Top 107 Iqvia Jobs in New York, Ny

Contract Virtual Clinical Coordinator
IQVIA —New York, NY
- $33,000 - $82,600 a year
- Full-time
- Remote
- Patient monitoring
- Mid-level
- 3 years
- Work from home
Freelance Independent Rater
IQVIA —New York, NY
- $62,700 - $156,700 a year
- Part-time
- Remote
- Psychiatry
- Clinic experience
- Mid-level
- Work from home
- Flexible schedule
2d
CRA 1, IQVIA Biotech
IQVIA —New York, NY
- $71,900 - $145,300 a year
- Full-time
- Bachelor's degree
- Travel
- Communication skills
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
Linguistic Validation & eCOA Project Manager
IQVIA —New York, NY
- $59,800 - $149,500 a year
- Full-time
- Remote
- Customer service
- Mid-level
- 3 years
- Work from home
15h
Senior Product Manager, IQVIA Digital
IQVIA —New York, NY
- $100,200 - $278,900 a year
- Full-time
- Remote
- HIPAA
- 8 years
- Presentation skills
- Work from home
Flex Nurse Educator - New York, NY
IQVIA —New York, NY
- $80,000 - $85,000 a year
- Weekends as needed
- Remote
- Spanish
- Nursing
- Up to 50% travel
1d
Scientific Advisor, Medical Communications
IQVIA —New York, NY
- $99,300 - $248,300 a year
- Full-time
- Remote
- 3 years
- Doctor of Philosophy
- Travel
- Work from home
Client Transition Specialist
IQVIA —Parsippany-Troy Hills, NJ
- $73,400 - $183,600 a year
- Full-time
- Mid-level
- Office
- Bachelor's degree
MedTech - Registered Nurse Clinical Educator
IQVIA —New York, NY
- $35 - $38 an hour
- Part-time
- Nursing
- RN License
- Mid-level
10d
Health Information Technology Specialist East
IQVIA —New York, NY
- $125,000 - $135,000 a year
- Full-time
- System design
- Mid-level
- Master's degree
Clinical Program Manager
IQVIA —Parsippany-Troy Hills, NJ
- $93,100 - $285,500 a year
- Full-time
- Remote
- Bachelor's degree
- Conflict management
- Senior level
- Work from home
Project Manager, eCOA Implementation
IQVIA —Wayne, NJ
- $88,100 - $220,200 a year
- Full-time
- Remote
- Mid-level
- Bachelor's degree
- Mentoring
- Work from home
8d
Clinical Trial Psych Rater - US Spanish Speaking
IQVIA —New York, NY
- $62,700 - $156,700 a year
- Part-time
- Remote
- Nursing
- Medicine
- Psychiatry
- Work from home
15h
Project Lead - RUA92307
IQVIA —New York, NY
- $200,000 - $225,000 a year
- Full-time
- Nursing
- Driver's License
- Travel
13d
Medical Director, Medical & Scientific Communications
IQVIA —New York, NY
- $134,300 - $374,300 a year
- Full-time
- Remote
- Medicine
- Doctor of Philosophy
- Travel
- Work from home
CRA 2/Senior CRA 1
IQVIA —New York, NY
- $90,200 - $175,100 a year
- Full-time
- Bachelor's degree
- Experience equivalent to degree accepted
- 1 year
CRA 2/Senior CRA
IQVIA —New York, NY
- $90,200 - $175,100 a year
- Full-time
- Mid-level
- Bachelor's degree
- Experience equivalent to degree accepted
Consultant, Arc Bio Communications
IQVIA —New York, NY
- $68,300 - $170,000 a year
- Full-time
- Mid-level
- Office
- 4 years
Site Activation Manager
IQVIA —Wayne, NJ
- $86,500 - $216,000 a year
- Full-time
- Remote
- Bachelor's degree
- Team management
- Mentoring
- Work from home

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Contract Virtual Clinical Coordinator

IQVIA -
New York, NY

Apply Now

Job Details

Full-time
$33,000 - $82,600 a year

Benefits

Work from home

Qualifications

Bachelor's degree

Full Job Description

New York, United States of America | Full time | Home-based | R1557999

MCRA is part of IQVIA MedTech. As a trusted CRO and advisory partner, IQVIA MedTech and MCRA deliver integrated lifecycle solutions for the medical device and diagnostics industry. Together, we support innovation from concept to commercialization, offering expertise in regulatory strategy, clinical trial design and execution, market access, and post-market optimization. Our teams combine deep therapeutic knowledge with advanced data and technology to help clients make smarter decisions and thrive in the market. Join our team to help shape the future of MedTech.

