Company Description

AGA Clinical Trials is a top multicontinent clinical research site based in Miami, Florida. With over 300 trials conducted in different phases and indications, AGA provides access to a diverse patient population and focuses on patient retention. The clinic offers compensation and no-cost study-related medical care to research volunteers, providing advanced medical options not otherwise available.

Role Description

This is a full-time onsite role as a Clinical Research Coordinator at AGA Clinical Trials, located in Hialeah, FL. The Coordinator will be responsible for managing day-to-day tasks related to informed consent, protocols, research, clinical research experience, and clinical trials.

No relocation will be provided.

Candidates in the Miami-Ft. Lauderdale area are preferable.

Qualifications

• Informed Consent and Protocol management skills
• Experience in Clinical Research and as clinical research coordinator, minimal of 2 years.
• Bilingual in English and Spanish is a must.
• Strong attention to detail and organizational skills
• Ability to work collaboratively in a team environment.
• Travel Availability for IM on occasions.
• Ability to work under pressure and tight timelines
• Experience in Blood Draws,samples processing and shipping a must.
• Knowledge of regulatory requirements in clinical research
• Bachelor's degree in a related field, such as Life Sciences or Healthcare
• Certification in Clinical Research is a plus