Job Summary
The position of Clinical Research Associate in Early Clinical Development at IQVIA offers an exciting opportunity for professionals based in Boston, Massachusetts. This role focuses on managing and overseeing clinical trials to ensure compliance with regulatory requirements while maintaining documentation standards.
Responsibilities
- Manage and monitor the progress of clinical trials to ensure adherence to protocols.
- Ensure all necessary documentation is accurately maintained in both the Trial Master File (TMF) and Investigator Site File (ISF).
- Work collaboratively with clinical teams to support and facilitate effective trial execution.
- Communicate with stakeholders to provide updates on study progress and resolve any issues that arise.
- Assist in ensuring trials meet all regulatory and ethical standards.
Qualifications
- Previous experience in clinical research or a related field is preferred.
- Strong understanding of regulatory guidelines and compliance requirements.
- Excellent organizational and communication skills.
- Ability to work effectively in a team environment and adapt to various challenges.
- Proficiency in relevant software and data management tools.
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.
