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Iqvia Medtech Jobs (NOW HIRING)

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 ...

MedTech Site Manager 1

Washington, DC · On-site

$74K - $124K/yr

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 ...

MedTech

Albuquerque, NM · On-site

$25 - $27/hr

IQVIA MedTech CFS takes the approach to helping customers drive healthcare forward in this challenging and fast-paced environment. We help customers accelerate results, improve patient outcomes, and ...

IQVIA MedTech CFS takes the approach to helping customers drive healthcare forward in this challenging and fast-paced environment. We help customers accelerate results, improve patient outcomes, and ...

IQVIA MedTech CFS takes the approach to helping customers drive healthcare forward in this challenging and fast-paced environment. We help customers accelerate results, improve patient outcomes, and ...

IQVIA MedTech CFS takes the approach to helping customers drive healthcare forward in this challenging and fast-paced environment. We help customers accelerate results, improve patient outcomes, and ...

IQVIA MedTech CFS takes the approach to helping customers drive healthcare forward in this challenging and fast-paced environment. We help customers accelerate results, improve patient outcomes, and ...

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Iqvia Medtech information

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$778

$2.1K

$3.2K

How much do iqvia medtech jobs pay per week?

As of Sep 10, 2026, the average weekly pay for iqvia medtech in the United States is $2,120.87, according to ZipRecruiter salary data. Most workers in this role earn between $1,605.77 and $2,596.15 per week, depending on experience, location, and employer.

What is IQVIA MedTech?

IQVIA MedTech is a division of IQVIA that focuses on providing data-driven technology solutions, consulting, and clinical research services to companies in the medical device and diagnostics industry. They help clients navigate regulatory requirements, accelerate product development, and optimize market access strategies. IQVIA MedTech leverages advanced analytics, real-world evidence, and global expertise to support the lifecycle of medical technologies from initial concept through post-market surveillance.

How does working at IQVIA MedTech typically involve collaboration with cross-functional teams?

At IQVIA MedTech, professionals frequently collaborate with cross-functional teams that include data scientists, regulatory experts, clinical researchers, and project managers. This teamwork is essential to deliver comprehensive solutions for medical device development and market access. Employees can expect regular meetings, joint problem-solving, and knowledge sharing, which helps in streamlining project timelines and ensuring compliance with industry standards. Such an environment fosters professional growth and provides exposure to diverse aspects of the medtech industry.

What are the key skills and qualifications needed to thrive as an IQVIA MedTech professional?

To excel at IQVIA MedTech, you typically need a background in life sciences, healthcare, or engineering, along with analytical and project management skills. Familiarity with clinical data management systems, regulatory compliance tools, and proficiency in software like SAS or Medidata Rave are often required. Strong communication, teamwork, and problem-solving abilities help professionals collaborate effectively across global teams and with clients. These competencies are crucial for delivering high-quality solutions in the fast-evolving medical technology sector, ensuring regulatory compliance and client satisfaction.

What is the difference between Iqvia Medtech vs Iqvia Data Analyst?

AspectIqvia MedtechIqvia Data Analyst
Required CredentialsBachelor's in healthcare, engineering, or related field; industry certificationsBachelor's in statistics, data science, or related field; analytical certifications
Work EnvironmentMedical device companies, healthcare technology firms, clinical settingsData-driven departments within healthcare, research organizations, consulting firms
Employer & Industry UsageMedical technology and device manufacturing companiesHealthcare providers, research institutions, analytics firms

While both roles involve working within the healthcare industry, Iqvia Medtech focuses on medical device technology and product development, whereas Iqvia Data Analyst emphasizes data analysis and insights within healthcare data sets. Understanding these differences helps professionals choose the right career path based on their skills and interests.

What is the best Iqvia Medtech job?

The best Iqvia Medtech job depends on individual skills and career goals, but roles such as Medical Device Sales Representative, Clinical Project Manager, or Regulatory Affairs Specialist are highly regarded for their impact and growth opportunities. These positions often require relevant certifications, technical knowledge, and strong communication skills. Advancement typically involves gaining experience and specialized training in medical technology and healthcare regulations.
More about Iqvia Medtech jobs

What states have the most Iqvia Medtech jobs?

States with the most job openings for Iqvia Medtech jobs include:

Infographic showing various Iqvia Medtech job openings in the United States as of September 2026, with employment types broken down into 8% Internship, 87% Full Time, 4% Part Time, and 1% Contract. Highlights an 79% Physical, 2% Hybrid, and 19% Remote job distribution, with an average salary of $110,285 per year, or $53 per hour.

MedTech Site Manager 1

Washington, DC

IQVIA
Health Care and Social Assistance • 10K+ employees

$74K - $124K/yr

Full-time

Posted 27 days ago


IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

63rd of 226 rated it services


Job description

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.Position OverviewThe In-House Clinical Research Associate/MedTech Site Manager 1 will be a critical team member reporting directly to the Director of Clinical Affairs, to support clinical trial operations for the firm's clientele. Responsible for management of investigator site and Clinical Research Associate (CRA) activities for assigned studies. The In-House CRA will execute Clinical Affairs functions in accordance with Good Clinical Practice (GCP) guidelines, Standard Operating Procedures (SOPs), and any other applicable regulatory requirements.Position Responsibilities
  • Review and approve research and study regulatory documents required for the implementation, monitoring, and evaluation of clinical trials.
  • Review clinical protocols to ensure collection of data needed for regulatory submissions
  • Contribute to protocol-specific manuals, plans, and documents as needed.
  • Ensure that monitoring activities (remote and on-site) are completed in accordance with company/client SOPs and Clinical Monitoring Plan.
  • Assist project manager with clinical study planning and management, as required.
  • Develop and maintain positive relationships both internal and external to project, including clients, team members, and site personnel (PIs, Study coordinators, etc.).
  • Assist in the identification and recruitment of potential investigators and study sites, as needed.
  • Ensure Trial Master File is accurate and complete throughout the lifecycle of the project.
  • Assist with site training for assigned clinical trials.
  • Assist with site audits and site quality management activities as needed.
  • Maintain current knowledge of GCP and FDA guidance as it relates to clinical research, as well as current clinical related developments in the assigned therapeutic areas.
Required Qualifications
  • Bachelor's degree (B.A./B.S.) in pharmacy, pharmaceutics or a related scientific discipline
  • 2+ years of clinical trial experience. Monitoring experience preferred.
  • Comprehensive knowledge/ fluency of GCPs and clinical monitoring procedures
  • Understanding of therapeutic area for assigned clinical projects.
  • Experience using Electronic Data Capture (EDC) and clinical trial management systems.
  • Possesses strong written and verbal communication and presentation skills.
  • Strong research, analytical, critical-thinking and problem solving skills
  • PC/Technical skills - MS Office, Excel, Word, PowerPoint (Endnote experience is a plus)

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 $74,500.00 - $124,100.00. 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.

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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