), experience using data management and statistical analysis software, and prior leadership roles in preclinical studies are essential. Exceptional communication, problem-solving, and team leadership skills set candidates apart in managing multidisciplinary teams and collaborative projects. These competencies are crucial for successfully guiding drug candidates through preclinical stages while ensuring regulatory compliance and timely project delivery.

What are the typical responsibilities and team dynamics for a Director of Preclinical Development?

A Director of Preclinical Development is responsible for overseeing the planning, execution, and management of preclinical research programs, ensuring that studies meet scientific, regulatory, and project milestones. You will typically work with cross-functional teams including toxicologists, pharmacologists, regulatory affairs professionals, and external partners, fostering collaboration throughout the drug development process. The role often involves reviewing study designs and data, preparing regulatory submissions, and providing strategic direction to advance compounds toward clinical testing. Working closely with upper management, you'll play a key part in shaping research priorities and resource allocation. This position offers significant influence over drug development strategies and opportunities for advancement to higher executive or scientific leadership roles.

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 cities near Raleigh, NC are hiring for Director Preclinical Development jobs? Cities near Raleigh, NC with the most Director Preclinical Development job openings:
Infographic showing various Director 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 $89,806 per year, or $43.2 per hour.

Preclinical Study Director Ophthalmology

Powered Research, LLC

Durham, NC โ€ข On-site

Other

Re-posted 27 days ago


Job description

Company Description

Powered Research is a leading preclinical contract research organization (CRO) specializing in non-GLP models for ophthalmology and oncology research. Based in Durham, NC, our team of 70 dedicated experts has conducted thousands of preclinical studies since 2012, adhering to the highest standards of scientific rigor. We are committed to collaborating with sponsors to drive innovation and accelerate the development of transformative therapies. Our mission is to provide tailored, cutting-edge solutions that advance scientific progress and impact human health worldwide.

Role Description

The Preclinical Study Director for Ophthalmology will oversee and manage preclinical studies from conception to completion. Responsibilities include developing study protocols, designing and executing research, ensuring compliance with regulatory guidelines, managing data analysis, and preparing comprehensive study reports. You will collaborate with cross-functional teams to ensure the accuracy, quality, and timeliness of project deliverables. This is a full-time, on-site role located in Durham, NC.


Qualifications

  • Proficiency in Laboratory Skills, with a focus on preclinical methodology and testing
  • Experience in Research, with a background in study design, data collection, and scientific analysis
  • In-depth knowledge of drug discovery and development in preclinical studies
  • Strong skills in disease model development
  • Expertise in In Vivo study techniques, including handling animal models in ophthalmology research
  • Strong attention to detail and commitment to scientific rigor
  • Exceptional communication and organizational skills
  • Advanced degree in biology, toxicology, pharmacology, or a related field; PhD or DVM preferred