Pharmacy Technician (4122)

Dm Clinical Research Group; New York (NY); On-site; USD 62,000 - 75,000; Full time

Job summary

DM Clinical Research in Brooklyn, NY seeks a Pharmacy Technician to join as an Unblinded CRC. You will dispense Investigational Products (IP) in clinical trials and support study protocols, reporting to the Principal Investigator and study team.

The role requires 2+ years in clinical research, with strong communication, data accuracy, and documentation skills. Proficiency in computer tools and Spanish language is valued.

Qualifications

• 2+ years of Clinical Research experience required.
• 1+ year of Clinical Research Coordinator experience, Blinded or Unblinded, required.
• 1+ year utilizing CRIO, preferred.
• LPN or CMA, preferred; Pharmacy Technician Certification, preferred.

Responsibilities

• Compound and dispense prescribed IP per protocol.
• Measure vital signs and document medical histories.
• Collect blood and other specimens for testing.
• Administer injections or vaccines and monitor for adverse reactions.
• Provide consultative support on drug preparation and dosing.
• Run routine tests like EKGs.
• Maintain records of all medications.
• Audit clinical data for completeness and accuracy.
• Ensure regulatory documents and site certifications are up to date.
• Maintain IP accountability and proper IP storage.

Skills

Communication skills

Time management

Bilingual Spanish

Computer proficiency

Education

Associates degree or 2 years coursework

Bachelor's degree preferred

Secondary or Foreign Medical Graduate preferred

Tools

CRIO

Job description

Job DetailsJob Location: Brooklyn, NY (AOM) - Brooklyn, NY 11220

Salary Range: $62,000.00 - $75,000.00 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

Qualifications