Clinical Research Coordinator

Job Summary:    

IMA Clinical Research is seeking an experienced Clinical Research Coordinator with proficiency in managing clinical trials and a background in phlebotomy. They are eagerly seeking individuals like you to become an integral part of our team in St. Petersburg, FL!    

As a Clinical Research Coordinator, you will be responsible for orchestrating and overseeing clinical trials in accordance with FDA requirements and GCP guidelines.    

Responsibilities:    

• Coordinating clinical trials according to sponsor protocols and ensuring adherence to SOPs.
• Acquiring and maintaining comprehensive knowledge of study protocols and associated procedures.
• Effectively communicating with various stakeholders within the research industry, including sponsors, CROs, monitors CRAs, IRBs, laboratories, and clinical personnel.
• Advising Investigator and staff on protocols and procedures essential for successful study implementation and completion.
• Timely notification of adverse events or serious adverse events as per the protocol.
• Upholding ALCOA principles for accurate and timely documentation, including meticulous data entry.

Education and Experience:    

• Preferably clinical experience in healthcare settings.
• Proficient in conducting and interpreting clinical and diagnostic tests (such as vital signs, height, weight, temperature, etc.) preferred.
• Capable of independent work, leading studies, and making informed decisions.
• Strong team player with proactive problem-solving skills.
• Exceptional communication, professional demeanor, and high motivation.

Qualifications:    

• At least two years of clinical research and phlebotomy experience.
• Preferred Clinical Research Coordinator certification (CCRC).
• Bilingual in English and Spanish is preferred.
• Proficient in leading multiple concurrent projects.
• Bachelor's degree required; significant demonstrated experience or a master’s degree is preferred.