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Study Director Jobs in Raritan, NJ (NOW HIRING)

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 ...

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 ...

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, Bioanalytical

Cranbury, NJ

$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 ...

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 ...

WuXi AppTec

Senior Scientist I

Cranbury, NJ · On-site

$93K - $127K/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 ...

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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 ...

Icon plc

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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Showing results 21-40

All JobsStudy JobsStudy Director JobsStudy Director Jobs in Raritan, NJ

Study Director information

See Raritan, NJ salary details

$46.1K

$131.5K

$238.1K

How much do study director jobs pay per year?

As of Sep 7, 2026, the average yearly pay for study director in Raritan, NJ is $131,453.00, according to ZipRecruiter salary data. Most workers in this role earn between $59,400.00 and $193,000.00 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 job categories do people searching Study Director jobs in Raritan, NJ look for?

The top searched job categories for Study Director jobs in Raritan, NJ are:

What cities near Raritan, NJ are hiring for Study Director jobs?

Cities near Raritan, NJ with the most Study Director job openings:

Study Director jobs near you
Infographic showing various Study Director job openings in Raritan, NJ as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 13% Part Time, 1% Temporary, and 3% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $131,453 per year, or $63.2 per hour.

Scientist III

WuXi AppTec

Cranbury, NJ

$90K - $110K/yr

Full-time

Re-posted 26 days ago

Job description

The Scientist III would lead the development of new ADME studies and technologies and implementing process improvements. Perform method validation, report writing, complex trouble-shooting and problem-solving in the field of drug discovery and development.


  • 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 discovery and development studies.
  • Supervises personnel. Ensures optimum personnel performance through leading by example, motivation, and performance recognition.
  • Writes comprehensive reports and presents clear and concise oral reports of processes and accomplishments.
  • Maintains research notebooks in a well-organized manner.  All necessary documentation is recorded.
  • Trains junior level scientists.
  • Reviews other scientists’ calculations and records.
  • Follows company’s safety policies, practices and procedures in order to maintain a safe work environment, practices good housekeeping, and maintains safe workplace without supervision.
  • Learns, enhances, and shares technical knowledge of pharmaceutical areas, DMPK, ADME, In Life, Metabolism, and Bioanalysis.
  • Participates in writing and review of Standard Operating Procedures (SOPs) and suggests practical changes.
  • Other duties as assigned.

Experience / Education: 

  • PhD., Master’s or Bachelor's degree in Biology, Chemistry, or other related Physical science degree.
  • PhD with 0-3 years related experience. Master’s degree with 8+ years related experience, Bachelor’s degree with 10+ years related experience or equivalent combination of education and/or work experience. 

 Knowledge / Skills / Abilities:

  • An expert in advanced experimental methods, concepts and techniques relevant to ADME field.
  • Demonstrates independent thought and scientific/technical creativity.
  • Continues to increase awareness and understanding of relevant science and is conversant with relevant scientific literature.
  • Collaboratively researches and proposes methodologies for projects
  • Acts independently to research and propose methodologies and implement them
  • Effective oral and written communication and interpersonal skills
  • Good time management skill to perform multiple projects within deadlines.
  • Ability to work in a team environment.
  • Follow and adhere to nonGLP guidelines/SOPs consistent with WuXi AppTec requirement.

The anticipated base salary range for this opening is $90,000 to $110,000.

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