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Study Director Jobs in Raleigh, NC (NOW HIRING)

NCSU

Study Director - IR-4 Project

Raleigh, NC

Posting Information Posting Number PG194770EP Internal Recruitment No Working Title Study Director - IR-4 Project Anticipated Hiring Range Commensurate with Experience ($80,000 - $95,000) Work ...

MedPharm

Study Director/Senior Scientist

Durham, NC · On-site

The title, Study Director, refers to the individual responsible for the scientific conduct of assigned studies and should not be interpreted as department head, manager, director, etc. While this is ...

MedPharm

Study Director/Senior Scientist

Durham, NC · On-site

The title, Study Director , refers to the individual responsible for the scientific conduct of assigned studies and should not be interpreted as department head, manager, director, etc. While this is ...

IQVIA

Senior Global Clinical Study Manager

Durham, NC · On-site

Required Experience * 2+ years of global study management experience * Experience across multiple ... Make a direct impact on patient outcomes worldwide IQVIA is a leading global provider of clinical ...

AskBio

Director, Pathology

Durham, NC

The Director, Pathology will provide comprehensive support for nonclinical studies, including primary histopathology and pathology peer reviews, interpretation of all nonclinical study data/findings ...

AskBio

Director, Pathology

Durham, NC · On-site

The Director, Pathology will provide comprehensive support for nonclinical studies, including primary histopathology and pathology peer reviews, interpretation of all nonclinical study data/findings ...

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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 6, 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 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.

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.

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 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.

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.
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.

Study Director - IR-4 Project

NCSU

Raleigh, NC

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 14 days ago

North Carolina State University rating

6.8

Company rating: 6.8 out of 10

Based on 33 frontline employees who took The Breakroom Quiz

456th of 615 rated colleges and universities

Job description

Posting Information
Posting Number PG194770EP Internal Recruitment No Working Title Study Director - IR-4 Project Anticipated Hiring Range Commensurate with Experience ($80,000 - $95,000) Work Schedule Monday - Friday / 40 hours/week (regular in-person attendance is required) Job Location Raleigh, NC Department IR-4 Project About the Department
The IR-4 Project is a nationally and internationally recognized Federal-State partnership that facilitates the registration of safe and effective chemical, biological, and other pest management technologies for specialty crop producers. Specialty crops-including fruits, vegetables, nuts, herbs, spices, ornamentals, and nursery crops-represent high-value sectors of U.S. agriculture but often lack sufficient market incentives for private industry to independently pursue registrations for these crops.
As the nation's primary program supporting pest management solutions for specialty crops, IR-4 plays a critical role in ensuring growers have access to the tools needed to produce safe, abundant, and economically viable crops. Without IR-4, many specialty crop growers would have limited access to crop protection products, resulting in reduced productivity, increased pest losses, and fewer management options.
IR-4 operates through a nationwide network consisting of four regional programs, multiple USDA and university partners, more than 20 public research farms, and analytical laboratories located throughout the United States. The program coordinates research conducted by approximately 125 scientists and technical specialists across the country.
IR-4 Project Headquarters is part of North Carolina State University and located in Centennial Campus in Raleigh, North Carolina, within the Venture IV Building. Headquarters provides national leadership, scientific oversight, regulatory strategy, data management, and Good Laboratory Practice (GLP) compliance for the program's research portfolio and regulatory submissions.
Wolfpack Perks and Benefits
As a Pack member, you belong here, and can enjoy exclusive perks designed to enhance your personal and professional well-being. As you consider this opportunity, we encourage you to review our Employee Value Proposition and learn more about what makes NC State the best place to learn and work for everyone.

What we offer:
  • Medical, Dental, and Vision
  • Flexible Spending Account
  • Retirement Programs
  • Disability Plans
  • Life Insurance
  • Accident Plan
  • Paid Time Off and Other Leave Programs
  • 12 Holidays Each Year
  • Tuition and Academic Assistance
  • And so much more!

Attain Work-life balance with our Childcare benefits, Wellness & Recreation Membership, and Wellness Programs that aim to build a thriving wolfpack community.
Disclaimer: Perks and Benefit eligibility is based on Part-Time or Full-Time Employment status. Eligibility and Employer Sponsored Plans can be found within each of the links offered.
Essential Job Duties
The Study Director position will report directly to the IR-4 Submission Manager and Senior Study Director. This position will be an integral part of the IR-4 Project Headquarters unit. Duties of this position include, but are not limited to:
Protocol Development (30%): Provide technical direction of research associated with IR-4 Project Magnitude of the Residue Studies that are performed by cooperating university and government scientists at various locations throughout North America. All aspects of the study must follow the provisions of the United States Environmental Protection Agency's Federal Good Laboratory Practice (Chapter 40- Code of Federal Regulations, Part 160) regulations. Specific duties include development of approximately 10 national research protocols (study plans) annually for IR-4 Project sanctioned studies. Responsible for drafting and developing protocols after extensive consultation with owners of the products, study scientists and IR-4 Project biologists. Must be able to balance needs of stakeholder suggestions in the development of the final product. Protocols must be prepared and authorized well in advance of target dates for research.

