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
ObjectiveHealth 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.
