Sr. CRA 1, IQVIA

Responsibilities

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

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

Preferred

Bachelor's Degree in scientific discipline or health care preferred

Benefits

Incentive plans, bonuses, and/or other forms of compensation may be offered.

A range of health and welfare and/or other benefits may be offered.

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

Qualifications

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

Bachelor's Degree in scientific discipline or health care preferred

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

Required skills

Clinical Site Monitoring, Clinical Research Regulatory Requirements, Clinical Practice (GCP), International Conference on Harmonization (ICH) Guidelines, Therapeutic and Clinical Study Protocol Knowledge

Experience

2+ years