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Study Director Jobs in Washington (NOW HIRING)

Director, Toxicology

Gaithersburg, MD · On-site

$120.20 - $175K/hr

Assigns personnel to specific studies/projects. * Reviews weekly workload of assigned study directors. * Conducts protocol and report peer reviews. * Reviews study protocols. * Approves ...

Director, Toxicology

Gaithersburg, MD · On-site

$120.20 - $175K/hr

Assigns personnel to specific studies/projects. * Reviews weekly workload of assigned study directors. * Conducts protocol and report peer reviews. * Reviews study protocols. * Approves ...

Director, Toxicology

Gaithersburg, MD · On-site

$120.20 - $175K/hr

Assigns personnel to specific studies/projects. * Reviews weekly workload of assigned study directors. * Conducts protocol and report peer reviews. * Reviews study protocols. * Approves ...

The Director for Evidence Synthesis will be a critical member of the Science Knowledge and Expertise (SKE) unit within the APA Psychology Team. SKE staff support the use and dissemination of rigorous ...

Study Coordinator

Washington, DC · On-site

$50K - $60K/yr

Report to the Project Director and the Principal Investigator regarding assignments and duties ... Course study concentration in a health-related field is desirable. Compliance Salary Range ...

Report to the Project Director and the Principal Investigator regarding assignments and duties ... Course study concentration in a health-related field isdesirable. Compliance Salary Range ...

Study Director must fulfill all aspects of the role, as outlined in the GLP regulations * Maintains overall scientific responsibility for the study design, interpretation, and reporting of study ...

Quality Assurance Auditor I

Gaithersburg, MD · On-site

$26.44 - $36.20/hr

Support and participate in company initiatives as directed * Maintain thorough knowledge of facility SOPs, policies, study protocols, etc. * Adhere to all safety regulations and procedures * Provide ...

Support and participate in company initiatives as directed * Maintain thorough knowledge of facility SOPs, policies, study protocols, etc. * Adhere to all safety regulations and procedures * Provide ...

Study Director must fulfill all aspects of the role, as outlined in the GLP regulations * Maintains overall scientific responsibility for the study design, interpretation, and reporting of study ...

Study Director must fulfill all aspects of the role, as outlined in the GLP regulations * Maintains overall scientific responsibility for the study design, interpretation, and reporting of study ...

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Showing results 1-20

Study Director information

See Washington salary details

$51K

$145.4K

$263.3K

How much do study director jobs pay per year?

As of Jul 16, 2026, the average yearly pay for study director in Washington is $145,388.00, according to ZipRecruiter salary data. Most workers in this role earn between $65,700.00 and $213,500.00 per year, depending on experience, location, and employer.

What is the highest paying job in research?

In research, senior roles such as Principal Investigator, Research Director, or Chief Scientific Officer tend to be the highest paying, often earning six-figure salaries. These positions typically require advanced degrees, extensive experience, and leadership skills in specialized fields like pharmaceuticals, biotechnology, or data science.

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 Is the Job of a Study Director?

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 to become a study director?

To become a study director, typically a candidate needs a bachelor's degree in a scientific field such as biology, chemistry, or related disciplines, along with several years of experience in laboratory or research settings. Advanced roles often require a master's or doctoral degree and knowledge of Good Laboratory Practices (GLP) and regulatory requirements. Developing strong project management, leadership skills, and familiarity with relevant testing methods are also important for this role.

How much do research directors make in the US?

Research directors, including study directors in research settings, typically earn a median annual salary of around $80,000 to $120,000 in the US, depending on experience, industry, and location. They often require advanced degrees and strong project management skills to oversee research projects effectively.

What are the key skills and qualifications needed to thrive as a Study Director, and why are they important?

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 role of a study director?

A study director is responsible for designing, planning, and overseeing scientific studies, ensuring they comply with regulatory standards such as Good Laboratory Practice (GLP). They coordinate research activities, analyze data, and prepare reports to support product development or safety assessments.
What are the most commonly searched types of Study jobs in Washington? The most popular types of Study jobs in Washington are:
What are popular job titles related to Study Director jobs in Washington? For Study Director jobs in Washington, the most frequently searched job titles are:
What cities in Washington are hiring for Study Director jobs? Cities in Washington with the most Study Director job openings:
Infographic showing various Study Director job openings in Washington as of July 2026, with employment types broken down into 1% As Needed, 80% Full Time, 17% Part Time, 1% Temporary, and 1% Contract. Highlights an 90% Physical, 5% Hybrid, and 5% Remote job distribution, with an average salary of $145,388 per year, or $69.9 per hour.
Director, Toxicology

