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Iqvia Jobs in Raleigh, NC (NOW HIRING)

IQVIA

Sr. Clinical Research Associate, IQVIA

Durham, NC

$87K - $169K/yr

IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology, cardiovascular, renal, metabolic, CNS, Obesity (GLP-1), diabetes, GI, MASH/NASH, dermatology, or respiratory:

IQVIA, Inc.

CRA 2, Oncology, IQVIA

Durham, NC · On-site

$87K - $145K/yr

IQVIA is seeking a CRA 2 with a minimum of 1.5 years of on-site oncology monitoring experience: Essential Functions Perform site monitoring visits (selection, initiation, monitoring and close-out ...

IQVIA

Clinical Research Associate 2, IQVIA

Durham, NC · On-site

$71K - $189K/yr

IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in IM/GI, MASH/NASH, dermatology and/or asthma/respiratory clinical trials. Women's Health experience is a plus! Job ...

IQVIA

Sr. Clinical Research Associate, IQVIA

Durham, NC · On-site

$87K - $169K/yr

IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology, cardiovascular, renal, metabolic, CNS, Obesity (GLP-1), diabetes, GI, MASH/NASH, dermatology, or respiratory:

IQVIA

Clinical Research Associate 2, IQVIA

Durham, NC · On-site

$71K - $189K/yr

IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in CNS, GLP-1/Obesity/Diabetes (Type II) and/or Cardiovascular clinical trials. Phase 1 experience is a plus! Job ...

IQVIA

Clinical Research Associate 2, IQVIA

Durham, NC

$71K - $189K/yr

IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in IM/GI, MASH/NASH, dermatology and/or asthma/respiratory clinical trials. Women's Health experience is a plus! Job ...

IQVIA

Clinical Research Associate 2, IQVIA

Durham, NC

$71K - $189K/yr

IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in CNS, GLP-1/Obesity/Diabetes (Type II) and/or Cardiovascular clinical trials. Phase 1 experience is a plus! Job ...

IQVIA Argentina

CRA 2, Oncology, IQVIA

Durham, NC · On-site

$87.20 - $145.30/hr

Job Overview Durham, United States of America | Full time | Field-based | R1537618 IQVIA is seeking a CRA 2 with a minimum of 1.5 years of on-site oncology monitoring experience: This role focuses on ...

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Iqvia information

What is IQVIA?

IQVIA is a global leader in providing advanced analytics, technology solutions, and contract research services to the life sciences industry. The company helps pharmaceutical, biotechnology, and medical device firms with clinical research, real-world data insights, and consulting to improve healthcare outcomes. IQVIA combines deep industry expertise with big data and artificial intelligence to support drug development, commercialization, and patient engagement. Their services are widely used for designing clinical trials, managing regulatory submissions, and optimizing market access strategies.

What types of projects do employees typically work on at IQVIA, and how does collaboration occur across different teams?

At IQVIA, employees often work on projects related to healthcare data analytics, clinical research, and pharmaceutical consulting. Teams are interdisciplinary, so you may collaborate closely with data scientists, project managers, and client-facing consultants to deliver insights or solutions to life sciences clients. The environment encourages frequent communication through meetings, shared platforms, and cross-functional task forces, ensuring project goals are met efficiently. This collaborative structure provides opportunities to learn from diverse expertise and contribute to impactful healthcare advancements.

What are the key skills and qualifications needed to thrive as an IQVIA Clinical Research Associate, and why are they important?

To thrive as a Clinical Research Associate at IQVIA, you need a solid background in life sciences, clinical trial processes, and a relevant degree such as nursing, pharmacy, or biology. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) certification, and clinical trial management software is typically required. Excellent organizational skills, attention to detail, and effective communication are crucial soft skills for managing multiple studies and collaborating with research sites. These competencies ensure studies are conducted ethically, data integrity is maintained, and regulatory compliance is achieved.

What is the difference between Iqvia vs Clinical Data Analyst?

AspectIqviaClinical Data Analyst
Required CredentialsBachelor's degree in life sciences, healthcare, or related field; experience with data managementBachelor's degree in health informatics, statistics, or related field; proficiency in data analysis tools
Work EnvironmentPharmaceutical and healthcare research settings, often corporate or contract-basedClinical research sites, hospitals, or research organizations
Employer & Industry UsageMajor provider of clinical trial data, analytics, and technology solutionsAnalyzing clinical trial data to support research and regulatory submissions

While both roles involve working with clinical data, Iqvia focuses on providing data solutions and analytics services to the healthcare industry, often in a corporate setting. Clinical Data Analysts primarily analyze clinical trial data within research environments. The roles share similar credentials but differ in scope and work environment.

What are popular job titles related to Iqvia jobs in Raleigh, NC?

For Iqvia jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Iqvia jobs in Raleigh, NC look for?

The top searched job categories for Iqvia jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Iqvia jobs?

Cities near Raleigh, NC with the most Iqvia job openings:

Iqvia jobs near you
Infographic showing various Iqvia job openings in Raleigh, NC as of August 2026, with employment types broken down into 77% Full Time, 21% Part Time, and 2% Contract. Highlights an 77% Physical, 2% Hybrid, and 21% Remote job distribution.

Sr. Clinical Research Associate, IQVIA

IQVIA

Durham, NC

$87K - $169K/yr

Full-time

Re-posted 5 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 224 rated it services

Job description

IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology, cardiovascular, renal, metabolic, CNS, Obesity (GLP-1), diabetes, GI, MASH/NASH, dermatology, or respiratory:

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.

Key Responsibilities:

Perform site monitoring visits (selection, initiation, monitoring, and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.

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) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP 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. Responsibilities Essential Functions 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 in scientific discipline or health care preferred.

Requires at least 2 years of year of on-site monitoring experience.

Equivalent combination of education, training and experience may be accepted in lieu of degree.

Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.

Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

Good therapeutic and protocol knowledge as provided in company training.

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 athttps://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 $87,200.00 - $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.

What IQVIA employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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