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Contract Research Jobs in Raleigh, NC (NOW HIRING)

CEDENT

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 ...

Duke University

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

Serve as a primary liaison with sponsors, Contract Research Organizations (CROs), Investigational Drug Services (IDS), and internal stakeholders. * Lead study monitoring, audit preparation, and ...

Duke University

Clinical Research Coordinator

Durham, NC

$23.50 - $31.25/hr

Serve as a primary liaison with sponsors, Contract Research Organizations (CROs), Investigational Drug Services (IDS), and internal stakeholders. * Lead study monitoring, audit preparation, and ...

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.

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.

Jobtailor

Senior Director, Clinical Development

Cary, NC · On-site

$120 - $190/hr

Manage Key Opinion Leader and Medical Advisory Board interactions * Assist Clinical Operations with supervision of activities of contract research organizations by reviewing key study plans and ...

Jobtailor

Director, Product Management

Morrisville, NC · On-site

$120 - $180/hr

Deep understanding of the Contract Research Organization industry * Experience with Agile and Scrum methodologies and the ability to implement and adapt these practices across teams Core Competencies ...

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How much do contract research jobs pay per hour?

As of Aug 24, 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 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 the key skills and qualifications needed to thrive as a contract research associate?

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 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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For Contract Research jobs in Raleigh, NC, the most frequently searched job titles are:

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Contract Research jobs near you
Infographic showing various Contract Research job openings in Raleigh, NC as of August 2026, with employment types broken down into 50% Part Time, and 50% Contract. Highlights an 100% In-person job distribution, with an average salary of $90,227 per year, or $43.4 per hour.

Director of Research & Development

Valid8 Financial, Inc.

Cary, NC • On-site

$170 - $230/hr

Other

Posted 14 days ago

Job description

VQ Biomedical, based in the Research Triangle Park area of North Carolina, is an early-stage medical device company developing an innovative central venous catheter that delivers oxygen directly to the bloodstream in critically ill ICU patients suffering from lung injury and respiratory failure. VQ is developing the first minimally invasive alternative to mechanical ventilation and ECMO (extracorporeal membrane oxygenation) capable of delivering supplemental oxygen independent of the injured lungs, allowing them to rest, heal, and recover.

Position Summary

The Director of R&D plays a vital role in the leadership of the company. This person will craft and execute R&D strategy, build and lead the R&D team, and drive complex device development from concept through benchtop and preclinical testing and into early clinical evaluation, while ensuring FDA and ISO compliance throughout. This is a hands-on, early-phase role that pairs bench-level engineering with technical leadership. This is a full-time, in-person position that reports to the CEO.

Duties and Responsibilities
  • Develop and execute the R&D strategy and technical roadmap in support of the company’s development and regulatory milestones
  • Build, mentor, and directly manage the R&D team as the company scales
  • Lead the hands-on design, prototyping, and iteration of the oxygenation catheter and its components
  • Develop and execute benchtop testing to characterize and verify device performance
  • Own technical requirements, design inputs and outputs, and verification and validation planning as the design matures
  • Lead risk management activities, including risk analyses and mitigation, in accordance with ISO 14971
  • Establish and maintain the Design History File and supporting quality documentation for new designs and revisions to existing designs
  • Plan, execute, and support preclinical (in vivo) studies in partnership with contract research organizations and clinical experts, and translate findings into design improvements
  • Work cross-functionally with contract manufacturers to build prototypes, develop processes, and establish pilot manufacturing for new products
  • Partner with QA/RA to ensure all R&D activities adhere to ISO 13485, FDA 21 CFR Part 820, and GMP standards
  • Develop schedule and budget estimates, and take responsibility for achieving technical milestones on schedule and on budget
  • Support technical reporting and deliverables for federal grants and contracts
  • Other duties as directed
Skills / Qualifications
  • Bachelor’s or Master’s degree in engineering (biomedical, mechanical, or related field)
  • Minimum of 10 years of relevant medical device product development experience, preferably in a fast-paced small business or startup environment
  • Proven experience in medical device design, specifically catheter design and construction
  • Experience developing and documenting designs within an established, FDA-compliant quality system, including design controls, ISO 13485, and ISO 14971
  • Experience developing benchtop test methods and characterizing device performance
  • Experience planning and supporting preclinical or animal studies
  • Experience starting new manufacturing lines for new products
  • Familiarity with government contract and grant reporting
  • Proficiency with CAD
  • Ability to work in a fast-paced environment and work additional hours as required
  • Ability to adapt to a changing environment and identify and solve problems efficiently
  • Prior experience in a startup environment is a plus
  • Must be able to meet hospital credentialing requirements in order to observe products within a hospital environment

VQ Biomedical is interested in every qualified candidate who is eligible to work in the United States. However, we are not able to sponsor visas.

VQ Biomedical is an equal opportunity employer. As such, we provide employment opportunities without regard to race, color, religion, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, military service, or other characteristics protected by law.

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