Director, Toxicology

Inotiv

Gaithersburg, MD • On-site

$120.20 - $175K/hr

Full-time

Medical, Dental, Retirement, PTO

Posted 23 days ago


Inotiv rating

8.2

Company rating: 8.2 out of 10

Based on 21 frontline employees who took The Breakroom Quiz

24th of 59 rated research


Job description

The Director of Toxicology is the scientific leader for the site and serves as a mentor and manager for a group of Study Directors overseeing general toxicology and safety pharmacology studies. As a group manager the Director will be responsible for reviewing protocols, SOPs, data, and reports, as well as distributing the workload appropriately within the team. The Director will be responsible for representing Inotiv in meetings with clients as a subject matter expert to communicate capabilities and experience. The Director will also work closely with the corporate Executive Director of Toxicology to ensure harmonization of deliverables to our clients across multiple sites and lead as an agent of change management when necessary.
Corporate Responsibilities:
  • Adherence to laboratory health and safety procedures
  • Adherence to Standard Operating Procedures (SOPs)
  • Adherence to applicable company policies and guidelines
  • Adherence to federal and/or local regulations as applicable
  • Proficient in the duties of a Senior Study Director.
  • Supervises assigned Study Directors as follows:
    • Assigns personnel to specific studies/projects.
    • Reviews weekly workload of assigned study directors.
    • Conducts protocol and report peer reviews.
    • Reviews study protocols.
    • Approves interpretation of study data and final reports prepared by other study directors.
    • Oversees and assists personnel in job performance.
    • Coordinates training and professional development of assigned personnel.
    • Performs performance management of direct reports performance evaluations, training, hiring and dismissal decisions and time sheet approval.
  • Perform job functions in accordance with departmental and corporate mission.
  • May serve as a Study Director and/or in a technical capacity in area of expertise, i.e. General Toxicology.
  • Recognizes potential training needs in preparation for new business/techniques and coordinates with appropriate staff to assure training is implemented.
  • Reviews and develops new procedures, technologies, and SOPs as required.
  • Serves as a professional resource to other departments.
  • May prepare manuscripts and/or present at scientific meetings.
  • Serves as an expert resource to the business development staff during in the preparation of proposals.

Additional Requirements:
  • Ability to accurately interpret and communicate scientific and organizational information with internal and external clients.
  • Ability to effectively interact with clients and regulatory personnel.
  • Ability to produce high quality data while working under the pressure of strict deadlines.
  • Weekend and holiday work as required.
  • Work requires entrance into the Vivarium areas. Demonstrated immunological tolerance as necessary to be present in animal areas.
  • Work requires passing annual physical and the use of other PPE (personal protective equipment)

Professional Responsibilities:
  • Attends continuing education courses, as appropriate.
  • Maintain an active involvement in professional toxicology organizations.
  • Be knowledgeable in regulatory requirements.
  • Other special projects and duties as assigned.

Minimum Requirements:
Education:
  • Doctoral degree and D.A.B.T. certification required.
  • Five years' experience in general toxicology, pharmacology and/or related field.

Experience:
  • Excellent skills in basic computer applications such as email, MS Word, Excel and Power Point.
  • Excellent oral and written communication skills.
  • Experience managing a team is preferred.
  • Previous publications preferred.
  • Able to work independently and participate in multiple pre-clinical research studies concurrently.

Working Conditions/Physical Requirement
  • Extended computer and display screen equipment usage
  • Ability to push, pull, lift pounds unassisted.
  • Stand / walk for extended period of time.
  • Fine manipulation including handle touch object or tools and ability to handled controls to perform work.
  • Ability to read and interpret materials, verbally communicate, and hear required.

The anticipated base salary for this position could range from between $120.200 to $175,000 and will depend, in part, on the successful candidate's qualifications for the role, including education and experience.
Benefits include health and dental coverage, short- and long-term disability, paid time off, 401K participation with company match, etc.
Inotiv is a proud equal opportunity employer and an E-Verify employer.
#LI-JM1
#LI-Onsite
*This position could be offered at different levels for candidates who qualify with a combination of advanced levels of education and/or years of experience. The salary range will adjust along with the level of the role to match the person's relevant experience and/or education level.
Inotiv is a growing contemporary drug discovery and development company where we "Play to Win" in an industry rich with opportunity. Together, we face challenges and together we win in the delivery of world-class drug discovery and development solutions that impact the health and well-being of people all over the world. There's an opportunity for everyone at all phases of a career, each individual's unique skill set has an impact on the work we conduct. If you have the talent and desire to impact the quality of people's lives, we have the career opportunities to make it happen. Join us in embracing research and science to impact the health and well-being of people all over the world.
Salary will be commensurate with experience and responsibilities. Benefits include health and dental coverage, short- and long-term disability, paid time off, paid parental leave, 401K, and more!
Inotiv is an Equal Opportunity Employer. It is our policy to provide a fair and equal employment opportunity to all persons, regardless of age, race, color, religion, sex, gender, gender identity, gender expression, sexual orientation, genetic information, disability, national origin, veteran status, or any other basis prohibited by law. This policy governs all aspects of employment, including selection, job assignment, compensation, discipline, termination and access to benefits and training.

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About Inotiv

Sourced by ZipRecruiter

Industry

Scientific research and development services

Company size

201 - 500 Employees

Headquarters location

West Lafayette, IN, US

Year founded

1974

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