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Associate Study Director Jobs (NOW HIRING)

Reporting to the Program Director, Master of Science in Physician Associate Studies, the Principal Faculty/Assistant Professor of Physician Associate Studies is responsible for course development ...

Animal Research Technician

Olyphant, PA · On-site

$16.25 - $22.25/hr

About the Role Research Associate I will perform technical procedures, restrain animals, operate ... Support study supervisor(s) and study director(s) by performing and assisting with sample and data ...

R&D Technician

North Chicago, IL · On-site

$17.25 - $23.75/hr

The position of the R&D Technician requires individuals to work with Study Directors, associate Toxicologists, Clinical Veterinarians and Study Pathologists in conducting non-clinical laboratory ...

Animal Research Technician

Olyphant, PA

$16.25 - $22.25/hr

About the Role Research Associate I will perform technical procedures, restrain animals, operate ... Support study supervisor(s) and study director(s) by performing and assisting with sample and data ...

Job Title Program Director of the Physician Associates Program Department Dean's Office College of ... The Physician Associate Studies Program at Miami University is a 27-month, master-level curriculum.

Vivarium Technician

Exton, PA · On-site

$15.25 - $20.50/hr

Vivarium Manager / Study Director Position Summary: We are seeking a reliable and detail-oriented ... Associate's or Bachelor's degree in Animal Science, Biology, or a related field preferred. * ALAT ...

Apply Early

Local Study Associate Director - FSP

$34.25 - $46.75/hr

The Local Study Associate Director (LSAD) leads Local Study Team(s) (LSTs) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines ...

Local Study Associate Director - FSP

$34.25 - $46.75/hr

The Local Study Associate Director (LSAD) leads Local Study Team(s) (LSTs) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines ...

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Associate Study Director information

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$30.5K

$102.7K

$173K

How much do associate study director jobs pay per year?

As of Jul 4, 2026, the average yearly pay for associate study director in the United States is $102,728.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,000.00 and $141,000.00 per year, depending on experience, location, and employer.

What are some common challenges faced by an Associate Study Director, and how can they be addressed?

Associate Study Directors often face challenges such as managing multiple studies simultaneously, ensuring regulatory compliance, and coordinating communication between cross-functional teams. Balancing strict timelines with high-quality data collection requires strong organizational skills and attention to detail. To address these challenges, it's essential to develop robust project management habits, maintain clear documentation, and foster open communication with both internal teams and external stakeholders. Regular training on regulatory requirements and effective use of study management tools can also greatly enhance efficiency and accuracy in the role.

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

To thrive as an Associate Study Director, you need a solid background in life sciences, data analysis, and project management, typically supported by a relevant degree such as biology or pharmacology. Familiarity with laboratory information management systems (LIMS), regulatory guidelines (GLP/GCP), and data reporting tools is crucial. Strong organizational skills, attention to detail, and effective communication are standout soft skills for this role. These competencies ensure studies are conducted accurately, regulatory requirements are met, and projects are delivered on time.

What is the difference between Associate Study Director vs Study Director?

AspectAssociate Study DirectorStudy Director
CredentialsTypically requires a bachelor's or master's degree in a related field, with some experience in study managementRequires a higher level of education (often a master's or PhD) and extensive experience in study oversight
Work EnvironmentSupports study planning and execution under supervision, often in laboratory or research settingsLeads and oversees entire studies, ensuring compliance and data integrity
Employer & Industry UsageCommonly employed in contract research organizations (CROs) and laboratoriesUsed in similar settings but with greater responsibility and authority

The main difference between an Associate Study Director and a Study Director lies in their level of responsibility and experience. Associate Study Directors support study activities and assist in management tasks, while Study Directors lead and oversee the entire study process, ensuring compliance and quality. Both roles are essential in research and testing environments, with the Study Director holding a more senior position.

What are Associate Study Directors?

