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Study Director Jobs (NOW HIRING)

Inotivco

Study Director II

Alice, TX · On-site

This position is responsible for the execution of studies as assigned by in-life management including managing study resources, activities, and operations. This position will be responsible for all ...

Inotiv

Study Director II

Alice, TX · On-site

This position is responsible for the execution of studies as assigned by in-life management including managing study resources, activities, and operations. This position will be responsible for all ...

Sotera Health

Study Director I or II

Nelson, NE · On-site

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 ...

Neuralink

Preclinical Study Coordinator

Austin, TX

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

Neuralink

Preclinical Study Coordinator

Austin, TX · On-site

$31 - $53/hr

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

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 ...

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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 Jun 25, 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 jobs pay $10,000 a month without a degree?

A Study Director typically requires specialized education or experience and may not reach $10,000 a month without a degree. However, some high-paying roles in sales, real estate, or entrepreneurship can earn $10,000 or more monthly without formal degrees, often relying on skills, certifications, or business acumen. These roles usually demand strong communication, self-motivation, and industry knowledge.

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 jobs pay 2000 a day?

Study Directors in specialized research fields or senior project managers in high-stakes industries can earn around $2,000 per day, especially with extensive experience, advanced certifications, and leadership responsibilities. Such roles often require advanced degrees, strong project management skills, and the ability to oversee complex projects or clinical trials, typically working in regulated or high-demand environments.

What jobs pay 500,000 a year in the US?

In the US, high-paying roles such as senior executives, specialized surgeons, and certain investment bankers can earn $500,000 or more annually. Study Directors in the biotech or pharmaceutical industries may reach this level with extensive experience, leadership responsibilities, and advanced expertise, especially in large organizations or with bonuses and profit sharing included.

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.

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 oversees the planning, execution, and reporting of scientific studies, ensuring they comply with regulatory standards such as Good Laboratory Practice (GLP). They coordinate research activities, manage study teams, and review data to ensure accuracy and integrity throughout the study process.
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Study Director jobs near you
Study Director: Translational Oncology

Study Director: Translational Oncology

Certis Oncology Solutions, Inc.

San Diego, CA • On-site

$90K - $120K/yr

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

Description:


Certis is seeking a highly motivated and self-directed, Study Director that will:

· Design, administer and interpret client-sponsored studies, serving as the primary scientific and operational liaison

· Evaluate and integrate innovative technologies and methodologies that enhance translational relevance and accelerate therapeutic insights

· Foster a collaborative environment by modeling strong scientific communication, proactive coordination, and high-quality study execution

· Report to the Sr. Director of Scientific Operations for guidance on study milestones, financial approvals, and client strategy


· Develop, amend, and oversee study protocols and related documentation to ensure clarity, compliance, and alignment with client objectives

· Serve as the primary point of contact for internal and external study communications, providing consistent updates and guidance throughout the project lifecycle

· Monitor multiple complex in vitro, ex vivo and in vivo studies by managing daily tasks schedules, data integrity, and resolution of study discrepancies

· Calculate dosing regimens and formulations

· Analyze and interpret study data with scientific rigor, preparing interim and final deliverables that highlight key insights and outcomes

· Support the logistics and record keeping of sample shipments

· Track study financial actuals, prepare costing reports, and support invoicing activities

· Contribute to Certis’ scientific growth by researching, evaluating, and recommending new models, technologies, or partnerships that advance precision oncology and translational research

Requirements:
  • Ph.D. in Life Science related field preferred, MS required
  • 3 years experience in managing oncology-related assays, and/or in-vivo immunology, pharmacology or related scientific studies
  • Experience preparing study protocols, amendments, and reports for studies.
  • Proficient in Microsoft Office Suite (Word, Powerpoint, Outlook) and StudyLog
  • Experience working with laboratory information systems/electronic notebooks
  • Experience in managing multiple projects and communications
  • Experience in a CLIA-certified environment preferred
  • Experience with IND preparation and submissions preferred
  • Direct management experience preferred
  • Vivarium experience preferred
  • Strong orientation to inclusive teamwork, attention to detail
  • Effective communication skills for a variety of stakeholders