Job Summary
IQVIA is looking for a dedicated (Senior) Clinical Research Associate to join our team in Durham, North Carolina. This position requires an onsite presence to oversee clinical trials by performing site monitoring visits and ensuring adherence to study protocols.
Responsibilities
- Conduct site monitoring visits to verify compliance with clinical trial protocols.
- Establish and nurture solid relationships with investigative sites to enhance performance and recruitment efforts.
- Maintain oversight and monitoring of the protocol adherence throughout the trials.
- Collaborate with various stakeholders to facilitate the smooth progression of clinical studies.
Qualifications
- Proven experience in clinical research monitoring, especially in a similar role.
- Strong understanding of regulatory requirements and clinical trial processes.
- Excellent communication and relationship-building skills.
- Ability to work collaboratively in a team-oriented 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.
