Job Summary
IQVIA is in search of a Clinical Research Associate II who possesses comprehensive independent on-site monitoring experience to become a vital part of our team located in Durham, North Carolina. This role involves ensuring that clinical trials are conducted in compliance with regulatory standards while fostering effective partnerships with investigative sites.
Responsibilities
- Conduct thorough monitoring of clinical study sites to ensure adherence to protocols and regulatory requirements.
- Establish and nurture strong working relationships with investigative sites.
- Provide updates and guidance related to protocol, processes, and specific study details to site staff.
Qualifications
- Experience in independent on-site monitoring in clinical research is essential.
- Familiarity with regulatory requirements and adherence to clinical protocols.
- Strong communication and relationship-building skills are crucial.
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.
