What are the responsibilities and job description for the Clinical Research Coordinator position at AGA Clinical Trials?
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 a clinical research coordinator, a minimum of 2 years.
- Bilingual in English and Spanish is mandatory.
- 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 phlebotomy, sample 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 ( MA, Nursing, FMG)