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Study Director Jobs in Raleigh, NC (NOW HIRING)

IQVIA

Associate Director, Study Operations

Durham, NC · Remote

$102K - $285K/yr

Associate Director, Study Operations, Rater Services Location: Home-based in USA/Canada Job Overview Associate Clinical Project Management Directors supervise, manage and provide oversight to ...

New

IQVIA

Associate Director, Study Operations

Durham, NC · Remote

$102K - $285K/yr

Associate Director, Study Operations, Rater Services Location: Home-based in USA/Canada Job Overview Associate Clinical Project Management Directors supervise, manage and provide oversight to ...

New

Doist

Clinical Study Design Manager

Morrisville, NC · On-site

$110 - $160/hr

The Clinical Study Design Manager is responsible for working with our clients and internal staff to ... Lead the build, testing, and implementation of direct data capture services, ensuring system ...

Science 37

Clinical Study Design Manager

Raleigh, NC · On-site

$120 - $170/hr

The Clinical Study Design Manager is responsible for working with our clients and internal staff to ... Lead the build, testing, and implementation of direct data capture services, ensuring system ...

CTI

Study Activation Manager

Raleigh, NC · On-site

Ability to influence and align cross-functional stakeholders without direct authority. * Ability to ... in study start-up, site activation, clinical operations, or clinical trial management. About CTI ...

CTI

Study Activation Manager

Raleigh, NC · On-site

Ability to influence and align cross-functional stakeholders without direct authority. * Ability to ... in study start-up, site activation, clinical operations, or clinical trial management. About CTI ...

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Study Director information

See Raleigh, NC salary details

$43.7K

$124.8K

$226K

How much do study director jobs pay per year?

As of Aug 27, 2026, the average yearly pay for study director in Raleigh, NC is $124,783.00, according to ZipRecruiter salary data. Most workers in this role earn between $56,400.00 and $183,200.00 per year, depending on experience, location, and employer.

What is a study director?

A Study Director is the individual responsible for the overall conduct of a scientific study, particularly in regulated environments such as pharmaceuticals, chemicals, or environmental research. They oversee the planning, execution, and reporting of studies to ensure they comply with regulatory standards, such as Good Laboratory Practice (GLP). The Study Director acts as the main point of control and communication, coordinating among team members and ensuring that the study meets its scientific and regulatory objectives. Their role is critical for the integrity and quality of the data generated.

What does a study director do?

As a study director, your job is to manage studies, analyze results, and interpret reports so you can deliver a summary of the findings. This work has three categories. First, on the technical side, your job includes creating the plan for the study, coordinating with other scientists, and overseeing data collection. In the administrative role, you monitor junior employees and ensure each investigation finishes within budgetary constraints. In the compliance role, you ensure that each study happens under strict safety and ethics protocols. You may be asked to run multiple studies at the same time, adding to the complexity of this position.

How does a study director typically collaborate with cross-functional teams during a research project?

As a Study Director, you play a central role in coordinating research activities by regularly collaborating with scientists, technicians, quality assurance personnel, and regulatory teams. You are responsible for ensuring all team members are aligned on study objectives, timelines, and compliance requirements. Effective communication and leadership are essential, as you facilitate meetings, delegate tasks, and resolve issues that arise to keep the project on track. This collaborative environment not only fosters professional growth but also provides valuable exposure to various scientific and operational domains within the organization.

What skills and qualifications does a successful study director have?

To thrive as a Study Director, you need a solid background in scientific research methods, regulatory compliance, and study protocol development, usually supported by an advanced degree in life sciences or a related field. Familiarity with laboratory information management systems (LIMS), Good Laboratory Practice (GLP) standards, and project management tools is highly valued. Strong leadership, attention to detail, and effective communication are crucial soft skills for managing cross-functional teams and ensuring study integrity. These competencies are vital to ensure regulatory adherence, data accuracy, and successful project outcomes in research environments.

What is the difference between Study Director vs Laboratory Manager?

AspectStudy DirectorLaboratory Manager
CredentialsTypically requires advanced degrees (e.g., MS, PhD) and relevant certificationsRequires relevant degrees and management experience, but not necessarily advanced research credentials
Work EnvironmentLeads specific research or regulatory studies, often in contract labs or pharmaceutical companiesOversees daily lab operations, staff, and compliance across multiple projects
Industry UsageCommonly used in GLP, clinical, and research settingsUsed broadly in laboratory settings across industries

The Study Director focuses on designing, overseeing, and ensuring the integrity of specific studies, often requiring scientific expertise. The Laboratory Manager handles overall lab operations, staff management, and compliance. Both roles are essential but differ in scope and responsibilities.

