We are committed to collaborating with sponsors to drive innovation and accelerate the development ... Role Description The Preclinical Study Director for Ophthalmology will oversee and manage ...
We are committed to collaborating with sponsors to drive innovation and accelerate the development ... Role Description The Preclinical Study Director for Ophthalmology will oversee and manage ...
Director of Preclinical Research
Durham, NC · On-site +1
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 ...
Director of Preclinical Research
Durham, NC · On-site +1
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 ...
Vice President, Clinical Development
Raleigh, NC · On-site
$180 - $260/hr
... preclinical development, pharmacokinetics, clinical monitor / medical director (MD). Requirements * Strong scientific and clinical development background spanning small molecules and biologic ...
New
Vice President, Clinical Development
Raleigh, NC · On-site
$180 - $260/hr
... preclinical development, pharmacokinetics, clinical monitor / medical director (MD). Requirements * Strong scientific and clinical development background spanning small molecules and biologic ...
New
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 ...
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 ...
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 ...
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 ...
Director or Senior Director, Business Development
Raleigh, NC · On-site
$138K - $198K/yr
... preclinical and clinical research, regulatory affairs, and market access and reimbursement consulting. About This Role: We are seeking a motivated and experienced Director or Senior Director of ...
Director or Senior Director, Business Development
Raleigh, NC · On-site
$138K - $198K/yr
... preclinical and clinical research, regulatory affairs, and market access and reimbursement consulting. About This Role: We are seeking a motivated and experienced Director or Senior Director of ...
Preclinical development is also underway in coronary artery bypass grafts, pediatric heart surgery ... The Executive Director, Clinical Development & Medical Affairs is responsible for leadership and ...
Quick apply
Preclinical development is also underway in coronary artery bypass grafts, pediatric heart surgery ... The Executive Director, Clinical Development & Medical Affairs is responsible for leadership and ...
This position will function within the Quality Assurance Unit of Corporate Preclinical Development ... direct support of 21 CFR Part 58, ISO 17025, and the overall Quality System. * Quality Assurance ...
This position will function within the Quality Assurance Unit of Corporate Preclinical Development ... direct support of 21 CFR Part 58, ISO 17025, and the overall Quality System. * Quality Assurance ...
Principal Medical Writier
Durham, NC · On-site
... the Director of Medical Writing (or above). Key Responsibilities * Lead the development of high ... preclinical development will also be considered * Strong knowledge of global regulatory ...
New
Principal Medical Writier
Durham, NC · On-site
... the Director of Medical Writing (or above). Key Responsibilities * Lead the development of high ... preclinical development will also be considered * Strong knowledge of global regulatory ...
New
... the Director of Medical Writing (or above). Key Responsibilities * Lead the development of high ... preclinical development will also be considered * Strong knowledge of global regulatory ...
New
... the Director of Medical Writing (or above). Key Responsibilities * Lead the development of high ... preclinical development will also be considered * Strong knowledge of global regulatory ...
New
... preclinical through clinical development and commercialization. * Provide regulatory guidance on ... Direct experience with AAV, lentiviral, or other gene therapy platforms. * Experience with rare ...
Quick apply
... preclinical through clinical development and commercialization. * Provide regulatory guidance on ... Direct experience with AAV, lentiviral, or other gene therapy platforms. * Experience with rare ...
... preclinical through clinical development and commercialization. * Provide regulatory guidance on ... Direct experience with AAV, lentiviral, or other gene therapy platforms. * Experience with rare ...
Quick apply
... preclinical through clinical development and commercialization. * Provide regulatory guidance on ... Direct experience with AAV, lentiviral, or other gene therapy platforms. * Experience with rare ...
Associate Director, Quantitative Systems Pharmacology
Durham, NC · On-site
$152 - $253/hr
As an Associate Director of Quantitative Systems Pharmacology (QSP) Expert, you will develop and ... in drug research and development; contribute to preclinical and clinical study design and ...
