Top 3 Iqvia Jobs in Columbia, Sc

CRA 2/Senior CRA 1
IQVIA —Columbia, SC
- $90,200 - $175,100 a year
- Full-time
- Bachelor's degree
- Experience equivalent to degree accepted
- 1 year
MedTech Part Time Clinical Consultant – East Bay, San Francisco, CA
IQVIA —United States
- $85 an hour
- Part-time
- RN License
- Mid-level
- 3 years
MedTech Part Time Clinical Consultant – San Francisco, CA
IQVIA —United States
- $85 an hour
- Part-time
- RN License
- Mid-level
- 3 years

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MedTech Part Time Clinical Consultant – East Bay, San Francisco, CA
IQVIA —United States
Must provide a minimum of (2) days of live support within the field (case support, patient rounding, providing education), with a total of (5) days of…
$85 an hour

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CRA 1, IQVIA Biotech
IQVIA —Columbus, OH
During these visits, you will review essential documents, assess protocol adherence, oversee data entry and query resolution, and ensure maintenance of both the…
$71,900 - $145,300 a year
MedTech Part Time Clinical Consultant – East Bay, San Francisco, CA
IQVIA —United States
Must provide a minimum of (2) days of live support within the field (case support, patient rounding, providing education), with a total of (5) days of…
$85 an hour

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CRA 2/Senior CRA 1

IQVIA -
Columbia, SC

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Job Details

Full-time
$90,200 - $175,100 a year

Qualifications

Regulatory compliance
ICH guidelines
Clinical quality assurance standards

Full Job Description

Columbia, United States of America | Full time | Field-based | R1547445

Join a Team That’s Advancing Clinical Research

We’re looking for a passionate and driven Clinical Research Associate (CRA) to join our team and play a key role in delivering high-quality clinical trials. In this role, you’ll partner with investigative sites and cross-functional teams to ensure studies are executed with excellence, compliance, and patient focus.

What You’ll Do

Lead and execute site monitoring visits (selection, initiation, routine, and close-out) in accordance with GCP/ICH guidelines
Build strong relationships with investigative sites to drive performance, recruitment, and engagement
Ensure protocol compliance, data integrity, and high-quality study execution
Proactively identify risks, resolve issues, and escalate when needed
Track and manage study progress, including regulatory approvals, enrollment, and data quality
Maintain accurate documentation and contribute to inspection readiness
Collaborate with cross-functional teams to ensure successful study delivery

What You Bring

Bachelor’s degree in life sciences, healthcare, or related field (or equivalent experience)
1.5+ years of on-site monitoring experience
Solid understanding of GCP, ICH, and regulatory requirements
Strong communication, problem-solving, and organizational skills
Ability to manage multiple priorities in a fast-paced environment

Why Join Us

Make a direct impact on advancing clinical research and improving patient outcomes
Work alongside experienced, collaborative teams
Opportunities for growth and career development
Dynamic, fast-paced environment where your contributions matter

If you’re ready to take the next step in your CRA career and be part of meaningful, impactful work, we’d love to hear from you.

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 $90,200.00 - $175,100.00. 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.

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iqvia jobs in columbia, sc

CRA 2/Senior CRA 1

MedTech Part Time Clinical Consultant – East Bay, San Francisco, CA

MedTech Part Time Clinical Consultant – San Francisco, CA