Senior Clinical Research Associate, Sponsor Aligned, Oncology

Sr. CRA, Sponsor Aligned, Oncology page is loaded## Sr. CRA, Sponsor Aligned, Oncologylocations:
Overland Park, KS, United States of America:
Carlsbad, CA, United States of America time type:
Full time posted on:
Posted Todayjob requisition :
R1541483

Job Overview:  Join our dynamic team as a Clinical Research Associate! You’ll play a pivotal role in monitoring and managing clinical trial sites to ensure compliance with study protocols, regulations, and sponsor requirements. Be at the forefront of groundbreaking cancer research and make a real impact on patients’ lives.

Key Responsibilities  Site Monitoring Visits:
Conduct selection, initiation, monitoring, and close-out visits in line with GCP and ICH guidelines.  Subject Recruitment:
Collaborate with sites to develop and track recruitment plans, ensuring project needs are met.  Training & Communication:
Provide protocol and study training to sites, maintaining regular communication to manage expectations and address issues.  Quality Assurance:
Assess site practices for protocol adherence and regulatory compliance, escalating quality issues as needed.  Study Progress Management:
Oversee regulatory submissions, recruitment, enrollment, CRF completion, and data query resolution. Support start-up phases as required.  Documentation:
Ensure all site documents are filed in the Trial Master File (TMF) and Investigator’s Site File (ISF) per GCP/ICH and local regulations.  Reporting:
Generate visit reports, follow-up letters, and other necessary documentation.  Mentorship:
Mentor clinical staff through co-monitoring and training visits.

Collaboration:

Work closely with study team members to support project execution.

Qualifications

Education:

BS degree required; a degree in a scientific discipline or healthcare is preferred.

Experience:

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  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.

If you’re passionate about making a difference and have the expertise we’re looking for, we’d love to hear from you!

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. 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 atIQVIA 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.

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of…