Overview

The Virtual Clinical Coordinator (temp/fixed term) plays a critical role in supporting the execution of clinical research studies by coordinating and performing remote clinical activities in compliance with study protocols, Standard Operating Procedures (SOPs), and Good Clinical Practice (GCP). This role is responsible for performing a variety of clinical procedures to collect, record, report, and interpret patient data for individuals enrolled in or seeking enrollment in clinical studies.

Responsibilities and Duties

Adhere to SOPs and Manual of Procedures when conducting all study-related activities to ensure compliance and consistency. This includes maintaining a working knowledge of study-specific software applications and equipment.
Collaborate with the research team and study sites to identify, recruit, and virtually enroll eligible patients for clinical trials.
Collect, maintain, and securely store all relevant data associated with clinical research trials in accordance with regulatory and organizational standards.
Educate potential participants about clinical research trials, including study requirements, and manage the informed consent process through virtual interactions.
Assist with participant study compliance by providing guidance and reminders to ensure adherence to protocol requirements.
Conduct follow-up activities for clinical trials while maintaining adherence to Good Clinical Practice (GCP) guidelines.
Ensure patient safety by monitoring participants, reporting adverse events promptly, and ensuring compliance with IRB-approved protocols.
Support the research participant call center as assigned, handling inquiries and providing assistance.
Maintain professionalism in all interactions with research participants to foster trust and engagement.
Assist with study equipment management and reporting, ensuring proper tracking, functionality, and documentation.
Communicate effectively with MCRA clinical affairs staff and clients, providing updates and support under the guidance of senior MCRA staff as needed.
Perform additional duties and projects as assigned to support the success of clinical research operations.

Required Knowledge, Skills, and Experience

Education: Bachelor’s degree required (preferably in a life sciences or healthcare-related field)
Experience: Minimum of three years of experience as a Clinical Coordinator or in a comparable clinical research role
Strong attention to detail
Excellent verbal and written communication skills

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 $33,000.00 - $82,600.00. 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

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

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

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Overview

Responsibilities and Duties

Adhere to SOPs and Manual of Procedures when conducting all study-related activities to ensure compliance and consistency. This includes maintaining a working knowledge of study-specific software applications and equipment.

Collaborate with the research team and study sites to identify, recruit, and virtually enroll eligible patients for clinical trials.

Collect, maintain, and securely store all relevant data associated with clinical research trials in accordance with regulatory and organizational standards.

Educate potential participants about clinical research trials, including study requirements, and manage the informed consent process through virtual interactions.

Assist with participant study compliance by providing guidance and reminders to ensure adherence to protocol requirements.

Conduct follow-up activities for clinical trials while maintaining adherence to Good Clinical Practice (GCP) guidelines.

Ensure patient safety by monitoring participants, reporting adverse events promptly, and ensuring compliance with IRB-approved protocols.

Support the research participant call center as assigned, handling inquiries and providing assistance.

Maintain professionalism in all interactions with research participants to foster trust and engagement.

Assist with study equipment management and reporting, ensuring proper tracking, functionality, and documentation.

Communicate effectively with MCRA clinical affairs staff and clients, providing updates and support under the guidance of senior MCRA staff as needed.

Perform additional duties and projects as assigned to support the success of clinical research operations.

Required Knowledge, Skills, and Experience

Education: Bachelor’s degree required (preferably in a life sciences or healthcare-related field)

Experience: Minimum of three years of experience as a Clinical Coordinator or in a comparable clinical research role

Strong attention to detail

Excellent verbal and written communication skills

Where you'll work

Home-based

Culture