Study Coordination (30%): Direct and manage approximately 60 on-going IR-4 sponsored residue research studies in various phases of completion. An average IR-4 residue study involves seven field trials and one analytical phase performed at various research facilities. This means that the Study Director is responsible to direct the research of 400 research projects. As autonomous director of the projects, the study director must assist scientists to successfully plan, conduct and report on IR-4 sponsored research with chemical and bio-based pesticides on specialty crops. Must promptly evaluate and approve all proposed modifications from the authorized research protocol. Must keep track of status of active studies, including knowledge when critical phases of research are planned/performed, when residue samples are shipped to the analytical laboratory, when samples are analyzed by the laboratory and when research reports are received. Communicate with numerous individuals to maintain involvement in all facets of the research. Also responsible for critical review and scientific assessment of the data/data reports associated with the studies in a timely manner to ensure that the research was performed appropriately and according to protocol. Review includes the test substance application rates, application timing of the test substance collection of adequate residue samples, and appropriate storage of samples before and during shipping to the laboratory, review of the analytical data including the analytical summary report. All findings of the Quality Assurance unit must be promptly addressed.
Data package development (30%): Independently develop approx. 6 "submission ready" data packages annually utilizing established national (USEPA-OPPTS GUIDELINES) and/or international standards (e.g. UN FAO-Joint Meeting on Pesticide Residues). Expectations are that the incumbent:
  • Prepare quality reports that are easily reviewed by all parties (Quality Assurance Unit, IR-4 Management, Cooperating Company, US EPA, others). When something is missing, identify the gap, solicit information and/or data for performing facilities in order to close data gaps, then compose summaries and existing data/info in correct format. This must be completed under IR-4 established timelines.
  • Maximize value of existing research through the use of extrapolation models and crop groups, reduced data requirement proposals, and/or broad use pattern. Communicate with personnel in all facets of the project in a professional manner to complete projects in accordance with timelines.
  • Assist other Study Directors in preparing reports and interpreting data.
Other Responsibilities
Other responsibilities as assigned (10%)
  • Attend IR-4, grower, and professional meetings, make presentations and join committees of appropriate groups.
  • Travel is an expectation of this position (3-6 times per year).
  • Assist other Study Directors and the Senior Study Directors in completion of projects.
  • Work in a cooperative manner with other individuals at Headquarters and elsewhere.
  • General duties at IR-4 Headquarters include maintaining support for the office and research programs.
Qualifications
Minimum Education and Experience
  • Requires possession of post-baccalaureate credentials or a comparable record of independent research productivity.
Other Required Qualifications
  • Ability to maintain attention to details, prioritize and meet deadlines.
  • Excellent oral, written, and interpersonal skills.
  • Independent project directorship experience.
Preferred Qualifications
  • Master of Science in analytical chemistry, the plant protection sciences (Plant Pathology, Weed Science, Entomology), horticulture, or related areas.
  • At least 3 years of experience in applied pest management research/regulatory sciences; or Bachelor of Science degree and at least 10 years' experience in chemistry or the applied pest management research/regulatory sciences.
  • Documented training and experience with U.S. Environmental Protection Agency Good Laboratory Practice Regulations.
Required License(s) or Certification(s)
  • NC Driver's license or the ability to obtain within 60 days of start.
Valid NC Driver's License required Yes Commercial Driver's License required No
Recruitment Dates and Special Instructions
Job Open Date 07/23/2026 Anticipated Close Date Open until filled Special Instructions to Applicants
Applicant required documents: Cover Letter, Resume/CV, and Contact Information for at least 3 Professional References.
Position Details
Position Number 00112207 Position Type EPS/SAAO Full Time Equivalent (FTE) (1.0 = 40 hours/week) 1.00 Appointment 12 Month Recurring Mandatory Designation - Adverse Weather Non Mandatory - Adverse Weather Mandatory Designation - Emergency Events Non Mandatory - Emergency Event Department ID 110313 - IR-4 Project EEO
NC State University is an equal opportunity employer. All qualified applicants will receive equal opportunities for employment without regard to age, color, disability, gender identity, genetic information, national origin, race, religion, sex (including pregnancy), sexual orientation, and veteran status. The University encourages all qualified applicants, including protected veterans and individuals with disabilities, to apply. Individuals with disabilities requiring disability-related accommodations in the application and interview process are welcome to contact 919-513-0574 to speak with a representative of the Office of Equal Opportunity.
If you have general questions about the application process, you may contact Human Resources at (919) 515-2135 or workatncstate@ncsu.edu.
Final candidates are subject to criminal & sex offender background checks. Some vacancies also require credit or motor vehicle checks. Degree(s) must be obtained prior to start date in order to meet qualifications and receive credit.
NC State University participates in E-Verify. Federal law requires all employers to verify the identity and employment eligibility of all persons hired to work in the United States.

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About North Carolina State University

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North Carolina State University (NCSU), located in Raleigh, NC, US, is a leading educational institution with a strong emphasis on research, academics, and public service. Established in 1887, NCSU operates in the education industry and endeavors to foster student success, and promote economic development by providing high-quality, affordable education, and conducting groundbreaking research across a variety of disciplines. With more than 100 majors, its academic offerings range from undergraduates to postgraduates along with doctoral studies - in various fields like engineering, natural resources, humanities, and social sciences. NCSU is firmly anchored on the core values of respect, responsibility, integrity, and innovation. Its mission is to create economic, societal, and intellectual prosperity for the people of North Carolina and the nation.

Industry

Colleges, universities, and professional schools

Company size

5,001 - 10,000 Employees

Headquarters location

Raleigh, NC, US

Year founded

1887

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