Overview

We’re looking for a detail-oriented Research Pharmacy Technician to support clinical trials by managing investigational products (IP) and ensuring everything runs smoothly, safely, and in full compliance with study protocols and regulations. This role is ideal for someone who thrives in a fast-paced research environment and takes pride in precision and teamwork.

Key Responsibilities

• Ensure all investigational product (IP) activities comply with study protocols, FDA regulations, and institutional SOPs
• Receive, handle, store, track, and dispense investigational products accurately
• Maintain real-time IP accountability logs and temperature monitoring records
• Verify study materials, documentation, and data for accuracy and regulatory compliance
• Perform aseptic preparations (reconstitution, dilution, and compounding) with a high level of precision and adherence to sterile technique
• Maintain proper storage conditions and ensure study supplies are always ready
• Document all processes thoroughly in accordance with clinical and regulatory standards
• Enter and manage IP-related data in CTMS and sponsor systems (EDC, IVRS/IWRS)
• Work closely with the research team and communicate proactively to support daily operations
• Assist with monitoring visits, audits, and regulatory inspections, especially related to IP accountability
• Support equipment maintenance and respond to environmental monitoring alerts as needed
• Contribute to team training and continuous improvement efforts

Qualifications

• At least 1 year of experience in clinical research, pharmacy, or a related healthcare setting
• Strong hands-on experience with aseptic preparation
• Active Florida Pharmacy Technician license (required at onboarding)
• National certification (e.g., PTCB) is preferred but not required
• Working knowledge of FDA regulations, ICH-GCP, and IRB processes
• Experience with investigational product (IP) management in clinical trials
• Familiarity with IVRS/IWRS systems and electronic data capture platforms
• Proficient in Microsoft Word and Excel
• Strong organizational skills with the ability to manage multiple studies simultaneously
• Experience in a clinical research or regulatory environment is a strong plus
• Bilingual (English/Spanish) preferred

Work Environment

• Fully on-site position

• Collaborative healthcare office environment

• Regular use of computer systems and documentation review

Schedule

Full-time | Monday – Friday
Minimum 40 hours per week
Pay range $20-$22 per hour

Benefits include:

• Health Insurance

• Dental Insurance

• Vision Insurance

• 401(k)

• Flexible Spending Account (FSA)

• Paid Time Off

• Professional development opportunities

If you are passionate about improving healthcare quality and ensuring compliance standards are met, we encourage you to apply and become part of our team.

People with a criminal record are encouraged to apply

Work Location: In person

This description indicates, in general terms, the type and level of work performed and responsibilities held by the team member(s).  Duties described are not to be interpreted as being all-inclusive or specific to any individual team member.  

No Third Party Agencies or Submissions Will Be Accepted.  

Our company is committed to creating a diverse environment. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status. DFWP  

Opportunities posted here do not create any implied or express employment contract between you and our company / our clients and can be changed at our discretion and / or the discretion of our clients. Any and all information may change without notice. We reserve the right to solely determine applicant suitability. By your submission you agree to all terms herein.