Top 164 Clinical Research Associate Jobs in Raritan, 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
6d
Clinical Research Associate
Theradex Oncology —Princeton, NJ
- $75,000 - $90,000 a year
- Full-time
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Disability insurance
- Health insurance
21h
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
2d
Clinical Research Associate II
Katalyst Healthcares & Life Sciences —South Plainfield, NJ
- Contract
- Writing skills
- Mid-level
- Communication skills
Quick Apply
Senior Clinical Research Associate-Contractor
SystImmune —Princeton, NJ
- Full-time
- Remote
- Nursing
- Up to 50% travel
- 5 years
Manager, Clinical Adjudication Operations
Daiichi Sankyo, Inc. —Basking Ridge, NJ
- $127,280 - $190,920 a year
- 3 years
- Master's degree
- Bachelor's degree
Director, Risk Based Quality Management (RBQM)
Daiichi Sankyo, Inc. —Basking Ridge, NJ
- $201,840 - $302,760 a year
- Hybrid work
- Master's degree
- Bachelor's degree
- Travel
Sr. Clinical Scientist/Associate Director, Clinical Science
Celldex Therapeutics, Inc. —Hampton, NJ
- $133,579 - $199,501 a year
- Full-time
- Microsoft Word
- 5 years
- Bachelor of Science
- Health savings account
- Paid holidays
Associate Director - External Data Acquisition Lead (EDAL)
Genmab —Plainsboro, NJ
- $157,360 - $236,040 a year
- Online Application
- Master's degree
- Bachelor's degree
- Mentoring
- Commuter assistance
- Paid parental leave
Director, Clinical Operations - AAV
Rocket Pharmaceuticals —Cranbury, NJ
- $196,000 - $294,000 a year
- Full-time
- Microsoft Outlook
- 8 years
- Bachelor's degree
- Paid holidays
- Health insurance
8d
Senior Manager, Inspection Readiness
Genmab —Princeton, NJ
- $64,000 - $195,840 a year
- Online Application
- 8 years
- Mentoring
- Senior level
- Commuter assistance
- Paid parental leave
13d
Senior Manager, Clinical Programming
Genmab —Princeton, NJ
- $131,040 - $196,560 a year
- Online Application
- Computer science
- 6 years
- Computer Science
- Commuter assistance
- Paid parental leave
Senior Programming Manager
Genmab —Plainsboro, NJ
- $128,080 - $192,120 a year
- Online Application
- Computer Science
- Master's degree
- 8 years
- Commuter assistance
- Paid parental leave
Clinical Trial Manager
Genmab —Princeton, NJ
- $119,120 - $178,680 a year
- Online Application
- 5 years
- Master's degree
- Bachelor's degree
- Commuter assistance
- Paid parental leave
Director, Strategic Clinical Vendor Oversight and Relationship Lead (CRO)
Genmab —Princeton, NJ
- $193,280 - $289,920 a year
- Online Application
- 8 years
- Bachelor's degree
- Training & development
- Commuter assistance
- Paid parental leave
Clinical Research Associate- West Coast
Zydus Therapeutics Inc. —Pennington, NJ
- $100,000 - $110,000 a year
- Remote
- Microsoft Excel
- Microsoft Outlook
- Computer literacy
Quick Apply
Contract, Clinical Trial Associate
PTC Therapeutics, Inc. —Warren, NJ
- $35 - $47 an hour
- Full-time
- Microsoft Word
- Microsoft Excel
- Mid-level
Quick Apply
9d
Clinical Trial Associate
Novo Nordisk —Plainsboro, NJ
- $70,000 - $123,000 a year
- Weekends as needed
- Customer service
- English
- Mid-level
- Disability insurance
- Health insurance
1d
Associate Research Scientist: Immunoassays
Thermo Fisher Scientific —Lawrenceville, NJ
- $90,000 - $110,000 a year
- Online Application
- 6 years
- Mid-level
- Bachelor's degree
- Commuter assistance
- Paid parental leave
Contract - Clinical Trial Associate, Clinical Operations
Shionogi Inc. —Florham Park, NJ
- $40 - $60 an hour
- Email
- Hybrid work
- Microsoft Excel
- Customer service
- Bachelor of Science

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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
6 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

Clinical Research Associate jobs in Raritan, NJ

Clinical Research Associate, Full Service

Clinical Research Associate

Clinical Research Associate - Part Time

Clinical Research Associate II

Senior Clinical Research Associate-Contractor

Manager, Clinical Adjudication Operations

Director, Risk Based Quality Management (RBQM)

Sr. Clinical Scientist/Associate Director, Clinical Science

Associate Director - External Data Acquisition Lead (EDAL)

Director, Clinical Operations - AAV

Senior Manager, Inspection Readiness

Senior Manager, Clinical Programming

Senior Programming Manager

Clinical Trial Manager

Director, Strategic Clinical Vendor Oversight and Relationship Lead (CRO)

Clinical Research Associate- West Coast

Contract, Clinical Trial Associate

Clinical Trial Associate

Associate Research Scientist: Immunoassays

Contract - Clinical Trial Associate, Clinical Operations

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