Top 346 Research associate Jobs in Whippany Nj

Clinical Research Associate, Full Service
IQVIA —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
Rutgers University —Newark, NJ
- $68,147 a year
- Full-time
- HIPAA
- Mid-level
- Office
- Paid holidays
- Dental insurance
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
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
14d
Research Associate
Columbia University —New York, NY
- $33.90 an hour
- Part-time
- Microsoft Excel
- Computer literacy
- Mid-level
Clinical Research Associate II / Sr. CRA (MDD Experience), Northeast US
Rho Inc —New York, NY
- $100,000 - $145,000 a year
- Full-time
- Remote
- Nursing
- Computer literacy
- Bachelor of Science
- Health savings account
- Paid holidays
Quick Apply
13h
Associate Research Scientist (Part-Time)
New York University —New York, NY
- $26 an hour
- Part-time
- University
- Experience working with children
- Bachelor's degree
Research Associate Position in Stem Cell Biology and Neuroscience
Rutgers University —Piscataway, NJ
- From $85,588 a year
- Full-time
- Mid-level
- University
- Doctor of Philosophy
- Paid holidays
- Dental insurance
Summer Research Associate (Campus)
Société Générale —New York, NY
- $105,000 a year
- Multiple hires
- Hybrid work
- Office
- Analysis skills
- Internship
- Wellness program
- Paid holidays
14d
Clinical Research Associate II
Katalyst Healthcares & Life Sciences —South Plainfield, NJ
- Contract
- Writing skills
- Mid-level
- Communication skills
Quick Apply
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
Research Associate
Surgery Center of Oradell —Oradell, NJ
- Full-time
- Entry level
Business Research Assistant (Part-Time, Remote/Hybrid)
Edible Arrangements —Teaneck, NJ
- $18 - $22 an hour
- Part-time
- Hybrid work
- In-person
- Marketing
- Entry level
Quick Apply
Assistant Research Scientist (Part-Time)
New York University —New York, NY
- $18 an hour
- Part-time
- Remote
- Organizational skills
- Entry level
Research Associate II
Rutgers University —Newark, NJ
- $65,272 a year
- Full-time
- Mid-level
- 3 years
- Master's degree
- Paid holidays
- Dental insurance
Temporary Research Assistant
Rutgers University —New Brunswick, NJ
- $15.92 - $150.00 a day
- Part-time
- Microsoft Word
- Microsoft Excel
- Computer literacy
- Paid holidays
- Dental insurance
Research Data Associate
NYU Langone Health —New York, NY
- $53,797.97 a year
- Patient monitoring
- Computer literacy
- Writing skills
- Wellness program
Research Associate
The Stevenson Group —Fort Lee, NJ
- Microsoft Outlook
- Mid-level
- Bachelor's degree
Research Assistant
Columbia University —New York, NY
- $34.74 an hour
- Part-time
- Microsoft Outlook
- SQL
- Bachelor's degree

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Clinical Research Associate, Full Service

IQVIA -
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

Parsippany, United States of America | Full time | Field-based | R1497311

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.

Where you'll work

Field-based

You’ll work where the action is — out in the field, directly engaging with our customers, sites or partners. Field-based roles offer the opportunity to build relationships face-to-face, gain real-world insights and make a tangible impact.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Apply Now

Refine Your Search

research associate jobs in whippany nj

Clinical Research Associate, Full Service

Clinical Research Associate - Part Time

Clinical Research Associate

Research Data Associate- Per Diem

Assistant Research Associate - Center for Discovery and Innovation- CDI

Research Associate

Clinical Research Associate II / Sr. CRA (MDD Experience), Northeast US

Associate Research Scientist (Part-Time)

Research Associate Position in Stem Cell Biology and Neuroscience

Summer Research Associate (Campus)

Clinical Research Associate II

Research Assistant (Multiple Vacancies)

Research Associate

Business Research Assistant (Part-Time, Remote/Hybrid)

Assistant Research Scientist (Part-Time)

Research Associate II

Temporary Research Assistant

Research Data Associate

Research Associate

Research Assistant

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