ZipRecruiter

Log In

1

Study Director Jobs in Edison, NJ (NOW HIRING)

WuXi AppTec

Scientist III

Cranbury, NJ · On-site

$90K - $110K/yr

Functions as a study director, principal investigator, or project coordinator, responsibilities include serving as a primary contact for sponsors, planning, supervising and exacting complex ADME ...

WuXi AppTec

Scientist III

Cranbury, NJ · On-site

$90K - $110K/yr

Functions as a study director, principal investigator, or project coordinator, responsibilities include serving as a primary contact for sponsors, planning, supervising and exacting complex ADME ...

WuXi AppTec

Scientist III

Cranbury, NJ

$90K - $110K/yr

Functions as a study director, principal investigator, or project coordinator, responsibilities include serving as a primary contact for sponsors, planning, supervising and exacting complex ADME ...

WuXi AppTec

Senior Scientist I, Bioanalytical

Cranbury, NJ · On-site

$93K - $127K/yr

Functions as a study director, principle investigator, or project coordinator including serving as a primary contact for sponsors, responsibilities include planning and supervising more complex and ...

WuXi AppTec

Senior Scientist I, Bioanalytical

Cranbury, NJ · On-site

$93K - $127K/yr

Functions as a study director, principle investigator, or project coordinator including serving as a primary contact for sponsors, responsibilities include planning and supervising more complex and ...

IQVIA

Senior Global Clinical Study Manager

New York, NY · On-site

Required Experience * 2+ years of global study management experience * Experience across multiple ... Make a direct impact on patient outcomes worldwide IQVIA is a leading global provider of clinical ...

WuXi AppTec

Senior Scientist I, Bioanalytical

Cranbury, NJ · On-site

$93K - $127K/yr

Functions as a study director, principle investigator, or project coordinator including serving as a primary contact for sponsors, responsibilities include planning and supervising more complex and ...

WuXi AppTec

Senior Scientist I

Cranbury, NJ

$100K/yr

Function as a study director, principal investigator, or project manager including serving as a primary contact for projects, responsibilities include planning, conducting and delivering projects in ...

WuXi AppTec

Senior Scientist I

Cranbury, NJ · On-site

$100K/yr

Function as a study director, principal investigator, or project manager including serving as a primary contact for projects, responsibilities include planning, conducting and delivering projects in ...

next page

Showing results 1-20

All JobsStudy JobsStudy Director JobsStudy Director Jobs in Edison, NJ

Study Director information

See Edison, NJ salary details

$46.6K

$132.9K

$240.7K

How much do study director jobs pay per year?

As of Jul 27, 2026, the average yearly pay for study director in Edison, NJ is $132,893.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,000.00 and $195,100.00 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.
More about Study Director jobs
What are the most commonly searched types of Study jobs in Edison, NJ? The most popular types of Study jobs in Edison, NJ are:
What job categories do people searching Study Director jobs in Edison, NJ look for? The top searched job categories for Study Director jobs in Edison, NJ are:
What cities near Edison, NJ are hiring for Study Director jobs? Cities near Edison, NJ with the most Study Director job openings:
Study Director jobs near you
Infographic showing various Study Director job openings in Edison, NJ as of July 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, 1% Temporary, and 2% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $132,893 per year, or $63.9 per hour.
Clinical Study Director

Clinical Study Director

Artech Information System LLC

Bridgewater, NJ

Contractor

Posted 2 days ago

Job description

Company Description

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.

Job Description

This role is key for medical supervision and medical management of clinical trials proposed or to be performed by the Clinical Science & Operations Platform (CSO) of Sanofi R&D. The Clinical Study Director (CSD) is the medical reference in the clinical study and other clinical activities (clinical part of CTD for registration, feasibility, ...) performed by the CSO. The CSD will provide appropriate medical input and support for all these clinical activities. He/she will provide medical training and medical information to study team(s), Clinical Study Units (CSUs) and investigators. He/she will be deeply involved in the feasibility process. He/she will be accountable for medical review and will collaborate and interact with Pharmacovigilance to review safety data. He/she will interact with Medical Advisors in CRUs or Disease Units), a specialization in a medical area would be requested or at least appreciated.

Scope:


All clinical studies related to projects in clinical development (excluding Clinical & Exploratory Pharmacology studies) and medical investigations (e.g. Registry, survey) for projects in development or for marketed drugs.


Key Individual Accountabilities:

Medical reference and medical expertise for operational strategy within the CSO for study registries he/she is allocated to

Medical consultant for projects to be proposed to the CSO

Medical contact for interaction with physicians responsible for the project or the study at the customer level

Support with his/her medical knowledge and background a study or a project from

business negotiation with customers to final product delivery (e.g. study completion or

project report or publication)

Conduct the feasibility for study/project with the feasibility manager and other team members (especially Medical Advisors in CSUs)

Prepare and/or organize and/or participate to Investigator's Meetings, Steering Committees, Data Monitoring Committee meetings (only "open" part of the DMC meetings).

Prepare and/or approve any documents related to the study and requiring a medical expertise (extended synopsis, protocol, medical training material for study monitoring team and for investigators)

Provide medical training to study team, CSUs (Medical Advisors, monitoring) and investigators

Develop interaction with Medical Advisors in CSUs for the best knowledge of the study, compound protocol

Participate to Investigators meetings

Provide medical answers to questions from Health Authorities, IRB/Ethics Committees, investigators, experts

Participate to clinical trial team (and cluster if any) meetings

Accountable for the medical review of data done by the clinical trial team, the case by case review of safety events reported to GPE and coding of events and drugs

Provide appropriate medical input for patient recruitment and retention strategy

Support the CSUs and affiliates to develop network of KOLs and experts and to select National Coordinators or members of Study Committees

Prepare and provide key medical information to investigators and/experts in respect with communication policies (e.g. study results, DMC advice)


Qualifications

Basic Qualifications:

Licensed United States Medical Doctor or an International medical graduate who has certification by the Educational Commission for Foreign Medical Graduates (ECFMG).     

2-3 or more years of Phase 2/3 Clinical Research / Drug Development experience in the pharmaceutical industry. 


Preferred Qualifications:

Knowledge in ICH, GCP and local regulations

Fluent in English (writing and speaking)

Additional Clinical Research and/or Drug Development experience in other therapeutic areas, especially Immunology. 


Additional Information


Sneha Shrivastava

Technical Recruiter (Clinical/Scientific)

 Artech Information Systems LLC

360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 

Office: 973.967.3348 | Fax: 973.998.2599Connect with us on - LinkedIn | Facebook | Twitter



Artech logo

About Artech

Sourced by ZipRecruiter

Artech is a leading IT staffing and consulting company based in Morristown, NJ, US. Since its foundation in 1992, Artech has mastered in complementing human expertise with technology and business acumen to produce world-class staffing solutions. The company caters to diverse industry sectors, including financial services, healthcare, telecommunication, energy and utilities, supply chain, and retail. It provides IT consulting, project management, professional and staff augmentation, and managed staffing services. Artech's mission is to provide exceptional IT staffing services to its clients by comprehending their business needs and then crafting a customized staffing strategy. Its notable achievement includes being recognized as one of the largest IT staffing companies in the U.S, according to Staffing Industry Analysts (SIA).

Industry

Recruiting and staffing services

Company size

10,000+ Employees

Headquarters location

Morristown, NJ, US

Year founded

1992

View All Artech Jobs

Apply