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Clinical Research Associate Sponsor Dedicated Jobs

IQVIA

$71K - $189K/yr

... sponsor requirements. Essential Functions Perform site monitoring visits (selection, initiation ... Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. i.e ...

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How much do clinical research associate sponsor dedicated jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for clinical research associate sponsor dedicated in the United States is $41.13, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $52.64 per hour, depending on experience, location, and employer.

What is a clinical research associate sponsor dedicated?

A Clinical Research Associate (CRA) Sponsor Dedicated is a professional who monitors clinical trials on behalf of a pharmaceutical or biotechnology company (the sponsor), rather than working for a contract research organization (CRO). Their primary responsibility is to ensure that clinical studies are conducted in compliance with protocols, regulations, and good clinical practice (GCP) guidelines. They act as a liaison between the sponsor and research sites, overseeing data accuracy, patient safety, and regulatory documentation. Being sponsor dedicated means they work exclusively for one sponsor, allowing for deeper familiarity with that company’s processes and studies.

How does a clinical research associate sponsor dedicated typically interact with clinical sites and sponsor teams during a study?

As a Clinical Research Associate (Sponsor Dedicated), you will serve as a crucial liaison between the sponsor and clinical sites. Your responsibilities include monitoring site compliance, ensuring data integrity, and providing training or support to site staff. You will regularly communicate with both the sponsor’s project team and site personnel to address issues, resolve queries, and facilitate smooth trial operations. This role often involves travel to clinical sites, frequent status updates with sponsor representatives, and participation in team meetings to discuss study progress and challenges.

What are the key skills and qualifications needed to thrive as a clinical research associate sponsor dedicated, and why are they important?

To thrive as a Clinical Research Associate Sponsor Dedicated, a solid understanding of clinical trial processes, Good Clinical Practice (GCP), and a relevant life sciences degree are essential. Familiarity with electronic data capture (EDC) systems, regulatory compliance software, and often a GCP certification are typically required. Strong organizational skills, attention to detail, and effective communication help ensure smooth collaboration between sponsors, sites, and regulatory bodies. These skills are vital for maintaining data integrity, regulatory compliance, and the successful execution of clinical trials.

What is the difference between Clinical Research Associate Sponsor Dedicated vs Clinical Research Associate?

AspectClinical Research Associate Sponsor DedicatedClinical Research Associate
CredentialsTypically requires a degree in life sciences, nursing, or related field; certifications like CCRA or RAC are commonSame as Sponsor Dedicated, often with similar certifications and educational background
Work EnvironmentWorks closely with sponsor teams, often in dedicated clinical trial units or officesWorks across multiple sites, monitoring clinical trials in various locations
Employer & Industry UsageEmployed by sponsors or CROs with a focus on specific sponsor trialsEmployed by CROs, pharmaceutical companies, or biotech firms, overseeing multiple trials

Both roles require similar qualifications and certifications, but the Clinical Research Associate Sponsor Dedicated primarily works within a sponsor's dedicated team, focusing on specific trials, while the Clinical Research Associate generally monitors multiple sites across various trials.

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Clinical Research Associate Sponsor Dedicated jobs near you
Infographic showing various Clinical Research Associate Sponsor Dedicated job openings in the United States as of August 2026, with employment types broken down into 2% As Needed, 74% Full Time, 15% Part Time, and 9% Contract. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution, with an average salary of $85,542 per year, or $41.1 per hour.

Clinical Research Associate, Sponsor Dedicated

IQVIA

Santa Fe, NM

$71K - $189K/yr

Full-time

Re-posted 24 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

To be eligible for this position, you must reside in the same country where the job is located.
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.
Essential Functions
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.
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 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.
i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Good therapeutic and protocol knowledge as provided in company training.
Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
Written and verbal communication skills including good command of English language.
Organizational and problem-solving skills.
Effective time and financial management skills.
Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

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 $71,900.00 - $189,000.00. 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

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