Clinical Research Associate, Sponsor Dedicated, Oncology

Responsibilities

Conduct selection, initiation, monitoring, and close-out visits, ensuring compliance with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

Collaborate with sites to develop and track recruitment plans, ensuring project needs are met

Provide protocol training and maintain regular communication with sites to manage expectations and address issues

Evaluate site practices for protocol adherence and escalate quality issues as needed

Track regulatory submissions, recruitment, enrollment, and data management to ensure smooth study progress

Maintain essential documents in the Trial Master File (TMF) and Investigator’s Site File (ISF) as per regulatory requirements

Mentor clinical staff through co-monitoring and training visits

Work closely with study team members to support project execution

Manage site finances and retrieve invoices as per local requirements

Preferred

2 years preferred

Benefits

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

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

Qualifications

• Education: BS Degree in a scientific discipline or healthcare preferred
• Experience: Minimum 1 year of on-site monitoring experience in oncology
• Knowledge: Strong understanding of GCP and ICH guidelines, with expertise in oncology protocols
• Skills: Proficiency in Microsoft Office, excellent communication skills, and strong organizational and problem-solving abilities
• Attributes: Effective time and financial management, and the ability to build strong working relationships

2 years preferred

• Experience: Minimum 1 year of on-site monitoring experience in oncology;

Required skills

Oncology Clinical Trial Monitoring, Clinical Practice (GCP), International Council for Harmonisation (ICH) Guidelines, Oncology Protocols, Microsoft Office

Preferred skills

2 years preferred

Experience

1+ years