Job Summary
The Clinical Research Associate, Sponsor Dedicated, plays a critical role in overseeing and managing clinical trials on behalf of sponsors. This position requires a detail-oriented individual who can ensure that the clinical studies adhere to regulatory requirements and that data integrity is maintained throughout the research process. The Associate will act as a primary contact between the sponsor and clinical sites, ensuring effective communication and smooth operational flow of the trials.
Responsibilities
- Monitor clinical trial sites to ensure adherence to Good Clinical Practice (GCP) and regulatory guidelines.
- Review and assess site performance, project timelines, and budgets to guarantee successful trial execution.
- Collaborate with site personnel to provide training and support during the study to maximize compliance and efficiency.
- Conduct regular site visits to evaluate recruitment progress, patient safety, and data accuracy.
- Facilitate issue resolution between sites and sponsor while fostering a positive relationship with clinical teams.
Qualifications
- A bachelor’s degree in life sciences, nursing, or a related field is typically required.
- Prior experience as a Clinical Research Associate or in a similar position is highly preferred.
- Strong knowledge of ICH-GCP guidelines and relevant regulatory requirements.
- Excellent communication and organizational skills to manage multiple projects effectively.
- Proficiency in clinical trial management software and Microsoft Office Suite.
IQVIA provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
