Job Summary
The role of the Clinical Research Associate is central to the seamless operation of study sites, particularly in the field of oncology. This position, located in Parsippany, New Jersey, requires an onsite presence to oversee critical activities and ensure compliance with all regulatory standards.
Responsibilities
- Oversee and support the operational aspects of clinical trials.
- Maintain and manage essential documentation within the Trial Master File (TMF) as well as the Investigator’s Site File (ISF) to meet regulatory obligations.
- Work collaboratively with study sites to enhance efficiency and compliance.
Qualifications
- Experience in clinical research, particularly in an oncology environment is preferred.
- Strong understanding of regulatory requirements and guidelines related to clinical trials.
- Excellent organizational skills and attention to detail.
- Ability to effectively communicate and collaborate with diverse teams.
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.
