Tampa, Florida, 33602
Apply now
Onsite
Job description
Job Summary
The Clinical Research Associate – Sponsor Dedicated role involves overseeing clinical trials and ensuring compliance with regulatory requirements. This position is essential for managing site operations, fostering relationships with investigators, and enhancing collaboration among site personnel to facilitate successful study outcomes.
Responsibilities
- Monitor the progress of clinical trials and ensure adherence to protocols.
- Develop and maintain effective relationships with study sites and investigators.
- Ensure compliance with regulatory standards and internal policies.
- Assist in the training and on-boarding of site staff.
- Conduct site visits to assess trial progress and data integrity.
Qualifications
- Bachelor’s degree in Life Sciences, Healthcare, Nursing, or a related field is preferred.
- Experience as a Clinical Research Associate (CRA II/Sr. CRA) in multiple therapeutic areas.
- Strong interpersonal and communication skills to build relationships with site personnel.
- Familiarity with clinical trial processes and regulatory requirements.
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.
