Pharmacy Technician (4122)

DM Clinical; New York (NY); On-site; USD 45,000 - 65,000; Full time

Job summary

DM Clinical Research is seeking a Pharmacy Technician to join our team as an Unblinded CRC. The role involves dispensing Investigational Products (IP) and supporting trial operations per sponsor-approved protocols.

Responsibilities include dispensing IP, taking vital signs, collecting specimens, administering injections where appropriate, and ensuring regulatory documents and IP accountability are maintained in up-to-date condition. Strong communication and bilingual skills are preferred.

Qualifications

• Associates degree or 2 years of formal coursework required.
• Bachelor’s degree preferred.
• Secondary or foreign medical graduate preferred.

Responsibilities

• Compound and dispense Investigational Products per 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 prep and dosing of drugs.
• Run routine tests like EKGs.
• Maintain records of all medications and IP accountability.
• Ensure regulatory documents and site certifications are up to date.
• Interact with PI, sponsor, and study staff to ensure protocol compliance.

Skills

Communication

Time management

Bilingual Spanish

Education

Associates degree

Bachelor’s degree preferred

Foreign medical graduate preferred

Tools

CRIO

Job description

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