Registered Nurse (4122)

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

Job Details

Job Location: Brooklyn, NY (AOM) - Brooklyn, NY 11220, Salary Range: $65,000.00 - $85,000.00 Salary/year, DM Clinical Research is looking to hire an Pharmacy Technician to join our team and work as a Unblinded CRC to join our team. This individual will be responsible for dispensing Investigational Products (IP) as part of clinical research trials.

Duties & Responsibilities

• Compound and dispense prescribed IP as needed by Sponsor approved protocol
• Measure vital signs (blood pressure, pulse, temperature, weight) and document medical histories.
• Collect blood (phlebotomy), urine, and other specimens for testing.
• Administer injections or vaccines, and monitor patients for adverse reactions.
• Provide consultative support regarding the preparation and dosing of drugs
• Run routine tests like EKGs (electrocardiograms).
• Supervise and maintain records of all medications
• Perform regular audits on the clinical data to assess percent completeness and accuracy
• Ensure external sites’ regulatory documents and required site certifications are up to date
• Maintain documentation of IP accountability: receipt, dispensing, return to sponsor/destruction
• Ensure receipt and proper storage of IP and bioretention samples, including temperature reporting
• Interact with Principal Investigator, sponsor, study manager and other study coordinators to ensure all aspects of protocols and study requirements are understood.

KNOWLEDGE & EXPERIENCE

Education

• Associates Degree required or 2 years of formal educational coursework
• Bachelor's degree, preferred
• Secondary or Foreign Medical Graduate, preferred

Experience

• 2+ years of Clinical Research experience, inclusive of in-clinic experience, required
• 1+ year of Clinical Research Coordinator experience, Blinded or Unblinded, required
• 1+ year utilizing CRIO, preferred

Credentials

• LPN (Licensed Professional Nurse) or CMA (Certified Medical Assistant), preferred
• Pharmacy Technician Certification, preferred
• Completion of DMCR-required training, including GCP, OSHA and IATA

Knowledge and Skills

• Computer proficiency, especially Word, Excel, Outlook, and Google Suite products.
• Excellent communication and customer service skills, both written and verbal
• Excellent time-management skills
• Bilingual (Spanish) preferred