Job Summary
The Clinical Research Associate – Sponsor Dedicated plays a pivotal role in ensuring the successful execution of clinical trials. This position focuses on overseeing the conduct of clinical studies while working closely with the sponsor to maintain compliance with regulatory standards, protocols, and overall project objectives.
Responsibilities
- Monitor study sites to ensure compliance with clinical trial protocols and regulatory requirements.
- Conduct site visits and evaluations to assess the progress and quality of ongoing clinical trials.
- Collaborate with the sponsor and clinical teams to provide updates on study status and address any issues that arise during the trial.
- Review and verify source documents, case report forms, and site files for accuracy and completeness.
- Ensure that all study activities are executed according to Good Clinical Practice (GCP) guidelines.
Qualifications
- Bachelor’s degree in a life sciences field or a related discipline.
- Prior experience in clinical research as a Clinical Research Associate or similar role.
- In-depth knowledge of clinical trial regulations and GCP guidelines.
- Strong organizational and communication skills to effectively manage multiple tasks.
- Ability to work independently and as part of a team in a fast-paced environment.
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.