Associate Study Directors are professionals who assist in the planning, coordination, and management of scientific studies, often within research or laboratory settings. They work under the guidance of a Study Director to ensure studies are conducted according to protocols, regulatory requirements, and quality standards. Their responsibilities may include overseeing data collection, ensuring compliance with Good Laboratory Practices (GLP), managing study documentation, and communicating with clients or sponsors. This role is essential in maintaining the integrity and accuracy of research projects, particularly in fields such as pharmaceuticals, environmental science, and toxicology.
More about Associate Study Director jobs
What cities are hiring for Associate Study Director jobs? Cities with the most Associate Study Director job openings:
What are the most commonly searched types of Study Director jobs? The most popular types of Study Director jobs are:
What states have the most Associate Study Director jobs? States with the most job openings for Associate Study Director jobs include:
Infographic showing various Associate Study Director job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 50% Full Time, 46% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $102,728 per year, or $49.4 per hour.
Senior Scientific Associate - Toxicology

Senior Scientific Associate - Toxicology

Charles River Laboratories, Inc.

Horsham, PA • On-site

$88K - $92K/yr

Other

Medical, Retirement, PTO

Posted 11 days ago


Charles River Laboratories rating

8.2

Company rating: 8.2 out of 10

Based on 91 frontline employees who took The Breakroom Quiz

29th of 73 rated pharmaceutical


Job description

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we'll help you build a career that you can feel passionate about.

Job Overview

Responsible for overseeing study conduct of preclinical efficacy and/or toxicology studies assigned by TFM within safety assessment. Responsible for protocols/study plans, coordinate with technical teams to allow appropriate execution of the study, including establishing study schedules, ensuring adequate Standard Operating Procedures are available and adhered to, oversees adequate data recording and reporting, and ensure regulatory requirements/expectations are met for the assigned study(ies).  Overall interpretation of preclinical toxicity studies, evaluation and preparation of reports from the data collected during these studies, communication with sponsor representatives, initiating contact with potential clients will be required, Familiarity with study costs and impact of changes will be required.  May be involved with development of new technologies/procedures.    

Job Description

ESSENTIAL DUTIES AND RESPONSIBILITIES:  

  • Function as an independent Study Director in accordance with the applicable Good Laboratory Practices (GLPs).
  • Designs, writes, reviews and edits, as necessary, Study Plans, amendments and study schedules that define and schedule all study activities.
  • Oversees and coordinates all aspects of study procedures, whether performed within the department or by service departments.
  • Ensures that projects are performed according to Standard Operating Procedures and Good Laboratory Practice regulations and is aware of appropriate regulations, guidelines and guidances.
  • Writes, reviews and edits, as necessary, draft or final reports that document all study related procedures and results.
  • Prompt verbal or written communication with Sponsors on study related business.
  • Understands regulations and GLP's as they relate to primary area of focus.
  • Understands the study process from proposal to report.
  • Oversees and coordinates study conduct (protocol development, technical guidance, and reporting).
  • Assists in study planning, scheduling, and execution under the supervision of Sr. Scientist(s)/Scientific Manager.
  • Host client visits and telephone/video conferences with support/guidance from Sr. Scientist(s) as needed.
  • Effectively communicates with internal and external clients in a manner that generates confidence and builds trust.
  • Works on studies/programs of basic complexity.
  • Basic knowledge of Quality Assurance (QA)/Quality Control (QC) process.
  • Experience handling laboratory animal data. Interacts with veterinary staff, understands the IACUC process, and understands the Study Director role in animal welfare. 
  • Gains familiarity with overall project costs and communicates with the technical supervisor as well as the Scientific Manager on issues of staffing and equipment.
  • May attend scientific meetings, conferences and training courses to enhance job and professional skills.

The pay range for this position is between $88,000- 92,000/yr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Qualifications

QUALIFICATIONS:
Education:  Minimum of a Bachelor's degree (BA/BS) or equivalent in Toxicology, Pharmacology, or related discipline.  Prefer Master's (MA/MS), Doctorate (PhD), PharmD, DVM, or MD degree or equivalent. Five years' minimum relevant work experience is required for consideration. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.

About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market.  Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.


About Charles River
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.

With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.

At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

We're committed to providing benefits that elevate your quality of life.  Based on your position these may include:  bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

For more information, please visit www.criver.com.


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About Charles River

Sourced by ZipRecruiter

Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 20,000 employees within 110 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

Wilmington, MA, US

Year founded

1947