Top 363 Research Associate Jobs in Rahway, 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
10d
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
5d
Clinical Research Associate II
Katalyst Healthcares & Life Sciences —South Plainfield, NJ
- Contract
- Writing skills
- Mid-level
- Communication skills
Quick Apply
Associate Scientist-Analytical R&D
Ascendia Pharmaceuticals —North Brunswick, NJ
- $40,000 - $70,000 a year
- Temporary
- Bachelor of Science
- Laboratory experience
- Mid-level
- Health savings account
- Health insurance
Quick Apply
Clinical Research Assistant, PRN
Care Access —New York, NY
- $19 - $44 an hour
- Part-time
- RN License
- Inventory management
- Pass drug screening
Clinical Research Assistant, PRN (Phlebotomist, LVN or Registered Nurse)
Care Access —New York, NY
- $19 - $44 an hour
- Part-time
- RN License
- Inventory management
- Pass drug screening
Research Support Associate
Rutgers University —Newark, NJ
- $32,219 - $95,000 a year
- Part-time
- Microsoft Excel
- Mid-level
- Office
- Paid holidays
- Dental insurance
Clinical Research Associate (CRA) - Oncology (Remote)
Merck —Rahway, NJ
- $96,200 - $151,400 a year
- Full-time
- Remote
- English
- Mid-level
- Microsoft Office
- Paid holidays
- Health insurance
3d
Clinical Research Associate (CRA) - Immunology-Remote
Merck —Rahway, NJ
- $96,200 - $151,400 a year
- Full-time
- Remote
- English
- Mid-level
- Microsoft Office
- Paid holidays
- Health insurance
3d
Clinical Research Associate
Rutgers University —Newark, NJ
- $68,147 a year
- Full-time
- HIPAA
- Mid-level
- Office
- Paid holidays
- Dental insurance
6d
Research Associate, Cardiac Surgery Research
Newark Beth Israel Medical Center —Newark, NJ
- $25 - $30 an hour
- Full-time
- Microsoft Excel
- Surgery
- Mid-level
- Disability insurance
- Health insurance
Temporary Research Assistant
Rutgers University —Newark, NJ
- $25 an hour
- Part-time
- Mid-level
- Master's degree
- University
- Paid holidays
- Dental insurance
6d
Temporary Research Assistant (Sexual/Reproductive Health)
Rutgers University —Newark, NJ
- $22 - $25 an hour
- Part-time
- University
- Bachelor's degree
- Editing
- Paid holidays
- Dental insurance
Temporary Research Assistant (multiple openings)
Rutgers University —Piscataway, NJ
- $18 - $25 an hour
- Part-time
- University
- Communication skills
- Editing
- Paid holidays
- Dental insurance
Research Associate
Columbia University —New York, NY
- $33.90 an hour
- Part-time
- Microsoft Excel
- Computer literacy
- Mid-level
Student Assistant (Research)
Rutgers University —Newark, NJ
- $15.49 an hour
- Part-time
- University
- Communication skills
- Public Health
- Paid holidays
- Dental insurance
6d
Research Associate (Tischfield Lab)
Rutgers University —Piscataway, NJ
- From $85,588 a year
- Full-time
- Mid-level
- University
- Doctor of Philosophy
- Paid holidays
- Dental insurance
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 II
Rutgers University —Piscataway, NJ
- $65,272 a year
- Full-time
- English
- Mid-level
- 3 years
- Paid holidays
- Dental insurance
13d
Research Study Assistant
Rutgers University —New Brunswick, NJ
- $30.35 an hour
- Full-time
- Mid-level
- Office
- University
- Paid holidays
- Dental insurance

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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
10 days ago

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 Rahway, NJ

Clinical Research Associate, Full Service

Clinical Research Associate - Part Time

Clinical Research Associate II

Associate Scientist-Analytical R&D

Clinical Research Assistant, PRN

Clinical Research Assistant, PRN (Phlebotomist, LVN or Registered Nurse)

Research Support Associate

Clinical Research Associate (CRA) - Oncology (Remote)

Clinical Research Associate (CRA) - Immunology-Remote

Clinical Research Associate

Research Associate, Cardiac Surgery Research

Temporary Research Assistant

Temporary Research Assistant (Sexual/Reproductive Health)

Temporary Research Assistant (multiple openings)

Research Associate

Student Assistant (Research)

Research Associate (Tischfield Lab)

Research Assistant (Multiple Vacancies)

Research Associate II

Research Study Assistant

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