Clinical Research Assistant: Frontline in CNS Trials

Ergclinical; Miami, Northern (FL, KY); Hybrid; USD 30,000 - 37,000; Full time

Benefits offered by this job

Medical and dental coverage

401(k) matching

Paid time off

Job summary

Evolution Research Group (ERG) is seeking an Assistant Clinical Research Coordinator to support ongoing clinical trials at our CPMI-Clinical Pharmacology Miami site. The role involves coordinated data collection, patient interactions, and adherence to study protocols in a fast-paced environment.

Responsibilities include assisting coordination, informed consent administration, and ensuring study procedures meet regulatory requirements while maintaining participant comfort and safety.

Qualifications

• Maintains licensure, registration and/or certification within educational background.
• Maintains current BLS and/or ACLS certification.
• Maintains necessary CEU’s for licensure, registration and/or certification.
• Keeps apprised of HIPAA and Compliance Programs and CPMI policies.

Responsibilities

• Monitor and ensure study data is collected following plan of care and guidelines.
• Serve in rotation with assistant coordinators and coordinators.
• Liaise between clinical research coordinator and departments.
• Discuss and administer Informed Consent Form.
• Set up supplies and equipment per protocol.
• Assist with study schedules and flowsheets to meet protocol requirements.
• Perform venipuncture, vital signs, ECG and other assessments.
• Provide high-quality care under pressure.

Education

Licensure/Certification

BLS/ACLS certification

CEUs for licensure

HIPAA and Compliance knowledge

Tools

EKG machines

Holter monitoring

Job description

Evolution Research Group (ERG) is seeking an Assistant Clinical Research Coordinator to support ongoing clinical trials at our CPMI-Clinical Pharmacology Miami site. The role involves coordinated data collection, patient interactions, and adherence to study protocols in a fast-paced environment.

Responsibilities include assisting coordination, informed consent administration, and ensuring study procedures meet regulatory requirements while maintaining participant comfort and safety.