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Study Director Jobs in Edison, NJ (NOW HIRING)

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 ...

Icon plc

Clinical Study Specialist

Warren, NJ · Hybrid

$62K - $77K/yr

Clinical Study Specialist (Hybrid) ICON is a global healthcare intelligence and clinical research ... 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 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 Aug 8, 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 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 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.

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.
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, 84% Full Time, 13% Part Time, 1% Temporary, and 1% 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.

Senior Scientist I, Bioanalytical

WuXi AppTec

Cranbury, NJ • On-site

$93K - $127K/yr

Other

Posted 25 days ago

Job description

The Senior Scientist I is responsible for the day-to-day coordination and supervision of the team operation to ensure the successful implementation of the DMPK Non-GLP Bioanalytical method development, method qualification, sample analysis, report writing, and metrics in order to deliver outstanding customer satisfaction in the field of drug discovery and development.

  • Designs, plans and carries out the more complex research studies including method development for the analytes and its metabolites in various matrices. Provides multiple approaches during the planning step.
  • Trains, coaches, or mentors others on technical, personal development or business issues.
  • Works on extremely complex problems in which analysis of situations or data requires an evaluation of intangible variables. Exercises independent judgment in developing methods, techniques and evaluation criteria for obtaining results.
  • 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 exacting research studies.
  • Supervises personnel. Ensures optimum personnel performance through leading by example, motivation, and performance recognition.
  • Conducting quick PK sample analysis in variety of biological matrices, including but not limited to stock solution preparation, sample extraction, small or large molecule sample analysis, and report writing.
  • Reviews other scientists’ calculations, records, and reports. Writes comprehensive reports, recommending application of finings, and presents clear and concise oral reports of processes and accomplishments.
  • Complies with all safety rules, practice good housekeeping, and maintain 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 suggest practical changes.
  • Promotes company’s safety policies, practices and procedures in order to maintain a safe work environment.
  • Other duties as assigned.
  • PhD or Master’s degree in chemistry, Biology, or related Physical science degree. PhD with 3+ years related work experience.  Or Master’s degree with 10+ years related work experience. 

Knowledge / Skills / Abilities:

  • An expert in the use of advanced experimental methods, concepts and techniques relevant to scientific discipline and specific area, such small or large molecule bioanalytical, including LC-MS, ELISA/MSD, PCR, flow cytometry, western blotting, etc,
  • Demonstrated experience in the independent development of LBA and/or LC-MS bioanalytical methods.
  • Emerging skills in novel experimental methods, concepts and techniques
  • Demonstrates independent thought and scientific creativity
  • Demonstrates technical success and proficiency in projects
  • Utilizes expert knowledge of scientific principles and concepts
  • Collaboratively researches and proposes methodologies for projects
  • Acts independently to research and propose new research projects and methodologies and implement them
  • Good time management skills in order to perform multiple projects within deadlines
  • Expected to initiate external publications and presentations
  • Effective oral and written communication and interpersonal skills
  • Good time management skill in order to perform of multiple projects within deadlines
  • Ability to work in a team environment
  • Follow and adhere to nonGLP guidelines/SOPs consistent with WuXi AppTec requirement

 

Physical Requirements: 

  • Must be able to work in an office environment with minimal noise conditions.
  • Must be able to work in Lab setting with exposure to biohazards / chemicals
  • Must be able to wear appropriate PPE
  • Must be able to work in environment with variable noise levels
  • Ability to stand /Sit/walk for long periods of time
  • Ability to Lift 15 lbs routinely
  • Ability to crouch, bend, twist, and reach
  • Ability to push/pull 15 lbs routinely
  • Clarity of Vision
  • Ability to identify and distinguish colors
  • Must be able to perform activities with repetitive motions
  • Ability to work in variable temperatures high to freezing

 

An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability

This job description does not state or imply that the above are the only duties and responsibilities assigned to this position.  Employees holding this position will be required to perform any other job-related duties as requested by Management.

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