United States
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Onsite
Job description
Job Summary
Premier Research is seeking a Clinical Research Associate I to become a part of our Clinical Monitoring, Site Management, and SSU team. In this role, you will play a vital part in supporting biotech and medtech organizations by ensuring compliance and quality during clinical trials.
Responsibilities
- Support the execution of clinical studies under guidance and supervision.
- Contribute to the management of site performance and monitor adherence to protocols.
- Assist in data collection and analysis to ensure accurate reporting.
- Coordinate with clinical teams to facilitate effective communication between sites and stakeholders.
- Maintain compliance with regulatory requirements throughout the clinical trial process.
Qualifications
- Must hold a license as a health-care professional, such as a registered nurse, or possess equivalent relevant experience.
- Ability to work effectively with clinical teams and manage multiple tasks.
- Strong attention to detail and organizational skills.
- Excellent communication skills, both verbal and written.
Premier Research 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.
