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 may be offered, dependent on the position offered.
• Bonuses may be offered, dependent on the position 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
• FierceBiotech
• Aligning drug discovery around patient benefit from the outset: Connecting human insights to better decisions
• 2026-10-20
• PR Newswire UK
• IQVIA Selects Veeva Clinical Operations Applications
• 2026-10-16
• IQVIA, Veeva expand on existing partnership for speedier clinical trials
• 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

• Clinical Practice (GCP), Clinical Trial Documentation, International Conference on Harmonization (ICH) Guidelines, Microsoft Office, On-Site Clinical Monitoring, Oncology Clinical Research

Preferred skills

• 2 years preferred

Experience

• 1+ years