Top 367 Research associate Jobs in Linden Nj

Clinical Research Associate, Full Service
5PY IQVIA RDS Inc. —Parsippany-Troy Hills, NJ
- $47,400 - $169,300 a year
- Full-time
- Microsoft Excel
- Computer literacy
- English
Clinical Research Associate - Part Time
Saint Peter's University Healthcare System —New Brunswick, NJ
- $24.33 - $38.93 an hour
- Part-time
- Hospital
- Mid-level
- Bachelor's degree
- Free parking
- Health insurance
Quick Apply
Clinical Research Associate II
Katalyst Healthcares & Life Sciences —South Plainfield, NJ
- Contract
- Writing skills
- Mid-level
- Communication skills
Quick Apply
Research Associate II
Rutgers University —Newark, NJ
- $65,272 a year
- Full-time
- Medicine
- Mid-level
- 3 years
- Paid holidays
- Dental insurance
Research Clerical Support Assistant
Rutgers University —New Brunswick, NJ
- $20 - $25 an hour
- Part-time
- Psychiatry
- Computer literacy
- Adults
- Paid holidays
- Dental insurance
7d
Clinical Research Associate
Rutgers University —Newark, NJ
- $68,147 a year
- Full-time
- HIPAA
- Mid-level
- Office
- Paid holidays
- Dental insurance
Associate Director, Global Market Research
BioNTech AG —Berkeley Heights, NJ
- $146,300 - $234,100 a year
- Full-time
- Background check
- Office
- 3 years
- Health savings account
- AD&D insurance
Principal Associate, Data Scientist - Mainstreet Acquisitions
Capital One —New York, NY
- Email
- Computer Science
- Research
- AWS
- Health insurance
Clinical Research Assistant, PRN
Care Access —New York, NY
- $19 - $44 an hour
- Part-time
- RN License
- Inventory management
- Pass drug screening
Research Associate
PsychoGenics —Paramus, NJ
- Night shift
- Mid-level
- Surgery
- Bachelor's degree
- Paid parental leave
- Health savings account
Research Technician Interview Day - July 29th, 2026
NYU Langone Health —New York, NY
- $55,649.99 - $55,650.00 a year
- Online Application
- Bachelor of Science
- Research
- Bachelor's degree
- Wellness program
7d
Research Data Associate- Per Diem
NYU Langone Health —New York, NY
- $29.56 an hour
- Part-time
- Microsoft Excel
- Microsoft Outlook
- Computer literacy
- Wellness program
Research Associate
NYU Langone Health —New York, NY
- $47,033.89 - $55,000.00 a year
- Online Application
- Bachelor of Science
- University
- Mentoring
- Wellness program
Research Assistant (Multiple Vacancies)
Rutgers University —Newark, NJ
- $18 - $35 an hour
- Part-time
- Hybrid work
- Computer literacy
- Administrative experience
- University
- Paid holidays
- Dental insurance
Associate Research Scientist (Part-Time)
New York University —New York, NY
- $31 an hour
- Part-time
- Education
- Psychology
- Organizational skills
9d
Clinical Research Associate, IQVIA Biotech
IQVIA —New York, NY
- $71,900 - $169,300 a year
- Full-time
- Bachelor's degree
- Travel
- Experience equivalent to degree accepted
Research Assistant
Barnard College —New York, NY
- $30 an hour
- Part-time
- University
- Entry level
Research Data Associate
NYU Langone Health —New York, NY
- $53,797.97 a year
- Patient monitoring
- Computer literacy
- Writing skills
- Wellness program
Product Research and Development Associate
Truvolt Brands LLC —Jersey City, NJ
- $60,000 a year
- Seasonal
- Office
- Bachelor's degree
- In-person
- Health savings account
- Paid holidays
Assistant Research Associate - Center for Discovery and Innovation- CDI
Hackensack Meridian Health —Nutley, NJ
- From $56,430.40 a year
- Full-time
- Master's degree
- Bachelor's degree
- Organizational skills
- Health insurance
- Dental insurance
11d

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Clinical Research Associate, Full Service

5PY IQVIA RDS Inc. -
Parsippany-Troy Hills, NJ

Apply Now

Job Details

Full-time
$47,400 - $169,300 a year

Qualifications

Computer literacy
Employee relationship building

Full Job Description

Job Overview
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Essential Functions

Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability.
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements.
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
Collaborate and liaise with study team members for project execution support as appropriate.
If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.

Qualifications

Bachelor's Degree Degree in scientific discipline or health care preferred. Req
Equivalent combination of education, training and experience may be accepted in lieu of degree.
Some organizations require completion of CRA training program or prior monitoring experience.
Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).
Good therapeutic and protocol knowledge as provided in company training.
Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
Written and verbal communication skills including good command of English language.
Organizational and problem-solving skills.
Effective time and financial management skills.
Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is proud to be 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, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $47,400.00 - $169,300.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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Refine Your Search

research associate jobs in linden nj

Clinical Research Associate, Full Service

Clinical Research Associate - Part Time

Clinical Research Associate II

Research Associate II

Research Clerical Support Assistant

Clinical Research Associate

Associate Director, Global Market Research

Principal Associate, Data Scientist - Mainstreet Acquisitions

Clinical Research Assistant, PRN

Research Associate

Research Technician Interview Day - July 29th, 2026

Research Data Associate- Per Diem

Research Associate

Research Assistant (Multiple Vacancies)

Associate Research Scientist (Part-Time)

Clinical Research Associate, IQVIA Biotech

Research Assistant

Research Data Associate

Product Research and Development Associate

Assistant Research Associate - Center for Discovery and Innovation- CDI

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