Job Description

The Sr. Clinical Research Coordinator will be responsible for overseeing and managing clinical research studies, ensuring compliance with protocols, obtaining informed consent, and coordinating clinical trials. The role involves collaboration with investigators, research staff, and participants to ensure the successful execution of research projects. Additionally, the coordinator will maintain accurate and detailed records, adhere to regulatory requirements, and manage study documentation.

Qualifications

• Experience with Informed Consent and Protocol adherence
• Clinical Research Experience and ability to conduct Research
• Knowledge and experience in managing Clinical Trials
• Strong organizational and time management skills
• Excellent written and verbal communication skills
• Ability to work collaboratively with a research team
• Bachelor's degree in a related field; advanced degree or certification in clinical research is a plus

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