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Study Director Jobs in New York (NOW HIRING)

Azenta

Study Director

South Plainfield, NJ · On-site

$79K - $99K/yr

Study Director I Location: South Plainfield, NJ Shift: M-F 9am-5pm At GENEWIZ, from Azenta Life Sciences, new ideas, new technologies and new ways of thinking are driving our future. Our customer ...

New

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.

NS Pharma Inc

Director, Clinical Research

Paramus, NJ · On-site

Direct and manage the performance of study vendors (e.g., CROs and central labs). * Provide direction and guidance with the Clinical Lead to achieve project objectives. * Manage and resolve project ...

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Study Director information

See New York salary details

$49.2K

$140.4K

$254.4K

How much do study director jobs pay per year?

As of Aug 29, 2026, the average yearly pay for study director in New York is $140,438.00, according to ZipRecruiter salary data. Most workers in this role earn between $63,500.00 and $206,200.00 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.

More about Study Director jobs

What are the most commonly searched types of Study jobs in New York?

The most popular types of Study jobs in New York are:

What are popular job titles related to Study Director jobs in New York?

For Study Director jobs in New York, the most frequently searched job titles are:

What job categories do people searching Study Director jobs in New York look for?

The top searched job categories for Study Director jobs in New York are:

What cities in New York are hiring for Study Director jobs?

Cities in New York with the most Study Director job openings:

Study Director jobs near you
Infographic showing various Study Director job openings in New York as of August 2026, with employment types broken down into 2% As Needed, 81% Full Time, 14% Part Time, 1% Temporary, and 2% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $140,438 per year, or $67.5 per hour.

Study Director

Azenta

South Plainfield, NJ • On-site

$79K - $99K/yr

Full-time

Posted 2 days ago

New

Azenta Life Sciences rating

7.5

Company rating: 7.5 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

63rd of 120 rated laboratories

Job description

Azenta Inc.At Azenta, new ideas, new technologies and new ways of thinking are driving our future. Our customer focused culture encourages employees to embrace innovation and challenge the status quo with novel thinking and collaborative work relationships.
All we accomplish is grounded in our core values of Customer Focus, Achievement, Accountability, Teamwork, Employee Value and IntegrityJob TitleStudy DirectorJob Description

Position Title: Study Director I

Location: South Plainfield, NJ

Shift: M-F 9am-5pm

At GENEWIZ, from Azenta Life Sciences, new ideas, new technologies and new ways of thinking are driving our future. Our customer-focused culture encourages employees to embrace innovation and challenge the status quo with novel thinking and collaborative work relationships.

GENEWIZ is a global leader in multiomics and synthetic solution services with headquarters in South Plainfield, NJ and offices and operations worldwide. We empower our customers' research by providing high-quality, precision-based solutions from discovery through clinical development, enabling scientists to make breakthroughs faster and more efficiently. Key services include Next Generation and Sanger sequencing, gene synthesis, gene-to-discovery solutions including antibody production, viral packaging and mRNA synthesis. Together with our customers, we can be the partner of choice for life science communities worldwide, driving advancements that foster innovation across the globe.

How You'll Make an Impact

The position is responsible for overseeing a range of molecular biology techniques, including PCR, sequencing, cloning, and related analyses to support project objectives. The role involves independently managing multiple project types, analyzing data, troubleshooting experiments, reviewing records, preparing reports, and strict adherence to the Azenta Quality System. This position oversees assigned GLP studies and ensures accurate documentation and communication through internal systems and customer interactions. The ideal candidate demonstrates strong technical proficiency, attention to detail, and effective communication skills in a team environment.

What You'll Do

  • Provide operations team with instructions for PCR and sequencing, Plasmid DNA Preparation, cDNA/gDNA Verification, DNA Cloning and related molecular biology projects where applicable
    • Related tasks to include but are not limited to: PCR amplification, post-reaction preparations, sequencing data analysis, mutation analysis, DNA/RNA extractions, cDNA generation, DNA transformation, and restriction digest analysis.
  • Oversee GLP Studies in the Study Director role including protocol generation, batch record review, data analysis, and reporting.
  • Contribute and/or independently execute project design, data analysis, troubleshooting and reporting.
  • Knowledge of using CLIMS for sample submission/data retrieval for sequencing orders as well as project data delivery.
  • Communicate with customers by phone and e-mail in a friendly and professional manner to assist with simple troubleshooting efforts.
  • Additional tasks as assigned by supervisor.

What You Will Bring

  • Meet Study Director requirements as outlined by the managers of RS and QA.
  • Knowledge of Molecular Biology techniques.
  • In-depth knowledge of the regulations for Good Laboratory Practice (GLP): 21CFRpart58; 40CFRpart160.
  • 5+ years of previous lab or analysis experience is preferred.
  • Bachelor's degree in Life Sciences is required.
  • Master's degree in Life Sciences is preferred.

Physical Demands/Work Environment

  • Must be onsite at least 4 days per week to support in-person team collaboration.

record review, data analysis, and reporting.

EOE M/F/Disabled/VET

If any applicant is unable to complete an application or respond to a job opening because of a disability, please email at Recruiting@azenta.com for assistance.

Azenta is an Equal Opportunity Employer. This company considers candidates regardless of race, color, age, religion, gender, sexual orientation, gender identity, national origin, disability or veteran status.

United States Base Compensation: $79,000.00 - $99,000.00

The posted pay range for this position is an estimate based on current market data and internal pay structure. Final compensation may vary above or below this range depending on factors such as experience, education (including licensure and certifications), qualifications, performance, and geographic location, among other relevant business or organizational needs.

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