Top 10 Clinical research coordinator associate Jobs in New York Ny

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
Clinical Research Associate
Rutgers University —Newark, NJ
- $68,147 a year
- Full-time
- HIPAA
- Mid-level
- Office
- Paid holidays
- Dental insurance
Clinical Research Associate (CRA) - Cardiovascular/Vaccine/Infectious Disease- Remote
Merck —Rahway, NJ
- $96,200 - $151,400 a year
- Full-time
- Remote
- English
- Mid-level
- Microsoft Office
- Paid holidays
- Health insurance
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
Senior Clinical Research Associate
ICON Plc —New York, NY
- $110,520 - $138,150 a year
- Full-time
- Remote
- RN License
- English
- US work authorization
- Disability insurance
- Health insurance
11d
Clinical Research Associate II
Katalyst Healthcares & Life Sciences —South Plainfield, NJ
- Contract
- Writing skills
- Mid-level
- Communication skills
Quick Apply
Senior Clinical Research Associate - Cardiovascular Medical Device
T45 Labs —New York, NY
- $113,000 - $153,000 a year
- Email
- Remote
- Nursing
- 7 years
- Bachelor's degree
Quick Apply
4d
Associate Director, Quality Assurance (Clinical Research Preferred)
IQVIA —Wayne, NJ
- $88,600 - $246,600 a year
- Full-time
- Remote
- Nursing
- Bachelor's degree
- Mentoring
- Work from home
Associate Director, Clinical Research
NS Pharma —Paramus, NJ
- $175,000 - $205,000 a year
- Hybrid work
- 8 years
- Bachelor's degree
- Contracts
- Paid parental leave
- Health savings account
Associate Director, Clinical Research
NS Pharma Inc —Paramus, NJ
- $175,000 - $205,000 a year
- 8 years
- Bachelor's degree
- Contracts
- Paid parental leave
- Health savings account
Quick Apply

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Clinical Research Associate, IQVIA Biotech

IQVIA -
New York, NY

Apply Now

Job Details

Full-time
$71,900 - $169,300 a year

Qualifications

Regulatory compliance
ICH guidelines
Clinical quality assurance standards
Oncology

Full Job Description

New York, United States of America | Full time | Field-based | R1520467

IQVIA Biotech is now hiring for CRA 2 with a minimum of 1 year of on-site monitoring and will also consider CRA 1 candidates with a minimum of 6 months on-site monitoring experience. Must have experience monitoring in oncology solid tumor.

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.

Job Overview
We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in ensuring the successful execution of clinical trials. In this position, you will be responsible for monitoring and managing clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations. Your work will directly contribute to the integrity and quality of clinical research data.

Key Responsibilities

Conduct all types of site visits—selection, initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines.
Collaborate with site staff to implement and track subject recruitment strategies that align with project timelines and enrollment goals.
Deliver protocol and study-specific training to site personnel and maintain consistent communication to manage expectations and resolve issues.
Assess site performance and adherence to the protocol, escalating quality concerns as needed to ensure compliance and data integrity.
Monitor study progress by tracking regulatory submissions, subject enrollment, case report form (CRF) completion, and resolution of data queries.
Ensure that essential documents are collected and maintained in both the Trial Master File (TMF) and the Investigator Site File (ISF) in accordance with regulatory standards.
Document site management activities, visit outcomes, and follow-up actions through detailed reports and correspondence.
Work closely with cross-functional project teams to support study execution and ensure alignment with project goals.
Depending on the project, you may also support site-level recruitment planning and financial management, including invoice collection and budget tracking.

Qualifications

Bachelor’s degree in life sciences or health-related field (or equivalent experience).
Requires at least 1 year of on-site monitoring experience.
Strong understanding of GCP, ICH guidelines, and regulatory requirements.
Ability to travel as required by the project.

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 $71,900.00 - $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

clinical research coordinator associate jobs in new york ny

Clinical Research Associate, IQVIA Biotech

Clinical Research Associate

Clinical Research Associate (CRA) - Cardiovascular/Vaccine/Infectious Disease- Remote

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

Senior Clinical Research Associate

Clinical Research Associate II

Senior Clinical Research Associate - Cardiovascular Medical Device

Associate Director, Quality Assurance (Clinical Research Preferred)

Associate Director, Clinical Research

Associate Director, Clinical Research

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