New
Associate Director, Quantitative Systems Pharmacology
Durham, NC · On-site
$152 - $253/hr
As an Associate Director of Quantitative Systems Pharmacology (QSP) Expert, you will develop and ... in drug research and development; contribute to preclinical and clinical study design and ...
New
As an Associate Director of Quantitative Systems Pharmacology (QSP) Expert, you will develop and ... in drug research and development; contribute to preclinical and clinical study design and ...
As an Associate Director of Quantitative Systems Pharmacology (QSP) Expert, you will develop and ... in drug research and development; contribute to preclinical and clinical study design and ...
Speak with your direct manager to discuss your interest and alignment with your development goals ... on preclinical and clinical samples to support our gene therapy programs. This position requires ...
Speak with your direct manager to discuss your interest and alignment with your development goals ... on preclinical and clinical samples to support our gene therapy programs. This position requires ...
Speak with your direct manager to discuss your interest and alignment with your development goals ... on preclinical and clinical samples to support our gene therapy programs. This position requires ...
Speak with your direct manager to discuss your interest and alignment with your development goals ... on preclinical and clinical samples to support our gene therapy programs. This position requires ...
... preclinical, integrated medical school curriculum, Physician Assistant (PA) or Doctor of Physical ... Duties include participation in curriculum development and implementation, serving as an academic ...
... preclinical, integrated medical school curriculum, Physician Assistant (PA) or Doctor of Physical ... Duties include participation in curriculum development and implementation, serving as an academic ...
... on preclinical and clinical samples to support our gene therapy programs. This position requires ... Antibody assay development, qualification and validation activities will be performed in compliance ...
... on preclinical and clinical samples to support our gene therapy programs. This position requires ... Antibody assay development, qualification and validation activities will be performed in compliance ...
... on preclinical and clinical samples to support our gene therapy programs. This position requires ... Antibody assay development, qualification and validation activities will be performed in compliance ...
... on preclinical and clinical samples to support our gene therapy programs. This position requires ... Antibody assay development, qualification and validation activities will be performed in compliance ...
District Business Leader - Carolina East
Raleigh, NC · Remote
$170K - $200K/yr
... clinical and preclinical candidates in development for various psychiatric and neurological ... Plan, direct, implement, and oversee policies and activities for Territory Business Managers for a ...
District Business Leader - Carolina East
Raleigh, NC · Remote
$170K - $200K/yr
... clinical and preclinical candidates in development for various psychiatric and neurological ... Plan, direct, implement, and oversee policies and activities for Territory Business Managers for a ...
Director Preclinical Development information
See Raleigh, NC salary details
$39.4K - $49.5K
5% of jobs
$49.5K - $59.6K
9% of jobs
$67.2K is the 25th percentile. Wages below this are outliers.
$59.6K - $69.7K
15% of jobs
$69.7K - $79.8K
16% of jobs
The median wage is $83.2K / yr.
$79.8K - $90K
16% of jobs
$90K - $100.1K
14% of jobs
$100.6K is the 75th percentile. Wages above this are outliers.
$100.1K - $110.2K
10% of jobs
$110.2K - $120.3K
6% of jobs
$120.3K - $130.4K
4% of jobs
$130.4K - $140.6K
3% of jobs
$140.6K - $150.7K
2% of jobs
$39.4K
$89.8K
$150.7K
How much do director preclinical development jobs pay per year?
As of Aug 8, 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?
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 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 are popular job titles related to Director Preclinical Development jobs in Raleigh, NC? For Director Preclinical Development jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Director Preclinical Development jobs in Raleigh, NC look for? The top searched job categories for Director Preclinical Development jobs in Raleigh, NC are:
- Preclinical Development
- Fractional Sales Leadership
- Senior Director Implementation
- Associate Director Biopharma Pharmaceutical
- Director Corporate Philanthropy
- Director Leadership Development
- Director Telecommunications
- Director Of Assessment And Accreditation
- Director Global Learning Development
- Director Of Commercial Development
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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