Clinical Research Pharmacy Technician (Unblinded CRC)

Dm Clinical Research Group; New York (NY); On-site; USD 65,000 - 85,000; Full time

Job summary

DM Clinical Research Group in Brooklyn, NY seeks a Pharmacy Technician to join as a Unblinded CRC and dispense Investigational Products for clinical trials. The role requires 2+ years in clinical research and relevant certifications, with duties spanning dispensing, vitals, specimen collection, injections, and data accuracy.

The position emphasizes regulatory compliance, IP accountability, and collaboration with the PI and study team to ensure protocol adherence and patient safety.

Qualifications

• Associates degree or 2 years of coursework required.
• Bachelor's degree preferred when available.
• Secondary/Foreign Medical Graduate preferred.
• 2+ years clinical research experience required.
• 1+ year Clinical Research Coordinator experience, blinded or unblinded, required.

Responsibilities

• Compound and dispense prescribed IP per sponsor protocol.
• Measure vital signs and document medical histories.
• Collect blood, urine and other specimens for testing.
• Administer injections or vaccines and monitor adverse reactions.
• Provide consultative support on preparation and dosing of drugs.
• Run routine tests like EKGs and maintain medication records.
• Maintain IP accountability and storage documentation.
• Ensure site regulatory documents and certifications are up to date.

Skills

Computer proficiency

Communication skills

Time management

Bilingual Spanish

Education

Associates Degree or 2 years coursework

Bachelor's degree preferred

Secondary or Foreign Medical Graduate

Tools

CRIO system

Job description

DM Clinical Research Group in Brooklyn, NY seeks a Pharmacy Technician to join as a Unblinded CRC and dispense Investigational Products for clinical trials. The role requires 2+ years in clinical research and relevant certifications, with duties spanning dispensing, vitals, specimen collection, injections, and data accuracy.

The position emphasizes regulatory compliance, IP accountability, and collaboration with the PI and study team to ensure protocol adherence and patient safety.