Alcanza Clinical Research is seeking a Clinical Research Coordinator to join their team in Largo, FL. The role involves ensuring the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations, and SOPs.
About the Role
As a Clinical Research Coordinator, you will collaborate with the clinical research site team to execute assigned studies. Your responsibilities will include screening patients for study enrollment, obtaining patient consents, conducting follow-up visits, documenting in source clinic charts, entering data in EDC, obtaining vital signs and ECGs, performing basic lab procedures, maintaining logs, scheduling subjects for visits, and ensuring compliance with study protocols.
About You
Required:
A Medical Assistant diploma, LPN/LVN, EMT credential OR Associate’s degree AND a minimum of 1 year of clinical research or clinical experience.
Proficiency with computer applications such as Microsoft applications, email, electronic health records, and the ability to type proficiently (40+ wpm).
Strong organizational skills and attention to detail.
Well-developed written and verbal communication skills.
Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.
Preferred:
Proficiency with performing basic clinical procedures such as blood pressure, vitals, EKGs, phlebotomy, etc.
Bi-lingual (English / Spanish) proficiency.
Benefits
Medical, dental, vision, life insurance, short and long-term disability insurance.
Health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match.
Coverage starting on the first day of the month following date of hire for full-time employees.
Alcanza Clinical Research
At Alcanza℠, we believe in the power of clinical research to move healthcare forward for all patients. Because research is the first step in bringing approved treatments to market, we encourage everyone to learn more about participating.