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Contract Research Jobs in Raleigh, NC (NOW HIRING)

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Director of Preclinical Research

Durham, NC · On-site +1

Identify appropriate opportunities to outsource projects to contract research vendors to advance our goals * Oversee all aspects of the vendor management process including selection, project scoping ...

INC Research

Biometrics Project Manager

Raleigh, NC

Project management experience in a contract research organization, pharmaceutical, or biotechnology company. Experience actively managing clinical research projects across biometrics functional areas.

INC Research

Biometrics Project Manager

Raleigh, NC · On-site

Project management experience in a contract research organization, pharmaceutical, or biotechnology company. Experience actively managing clinical research projects across biometrics functional areas.

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How much do contract research jobs pay per hour?

As of Jul 19, 2026, the average hourly pay for contract research in Raleigh, NC is $43.38, according to ZipRecruiter salary data. Most workers in this role earn between $22.07 and $47.40 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Contract Research Associate, and why are they important?

To thrive as a Contract Research Associate, you need a background in life sciences or a related field, strong research methodology knowledge, and often a relevant degree (such as a BSc or MSc). Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) certification, and data analysis tools like SPSS or SAS are typically required. Attention to detail, strong organizational skills, and effective communication are vital soft skills for coordinating studies and managing stakeholders. These abilities ensure high-quality, compliant research execution and reliable study outcomes within regulatory frameworks.

What is contract research?

Contract research refers to research services provided by an external organization, known as a Contract Research Organization (CRO), to other businesses, academic institutions, or government agencies. These services often include conducting clinical trials, laboratory testing, data analysis, or product development on a contractual basis. Contract research allows companies to access specialized expertise, reduce costs, and focus on their core activities while outsourcing complex or resource-intensive research tasks.

What are some common challenges faced by professionals in contract research roles and how can they be managed?

Professionals in contract research often navigate tight deadlines, shifting client requirements, and the need to maintain strict regulatory compliance. Balancing multiple projects simultaneously and communicating effectively with both internal teams and external sponsors can be demanding. Proactively managing workload, staying organized, and maintaining clear, consistent communication with stakeholders are key strategies to overcome these challenges. Additionally, staying updated on industry regulations and leveraging project management tools can help ensure successful outcomes.
What are the most commonly searched types of Research jobs in Raleigh, NC? The most popular types of Research jobs in Raleigh, NC are:
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What job categories do people searching Contract Research jobs in Raleigh, NC look for? The top searched job categories for Contract Research jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Contract Research jobs? Cities near Raleigh, NC with the most Contract Research job openings:
Contract Research jobs near you
Infographic showing various Contract Research job openings in Raleigh, NC as of July 2026, with employment types broken down into 1% As Needed, 62% Full Time, 21% Part Time, 1% Temporary, and 15% Contract. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $90,227 per year, or $43.4 per hour.

Preclinical Study Project Manager

Powered Research, LLC

Durham, NC • On-site

$64K - $82K/yr

Other

Re-posted 9 days ago

Job description

Company Description Powered Research, LLC is a leading preclinical contract research organization (CRO) specializing in non-GLP ophthalmology and oncology models for life science R&D companies. Based at a single site in Durham, NC, the company’s team of approximately 70 scientists, veterinarians, and technical experts has led thousands of preclinical studies with high scientific rigor. Powered Research focuses on transforming early discoveries into validated product candidates through collaborative, world-class preclinical research. Guided by integrity, excellence, and a commitment to improving human health, the organization aims to be the premier global partner for comprehensive preclinical research. Sponsors can easily access Powered Research’s ophthalmology and oncology services through its Science Exchange storefront for streamlined collaboration and project management.

Role Description The Preclinical Study Project Manager is a full-time, on-site role based in Durham, NC. This position is responsible for planning, coordinating, and overseeing preclinical ophthalmology and oncology studies from initiation through completion, ensuring timelines, quality standards, and Sponsor expectations are met. Day-to-day activities include developing study plans and schedules, tracking milestones, managing resources, monitoring study progress, and proactively resolving operational issues. The role involves close collaboration with scientists, veterinarians, technicians, and external Sponsors to clarify requirements, align expectations, and maintain clear communication throughout the study lifecycle. The Preclinical Study Project Manager will also support logistics related to materials, equipment, and samples, coordinate inspections and internal reviews as needed, and contribute to process improvements that enhance study efficiency and data quality.

Qualifications

  • Demonstrated project management skills, including experience planning, tracking, and delivering complex scientific or technical projects (e.g., Project Management, Expeditor, Expediting).
  • Experience coordinating logistics in a non-clinical research or laboratory setting, including scheduling, materials handling, and vendor or Sponsor coordination (e.g., Logistics Management, Expediting).
  • Familiarity with inspection, quality checks, or compliance processes in a scientific, preclinical, or laboratory environment (e.g., Inspection).
  • Strong organizational, time-management, and prioritization abilities with attention to detail and accuracy in documentation.
  • Excellent written and verbal communication skills, with the ability to interface effectively with cross-functional teams and external Sponsors.
  • Bachelor’s degree in a life science, veterinary science, or related field; advanced degree or equivalent relevant experience in preclinical research is a plus.
  • Previous experience in a CRO, pharmaceutical, biotechnology, or preclinical research environment, particularly in ophthalmology or oncology, is highly beneficial.
  • Proficiency with project management and collaboration tools, and comfort working in a fast-paced, deadline-driven setting.

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