Job Summary
The Clinical Research Associate (CRA) plays a pivotal role in the management and oversight of clinical trials. This position ensures compliance with regulatory requirements, company standards, and ethical guidelines throughout the research process. The CRA will coordinate between various stakeholders, including clinical sites and sponsors, to facilitate successful trial execution and maintain data integrity.
Responsibilities
- Monitor the progress of clinical trials ensuring adherence to protocol and regulatory compliance.
- Conduct site selection, initiation, monitoring, and closeout visits.
- Ensure proper documentation of trial-related activities and data integrity.
- Communicate regularly with clinical sites to address issues and provide guidance.
- Collaborate with project teams to ensure timely reporting and resolution of site-related issues.
- Assist in training site personnel on study protocols and procedures.
Qualifications
- Bachelor’s degree in life sciences or a related field.
- Previous experience in clinical research or a similar role preferred.
- Strong understanding of clinical trial regulations (e.g., GCP, FDA regulations).
- Excellent communication and interpersonal skills.
- Detail-oriented with strong organizational abilities.
- Proficiency in using clinical trial management software and electronic data capture systems.
BD (Becton, Dickinson and Company) 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.
