Clinical Research Associate - Sponsor Dedicated

Responsibilities

Conduct all phases of site monitoring activities, including site selection, initiation, routine monitoring, and close-out visits

Evaluate site performance and ensure adherence to study protocols, GCP, ICH guidelines, and applicable regulatory requirements

Partner with investigative sites to develop, implement, and track patient recruitment and retention strategies that support enrollment goals

Deliver protocol-specific training and maintain ongoing communication with site staff to ensure alignment on study expectations and timelines

Identify, document, and escalate quality or compliance concerns while supporting timely resolution of issues

Monitor study progress by tracking regulatory submissions, approvals, enrollment metrics, CRF completion, and data query resolution

Ensure essential study documentation is complete, accurate, and maintained within the Trial Master File (TMF) and Investigator Site File (ISF)

Prepare comprehensive monitoring reports, follow-up letters, and other required study documentation in accordance with company and sponsor standards

Collaborate cross-functionally with project teams to support study execution and achievement of project milestones

May participate in study start-up activities, site budget tracking, financial management, and site payment processes, depending on assignment

Preferred

Bachelor's degree in Life Sciences, Healthcare, Nursing, or a related field preferred

Benefits

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.

Glassdoor

3.9

IQVIA provides analytics, compliance, and management solutions to the life sciences industry.

Durham, North Carolina, USA

https://www.iqvia.com

Public Company

Total Funding

$6.61B

2026-09-09

Post Ipo Debt· $2B

2026-06-04

Post Ipo Debt· $1.11B

2025-06-02

Leadership Team

Karl Guenault

SVP and Chief Information Officer

Chris Colapietro

Vice President, Customer Engagement

Recent News

PR Newswire UK

IQVIA Selects Veeva Clinical Operations Applications

2026-10-16

FierceBiotech

IQVIA, Veeva expand on existing partnership for speedier clinical trials

BioSpace

IQVIA Launches IQVIA Life Science Models to Help Life Sciences Companies Predict Clinical Trial Outcomes

2026-10-08

Company data provided by

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Qualifications

Relevant education and professional experience may be considered in lieu of a degree

Minimum of **2 years of independent on-site monitoring experience** within the pharmaceutical, biotechnology, or CRO industry

Strong understanding of clinical research processes and regulatory requirements, including GCP and ICH guidelines

Knowledge of therapeutic areas and clinical trial protocols gained through industry experience and training

Proficiency with Microsoft Office applications, including Word, Excel, and PowerPoint, as well as mobile and electronic data capture technologies

Excellent verbal and written communication skills with the ability to effectively interact with investigators, site personnel, sponsors, and internal stakeholders

Strong organizational, problem-solving, and time management skills with the ability to manage multiple priorities in a fast-paced environment

Demonstrated ability to work independently while maintaining strong collaborative relationships with colleagues, clients, and study teams

Bachelor's degree in Life Sciences, Healthcare, Nursing, or a related field preferred

Minimum of **2 years of independent on-site monitoring experience** within the pharmaceutical, biotechnology, or CRO industry.

Required skills

Clinical Site Monitoring, Site Management, Clinical Practice (GCP), ICH Guidelines, Clinical Research Processes, Clinical Trial Protocols, Regulatory Requirements, Microsoft Word, Microsoft Excel, Microsoft PowerPoint

Experience

2+ years