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Study Director Jobs (NOW HIRING)

Altasciences

Study Coordinator I

Olyphant, PA · On-site

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 ...

Altasciences

Study Coordinator I

Olyphant, PA · On-site

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 ...

Argenta

Study Director - Americas CRO

Oakland, NE · On-site

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

NAMSA

Study Coordinator

Northwood, OH · On-site

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 ...

Argenta

Study Director - Americas CRO

Oakland, NE · On-site

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

Study Director - Americas CRO

Oakland, NE · On-site

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

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 ...

Altasciences

Scientist, Study Director

Everett, WA

$79K - $120K/yr

Performs functions of a Study Director with a full SD workload, including GLP studies. * Functions as an independent Study Director with overall responsibility for the technical conduct of assigned ...

New

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 Aug 6, 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 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.
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Study Director jobs near you
Infographic showing various Study Director job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 84% Full Time, 12% Part Time, 1% Temporary, and 2% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $128,367 per year, or $61.7 per hour.

Study Coordinator I

Altasciences

Olyphant, PA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 24 days ago

Altasciences rating

7.6

Company rating: 7.6 out of 10

Based on 17 frontline employees who took The Breakroom Quiz

60th of 120 rated laboratories

Job description

Your New Company!
At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences.
We are better together and together We Are Altasciences.
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 accurate study progression based on Protocols and Method Validation Plans, organization, scheduling, reporting, client relations and operations.
What You'll Do Here
  • Assist with the preparation and distribution of Protocols, Analytical Study Plans and Amendments/Amended Protocols.
  • Schedule and/or help conduct Protocol review meetings with Study Director guidance.
  • Create study schedules for data collection within the electronic data capture system and implement schedule changes as a result of Protocol Amendments/Amended Protocols, as necessary.
  • Draft and edit Project Review Forms (PRF) with Study Director guidance.
  • Assist with preparation and maintenance of study notebooks, study forms, and other necessary materials for studies.
  • Support the Study Director or Principal Investigator with the planning and hosting of client visits.
  • Review raw data throughout the life of a study for clerical/technical errors, thoroughness and consistency, and adherence to SOPs, Protocol specifications and compliance with Good Laboratory Practices (GLPs), as appropriate.
  • Coordinate correction of raw data with appropriate staff.
  • Report any deviations to the Study Director.
  • Coordinate study activities related to audits.
  • Perform data verification as needed.
  • Generate data tables for inclusion in reports based on requirements
  • Assist in the preparation of the report(s) (e.g. drafting the Materials and Methods section), utilizing the appropriate report template.
  • Collect and collate report components for the final report under the supervision of the
  • Study Director utilizing electronic publishing tools.
  • Provide assistance with archiving and preparation of studies for finalization.
  • Support the Study Director(s), Contributing Scientists and Principal Investigators with the monitoring, tracking and communication of study milestones throughout departments.
  • Provide coordination for both non-GLP studies and GLP studies from study initiation to finalization under the guidance of the Study Director.

What You'll Need to Succeed
  • A Bachelor degree or college coursework in a scientific discipline and relevant experience may substitute for the educational requirement.
  • Mimimum of 1 year experience in a scientific environment or an equivalent combination of education and experience.
  • General to advanced computer skills: proficiency working with MS Word, Excel and Adobe Acrobat.
  • Excellent verbal and written communication skills
  • Working knowledge of descriptive statistics.

What We Offer
Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.
Altasciences' Benefits Package Includes
  • Health/Dental/Vision Insurance Plans
  • 401(k)/RRSP with Employer Match
  • Paid Vacation and Holidays
  • Paid Sick and Bereavement Leave
  • Employee Assistance & Telehealth Programs
  • Telework when applicable

Altasciences' Incentive Programs Include
  • Training & Development Programs
  • Employee Referral Bonus

#LI-TN1
MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH
Altasciences is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability or any other protected grounds under applicable legislation. Reasonable accommodations for persons with disabilities during the recruitment process are available upon request. Join us at Altasciences!

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