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Study Director Jobs (NOW HIRING)

The Study Director has overall responsibility for the technical conduct of all assigned tests as well as for the review, interpretation, analysis, documentation, and reporting of results. The study ...

Works with study sponsors to create study protocols * Informs Live Phase Study Coordinator of decisions to initiate studies and thereby proceed with ordering animals and necessary study supplies

Argenta is currently looking to fill the role of Study Director at our Oakland, NE location. Key Responsibilities * Approve and sign study protocol * Ensure objectives meet regulatory requirements

About The Role Works under the guidance of designated Study Director(s), Contributing Scientists and Principal Investigators, as appropriate, to provide administrative and professional support for ...

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Assists Study Directors on select projects under the direction and review of the Study Director team. Assists in collection, documentation and analysis of pre-clinical data. Assists in the ...

Support the Study Director in developing study protocols, amendments, and related documentation. * Facilitate cross-functional communication, establish and track study timelines, and prepare/lead ...

Argenta is currently looking to fill the role of Study Director at our Oakland, NE location. Key Responsibilities * Approve and sign study protocol * Ensure objectives meet regulatory requirements

Argenta is currently looking to fill the role of Study Director at our Oakland, NE location. Key Responsibilities * Approve and sign study protocol * Ensure objectives meet regulatory requirements

Support the Study Director in developing study protocols, amendments, and related documentation. * Facilitate cross-functional communication, establish and track study timelines, and prepare/lead ...

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Study Director information

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$45K

$128.4K

$232.5K

How much do study director jobs pay per year?

As of Jul 16, 2026, the average yearly pay for study director in the United States is $128,367.00, according to ZipRecruiter salary data. Most workers in this role earn between $58,000.00 and $188,500.00 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 cities are hiring for Study Director jobs? Cities with the most Study Director job openings:
What are the most commonly searched types of Study jobs? The most popular types of Study jobs are:
Who are the top companies hiring for Study Director jobs? The top employers for Study Director jobs are:
What states have the most Study Director jobs? States with the most job openings for Study Director jobs include:
Infographic showing various Study Director job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, 1% Temporary, and 1% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $128,367 per year, or $61.7 per hour.
Study Director I or II

Study Director I or II

Sotera Health

Nelson, NE • On-site

Full-time

Re-posted 6 days ago


Job description

The name Sotera Health was inspired by Soteria, the Greek goddess of safety, and reflects the Company's unwavering commitment to its mission, Safeguarding Global Health.

Sotera Health Company is a leading global provider of mission-critical sterilization and lab testing and advisory services for the healthcare industry. With a combined tenure across our businesses of nearly 200 years and our industry recognized scientific and technological expertise, we help to ensure the safety of millions of patients and healthcare practitioners around the world every year.

Across our 64 facilities worldwide, we have over 3,000 employees who are dedicated to safety and quality. We are a trusted partner to more than 5,800 customers in over 50 countries, including more than 40 of the top 50 medical device companies and 9 of the top 10 pharmaceutical companies.

Job Summary:

The Study Director has overall responsibility for the technical conduct of all assigned tests as well as for the review, interpretation, analysis, documentation, and reporting of results. The study director is the single point of study control. The study director ensures all assigned studies are completed on time.

Essential Duties:
Scientific/General

  • Ensure reports are compliant with current procedures.
  • Ensure final reports accurately reflect the data, results, and conclusions of the testing.
  • Act as a final signature for assigned studies.
  • Collaborate on Customer Specification Sheets (CSS) etc. as assigned.
  • Ensure sample and data traceability are maintained throughout testing.
  • Ensure calculations and statistics accurately reflect the raw data.
  • Ensure accuracy of raw data.
  • Ensure test controls and monitors are accurately recorded and reviewed.
  • Collaborate within the Quality Event (QE) process.
  • Read and maintain an understanding of validation procedures.
  • Collaborate with document owners on Standard Test Procedures (STP) as assigned.

Regulatory Compliance

  • Know and follow applicable regulatory requirements (GMP, GLP, ISO, etc.).
  • Know and follow company policies and procedures.
  • Ensure that test procedures are approved, communicated to, and followed by analysts.
  • Ensure all data are accurately and concurrently recorded.
  • Ensure unforeseen circumstances or events are recorded and that corrective action is taken.
  • Complete required training on time.

Customer Service

  • Uphold the NL service standard.
  • Communicate regularly with sponsors as needed to relay study updates and CSS details.
  • Meet or exceed sponsor expectations.
  • Collaborate with the Sales department on testing quotes.
  • Maintain a general understanding of company pricing and credit policies.
  • Review and update study information in CRM and/or other laboratory systems.

Project Management

  • Coordinate workflow to ensure sponsor expectations are met.

Professionalism

  • Keep current with technical and scientific information.
  • Ensure analysts understand testing performed on behalf of the study director.
  • Attend work regularly and reliably.
  • Adhere to all policies and procedures.
  • Perform other duties as assigned

Competencies of this position
Technical

  • Knowledge of laboratory testing, equipment, procedures, and basic math sufficient to direct and oversee assigned testing.
  • Ability to follow written procedures.
  • Good documentation practice (GDP).
  • Effective critical thinking, problem-solving, and decision-making skills.
  • Ability to learn and comprehend difficult tasks.
  • Ability to troubleshoot problems.
  • Attention to detail.
  • Effective computer skills: Microsoft Office and laboratory systems.

Values

  • Ability to work in a team environment, including the ability to give and receive feedback.
  • High standards of honesty, integrity, and quality.
  • Willingness to identify and communicate process improvement ideas.
  • Customer-focused attitude.
  • Strong work ethic and initiative.

Professional

  • Effective communication skills: verbal, written, and active listening.
  • Ability to organize and manage workload.
  • Ability to meet deadlines

Work Environment:

This job operates in a professional laboratory environment. This role routinely uses standard office equipment and lab equipment including but not limited to computers keyboards, computer mouse, telephones, photocopiers, file cabinets, microscopes, micropipettes, pipette aids, various hand tools, and analytical equipment.
The possibility exists for exposure to biological and chemical hazards, exposure to carcinogenic compounds and other environmental aspects which may be considered unfavorable. Employees are expected to follow Biosafety and Chemical Hygiene policies, practices and procedures.
Travel:
Occasional local travel during the business day and occasional out of the area or overnight travel may be expected.

Physical requirements:
The physical demands described here are a representative of those that must be met to perform the essential job functions.

  • Requirements to stand and traverse to various office and lab locations and sit at a computer workstation will vary.
  • Bending, stooping, and crouching.
  • Occasional push and pull tasks with one or both hands.
  • Must be able to work while wearing personal protective equipment such as safety glasses, goggles, face shields, gloves, lab coats and personal protective equipment deemed necessary to protect testing and to protect employees from various solutions, wastes, etc.
  • Must be able to lift up to 45lbs.

Education and experience requirements:

  • B.S. degree (life science strongly preferred) or
  • A.A./A.S. or equivalent* and two years NL laboratory experience*, or
  • High School diploma or GED, five years NL laboratory experience* in addition to demonstrate proficiency for test coordination.
  • Successful completion of Study Director Training.

Sotera Health goes to market through its three best-in-class businesses - Sterigenics, Nordion and Nelson Labs. Sterigenics is a leading global provider of outsourced terminal sterilization and irradiation services for the medical device, pharmaceutical, food safety and advanced applications markets. Nordion is the leading global provider of Co-60 and gamma irradiators, which are key components to the gamma sterilization process. Nelson Labs is a global leader in outsourced microbiological and analytical chemistry testing and advisory services for the medical device and pharmaceutical industries.