Job description
Job Summary
The Clinical Research Coordinator I – Bilingual (Spanish) plays a vital role in the management and oversight of clinical trials. This position requires a proficient understanding of regulatory compliance and the capability to communicate effectively with diverse stakeholders, ensuring that clinical studies run smoothly and meet all research objectives.
Responsibilities
- Assist in the coordination and implementation of clinical trial protocols.
- Recruit, screen, and enroll study participants while ensuring informed consent is obtained.
- Maintain accurate and organized documentation of clinical trial activities.
- Monitor study progress and ensure adherence to regulatory guidelines and Good Clinical Practice (GCP).
- Communicate effectively with both English and Spanish-speaking participants throughout the study process.
- Collaborate with investigators and sponsor representatives to facilitate study operations.
Qualifications
- Bachelor’s degree in a relevant field or equivalent experience.
- Fluency in Spanish and English, both spoken and written.
- Strong organizational skills with the ability to manage multiple tasks simultaneously.
- Effective communication and interpersonal skills to interact with diverse populations.
- Understanding of clinical trial regulations and compliance standards.
Location
City, State Zip
Work Arrangement
On-site
