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Study Director Jobs in Basking Ridge, NJ (NOW HIRING)

Eurofins

Study Director

New Brunswick, NJ · On-site

Supervise study conduct. * Assist in protocol development, design and implementation. * Responsibilities as stated in GLP regulations. * Data interpretation and report writing. * Client liaison.

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$46.4K

$132.3K

$239.6K

How much do study director jobs pay per year?

As of Sep 7, 2026, the average yearly pay for study director in Basking Ridge, NJ is $132,290.00, according to ZipRecruiter salary data. Most workers in this role earn between $59,800.00 and $194,300.00 per year, depending on experience, location, and employer.

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.

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.

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 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.

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.

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Study Director jobs near you

Study Director

Eurofins Scientific

South Brunswick, NJ • On-site

Full-time

Re-posted yesterday

Eurofins rating

7.5

Company rating: 7.5 out of 10

Based on 181 frontline employees who took The Breakroom Quiz

64th of 121 rated laboratories

Job description

Company Description

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labeling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

Job Description

Supervise and assist in the conduct of regulatory studies performed.  Responsibilities include:

  • Supervise study conduct.
  • Assist in protocol development, design and implementation.
  • Responsibilities as stated in GLP regulations.
  • Data interpretation and report writing.
  • Client liaison.

Management Responsibilities:

  • Overall, day-to-day laboratory operation including supervision of technical staff assigned to your studies.
  • Scheduling and coordinating initiation and conduct of studies.
  • Ensure that the study schedule and financial aspects of each study that you are responsible for are accurately tracked on a regular basis.

Technical Responsibilities: 

Overall responsibility for the technical conduct of all studies and interpretation, analysis, documentation and reporting of results.  Specifically:

  • Establish test protocols and corresponding SOP's.
  • Develop experimental design and supervise implementation of experiments (tests).
  • Obtain sponsor approval of protocols and institute any necessary deviations from the test protocol with sponsor approval.
  • Ensure all experimental data is properly recorded and that observations of unanticipated responses of the test system are accurately recorded and verified.
  • Ensure tests are conducted in accordance with the test protocol and SOP.
  • Supervise conduct of all phases of the study, including participation in study conduct.
  • Ensure that GLP regulations are followed.
  • Interpretation, calculation, analysis, documentation and reporting of results.
  • Instruct, train and supervise scientists in all procedures.
  • Maintain liaison with sponsors, advising them of test results; and assisting with protocol development.
  • Maintain liaison with regulatory agencies in conjunction with: test protocols, and past or present studies submitted for regulatory approval, compliance with GLP's and appropriate test guidelines.
  • Ability to safely wear a respirator required
Qualifications
  • BS degree in a field related to their area of responsibility (e.g. animal science, chemistry, biology, microbiology).
  • Minimum of 5 years experience overseeing biocompatibility studies
  • Intimate working familiarity and/or ability to quickly learn and develop such familiarity with all government regulations dealing with testing particularly EPA, FDA, DOT, OECD, and GLP regulations in addition to ISO standards.
  • Hands-on working knowledge of the tests that will be under their responsibility.
  • Good administrative skills and leadership ability.  Must communicate effectively and write well.
Additional Information

Position is full-time, Monday-Friday, 9:00am.- 5:00 pm, with overtime as needed.  Candidates currently living within a commutable distance of Dayton, NJ are encouraged to apply.

Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

What Eurofins employees say

Pay

Benefits

Hours and flexibility

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About Eurofins

Sourced by ZipRecruiter

Industry

Scientific research and development services, biotechnology research and development and environmental consulting services

Company size

10,000+ Employees

Headquarters location

Leacock, PA, US

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