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Study Director Jobs in Edison, NJ (NOW HIRING)

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Clinical Study Specialist

Warren, NJ · Hybrid

$62K - $77K/yr

Clinical Study Specialist - Hybrid role: Warren, NJ, Armonk NY or Cambridge MA ICON is a global ... Communication with sites as directed and maintains site contact information * Contributes to line ...

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Clinical Study Specialist

New York, NY · Hybrid

$62K - $77K/yr

Clinical Study Specialist (Hybrid - Warren, NJ, Armonk, NY or Cambridge MA)) ICON is a global ... Communication with sites as directed and maintains site contact information * Contributes to line ...

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Clinical Study Specialist

Warren, NJ · Hybrid

$62K - $77K/yr

Clinical Study Specialist (Hybrid - Warren, NJ, Armonk, NY or Cambridge MA)) ICON is a global ... Communication with sites as directed and maintains site contact information * Contributes to line ...

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Clinical Study Specialist

Warren, NJ · Hybrid

$62K - $77K/yr

Clinical Study Specialist (Hybrid office/home based in Warren NJ, Armonk NY or Cambridge MA) ICON ... Communication with sites as directed and maintains site contact information * Contributes to line ...

ICON

Clinical Study Specialist

Warren, NJ · On-site

$62K - $77K/yr

Clinical Study Specialist (Hybrid office/home based in Warren NJ, Armonk NY or Cambridge MA) ICON ... Communication with sites as directed and maintains site contact information * Contributes to line ...

Eurofins

Sample Extraction Manager

New Brunswick, NJ · On-site

The Sample Extraction Manager serves as a primary technical and operational contact for clients, Study Directors, and laboratory personnel regarding extraction and preparation requirements. This ...

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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 Sep 7, 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 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 Edison, NJ?

The most popular types of Study jobs in Edison, NJ are:

What are popular job titles related to Study Director jobs in Edison, NJ?

For Study Director jobs in Edison, NJ, the most frequently searched job titles 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 August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 13% Part Time, 1% Temporary, and 2% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $132,893 per year, or $63.9 per hour.

Clinical Study Specialist

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Warren, NJ • Hybrid

$62K - $77K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted yesterday

Job description

Clinical Study Specialist - Hybrid role: Warren, NJ, Armonk NY or Cambridge MA

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


What you will be doing

  • Organizes and delivers analyzable reports and metrics to the clinical study lead

  • Schedules and coordinates meetings, prepares agendas, presentation materials and minutes for clinical study team meetings and other study related meetings

  • Collates data for assessments such as feasibility and site selection and reviews site usability database

  • Contributes to review of study documents such as informed consent forms, case report forms and facilitates study document reviews per company standard operating procedures

  • Compiles study manuals including but not limited to: study reference binders and manuals and maintains versioning of study reference materials (e.g., regulatory, pharmacy, and laboratory binders

  • Collates materials for training and investigator meetings

  • Tracks site activation, enrolment and monitoring visits to projected plans, and escalate any issues or delays with site activation or deviations from monitoring plan

  • Monitors and updates investigator/site status for the trial, and supports with clinical trial registry postings

  • Performs scheduled reconciliations of study Trial Master File (TMF) with clinical study lead guidance

  • Ensures scheduled reports are received (i.e. 1572 reportable changes, financial disclosure form)

  • Manages and maintains team SharePoint and/or shared drive sites, as needed

  • Communication with sites as directed and maintains site contact information

  • Contributes to line listings review for Blind Data Review Meeting (BDRM)

  • May manage or contribute to oversight of Third Party Vendors (TPV)

  • Tracks and monitors close out activities - study close-out documents (1572s, Investigational Product reconciliation, Financial Disclosures, etc.) and CRA close-out visits

  • Participates in Standard Operating Procedures (SOPs) revisions or departmental initiatives

  • Proactively recommends process improvement initiatives for the department

Your profile

  • Must have a Bachelor's Degree

  • Must have a minimum of 2 years industry related work experience

  • Experience supporting global trials (NA, LAM, EU, APAC, India)

  • Experience working in TMF, CTMS, Sharepoint,

  • Excels in written and verbal communications

  • Self-starter, can work independently with minimal oversight, solution-oriented

  • ICF review experience

  • General competency: powerpoint/excel skills, meeting minutes

  • Vendor management/oversight experience a plus

  • Must be open to hybrid office/home based in Warren NJ, Armonk NY or Cambridge MA


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a requesthere.

Salary Range

$62,376.00-$77,970.00

Are you a current ICON Employee? Please click here to apply

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