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 and Site Management team. In this position, you will collaborate closely with clinical sites to support the execution of clinical trials, ensuring compliance with regulatory standards and protocols. The role is integral to the advancement of our research initiatives.
Responsibilities
- Monitor clinical trial sites for adherence to protocols and regulations.
- Develop and maintain strong relationships with study sites and personnel.
- Assist in the training of site staff on study protocols.
- Ensure accurate and timely data collection and reporting.
- Conduct patient-facing activities as required during studies.
Qualifications
- A licensed healthcare professional, such as a registered nurse, or equivalent experience is mandatory.
- Strong understanding of clinical trial processes and regulatory requirements.
- Excellent communication and interpersonal skills to foster collaboration with site staff.
- Ability to manage multiple tasks and prioritize effectively in a dynamic environment.
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.