More about Study Director jobs

What are the most commonly searched types of Study jobs in Raleigh, NC?

The most popular types of Study jobs in Raleigh, NC are:

What are popular job titles related to Study Director jobs in Raleigh, NC?

For Study Director jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Study Director jobs in Raleigh, NC look for?

The top searched job categories for Study Director jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Study Director jobs?

Cities near Raleigh, NC with the most Study Director job openings:

Study Director jobs near you
Infographic showing various Study Director job openings in Raleigh, NC as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $124,783 per year, or $60 per hour.

Clinical Project Management Director, Cell & Gene Therapy - Global Study Leadership

IQVIA, Inc.

Durham, NC • On-site

Full-time

Posted 28 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 225 rated it services

Job description

We are seeking an accomplished Clinical Project Management Director to join our Customer-Dedicated Delivery Unit, leading complex global oncology programs and partnering with senior sponsor stakeholders to shape the future of cancer research. This is a highly strategic leadership role offering the opportunity to influence development strategy, drive operational excellence, and oversee the successful execution of innovative clinical studies that have the potential to transform patient outcomes.
The ideal candidate will bring deep oncology expertise, including significant experience leading complex global oncology studies and programs. Experience in Cell & Gene Therapy (CGT), including CAR-T, gene editing, or other advanced therapies, is strongly preferred.
As a trusted partner to our customers, you will lead high-profile programs, guide cross-functional teams, and shape operational strategy across some of the industry's most innovative clinical development initiatives. This role offers the opportunity to work at the forefront of oncology innovation, supporting studies across established and emerging therapeutic modalities, including Cell & Gene Therapy.
What You'll Do
  • Strategic Project & Program Leadership: Lead the delivery of large, complex global clinical studies and multi-study programs, translating customer objectives into effective operational strategies and execution plans
  • Portfolio Oversight: Provide operational leadership across programs and portfolios, ensuring consistency, quality, financial performance, and successful delivery of clinical milestones
  • Customer Partnership: Serve as the primary senior contact for sponsors, building trusted relationships, managing escalations, and driving collaborative solutions to achieve shared goals
  • Cross-Functional Leadership: Lead and align global, matrixed teams across clinical operations, data management, safety, regulatory, and other functional areas to ensure seamless execution
  • Risk Management & Problem Solving: Proactively identify operational and strategic risks, implement mitigation plans, and lead issue resolution efforts to maintain project momentum and performance
  • Financial Accountability: Oversee program financial performance, resource planning, forecasting, scope management, and change control activities to support successful business outcomes
  • Business Development Support: Contribute to proposal development, strategic planning, and bid defense activities for large, multi-service clinical opportunities
  • Continuous Improvement: Drive innovation, process optimization, and the implementation of best practices to enhance delivery efficiency, quality, and customer satisfaction
  • Team Development: Mentor and develop project leaders and cross-functional team members, fostering a culture of accountability, collaboration, and professional growth

What We're Looking For
  • 12-15+ years of experience in clinical research, clinical operations, and/or project leadership within the pharmaceutical, biotechnology, or CRO industry, including substantial experience leading large, global Phase I-IV oncology studies and development programs
  • Deep oncology therapeutic expertise is required, with a strong preference for experience leading Cell & Gene Therapy (CGT), CAR-T, TCR-T, gene editing or other Advanced Therapy Medicinal Product (ATMP) programs
  • Demonstrated success leading complex global oncology portfolios and building trusted relationships with executive-level stakeholders
  • Proven success leading large, global, multi-regional clinical studies, programs, or portfolios with operational and financial responsibility
  • Strong understanding of clinical trial conduct, ICH-GCP guidelines and applicable regulatory requirements
  • Demonstrated ability to build and maintain executive-level customer relationships and successfully manage complex stakeholder environments
  • Experience leading matrixed, cross-functional teams in a global environment
  • Strong strategic thinking, problem-solving and risk management capabilities
  • Excellent communication, presentation and influencing skills
  • Bachelor's degree in Life Sciences or a related field required; advanced degree preferred

Leadership Profile
  • Influential oncology leader with deep therapeutic expertise and the ability to shape strategy, build trust, and drive alignment across customers, executives and global teams
  • Strategic thinker who transforms complex challenges into clear, actionable solutions
  • Confident decision-maker who thrives in fast-paced, highly matrixed environments
  • Commercially savvy with a strong customer focus and a track record of building enduring partnerships
  • Proven leader of large-scale global clinical programs, delivering operational, financial and quality excellence
  • Passionate people leader who develops talent, inspires high performance and builds accountable, high-performing teams

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role, when annualized, is $125,900.00 - $350,900.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

What IQVIA employees say

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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