United States
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Onsite
Job description
Job Summary
Premier Research is seeking a Clinical Research Associate II to join our team in the United States. This position involves performing various tasks related to clinical monitoring, ensuring that clinical trials are conducted in accordance with applicable regulations and protocols.
Responsibilities
- Conduct monitoring visits at investigator sites to oversee the progress of clinical trials.
- Perform initiation, interim, and close-out visits as necessary to ensure compliance with study protocols.
- Collaborate with site staff and provide guidance on protocol requirements and study procedures.
- Document findings and maintain accurate records of monitoring activities.
- Ensure that study data is collected accurately and in accordance with regulatory standards.
Qualifications
- A degree in a relevant field, such as nursing (e.g., registered nurse), or equivalent professional experience is required.
- Prior experience in clinical research monitoring is preferred.
- Strong understanding of Good Clinical Practice (GCP) and regulatory requirements.
- Excellent communication and interpersonal skills for effective collaboration with clinical sites.
- Detail-oriented with strong organizational skills to manage multiple responsibilities.
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.
