United States
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Onsite
Job description
Job Summary
Premier Research is seeking a dedicated Clinical Research Associate (CRA) to enhance our team. This role focuses on organizing and executing clinical monitoring activities at research sites, ensuring compliance with regulatory standards and protocol adherence throughout the study phases.
Responsibilities
- Conduct site monitoring visits throughout various phases of clinical trials.
- Oversee the initiation, routine monitoring, and close-out visits at investigator sites.
- Ensure all activities align with clinical monitoring requirements and sponsor expectations.
- Assist in maintaining the integrity and quality of clinical data.
- Communicate effectively with investigational staff to address study-related queries.
Qualifications
- A degree in a relevant health or life sciences field, or equivalent professional experience.
- Prior experience in clinical research and monitoring is advantageous.
- Ability to work collaboratively in a team-oriented environment.
- Strong organizational and communication skills that facilitate effective interaction with site personnel.
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.
