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Pharmacy Technician - Clinical Trial Assistant; Hybrid

Job in Chesterfield, St. Louis County, Missouri, 63005, USA
Listing for: EVERSANA
Full Time position
Listed on 2026-01-12
Job specializations:
  • Healthcare
    Pharmacy Technician, Medical Technologist & Lab Technician
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below
Pharmacy Technician - Clinical Trial Assistant (Hybrid)

At EVERSANA, we are proud to be certified as a Great Place to Work across the globe. We’re fueled by our vision to create a healthier world. Our global team of more than 7,000 employees is committed to creating and delivering next-generation commercialization services to the life sciences industry. We serve more than 650 clients ranging from innovative biotech start-ups to established pharmaceutical companies.

Our products, services, and solutions help bring innovative therapies to market and support the patients who depend on them.

Across our growing organization, we embrace diversity in backgrounds and experiences. Improving patient lives around the world is a priority, and we need people from all backgrounds to help build the future of healthcare and the life sciences industry. We believe our people make all the difference in cultivating an inclusive culture.

Job Description

The Clinical Trial Assistant (CTA) supports clinical trials by maintaining organized files, performing pharmacy technician duties, and communicating routinely with trial sites, coordinators, and patients while demonstrating good clinical practices and following standard operating procedures.

Essential Duties And Responsibilities
  • Monitor study activities to ensure compliance with protocols and all relevant local, federal, and state regulatory and institutional policies.
  • Maintain required records of study activity including case report forms, drug dispensation records, and regulatory forms.
  • Order drugs or devices necessary for study completion.
  • Maintain current knowledge of clinical studies affairs and issues by reviewing scientific literature, participating in continuing education activities, and attending conferences and seminars.
  • Prepare for and participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.
  • Organize space for study equipment and supplies.
  • Participate in the development of study protocols including guidelines for administration or data collection procedures.
  • Maintain contact with sponsors to schedule and coordinate site visits or to answer questions about issues such as incomplete data.
  • Identify protocol problems, inform investigators of problems, and assist in problem resolution efforts such as protocol revisions.
  • Dispense medical devices or drugs and calculate dosages and provide instructions as necessary.
  • Successful fulfillment and delivery of all prescriptions and supplies to patients in a timely manner.
  • Management of medication and supply inventory.
  • Positive patient and client experience throughout the entire patient journey.
  • All other duties as assigned.
  • Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position.
Expectations Of The Job
  • To understand, organize and archive clinical trial documents, including study protocols, SOPs, Resource Documents, dispensing and manufacturing records, email correspondence, training materials and other study documents.
  • Maintain current lists of correspondence.
  • Administer clinical trials according to good clinical practices and standard operating procedures.
  • Provide general logistical support for clinical trials by entering subject and study site orders and arranging and confirming deliveries of study medications and supplies.
  • Pick and pack patient prescriptions, wholesale orders, and supply orders.
  • Inspect on-hand inventory for integrity, purity, and appropriate expiration dating.
  • Ensure all manufacturer program specific literature and materials are included in shipments as necessary.
  • Create and ensure appropriate third party shipping labels are attached to all patient prescriptions, wholesale orders, and supply orders.
  • Restock medication, supply, and ancillary products upon receipt.
  • Keep all medications and ancillary supplies organized, rotated by expiration date and sorted by lot number.
  • Assist with shipment status modification (i.e. hold, return-to-stock).
  • Participate in all medication and supply inventories as assigned.
  • Compliance with all applicable state and federal pharmacy laws.
  • Some travel may be…
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