Senior Clinical Research Associate, Sponsor Aligned, Oncology

Key Responsibilities

• Conduct selection, initiation, monitoring, and close-out visits in line with GCP and ICH guidelines.
• Collaborate with sites to develop and track recruitment plans, ensuring project needs are met.
• Provide protocol and study training to sites, maintaining regular communication to manage expectations and address issues.
• Assess site practices for protocol adherence and regulatory compliance, escalating quality issues as needed.
• Oversee regulatory submissions, recruitment, enrollment, CRF completion, and data query resolution. Support start-up phases as required.
• Ensure all site documents are filed in the Trial Master File (TMF) and Investigator’s Site File (ISF) per GCP/ICH and local regulations.
• Generate visit reports, follow-up letters, and other necessary documentation.
• Mentor clinical staff through co-monitoring and training visits.
• Work closely with study team members to support project execution.

Qualifications

• BS degree required; a degree in a scientific discipline or healthcare is preferred.
• 3+ years of on-site oncology monitoring experience strongly preferred. 1.5+ years of oncology monitoring experience can be considered. Phase 1 oncology experience is required.

Skills

• Proficient in GCP and ICH guidelines.
• Strong therapeutic and protocol knowledge in Phase 1 oncology trials.
• Excellent computer skills, including Microsoft Office and mobile devices.
• Effective communication, organizational, and problem-solving abilities.
• Strong time management skills.
• Ability to build and maintain effective working relationships.

Why Join Us?

Be part of a team that’s pushing the boundaries of cancer research. You’ll have the opportunity to work on cutting-edge Phase 1 oncology trials, collaborate with top professionals in the field, and contribute to life-changing advancements in cancer treatment.

IQVIA is a Leading Global Provider of Clinical Research Services

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 at https://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. Learn more.

IQVIA is Committed to Integrity in its Hiring Process

We appreciate your honesty and professionalism. 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.

Where You'll Work

Field-based
You’ll work where the action is — out in the field, directly engaging with our customers, sites or partners. Field-based roles offer the opportunity to build relationships face-to-face, gain real-world insights and make a tangible impact.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Potential Base Pay Range

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).