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Performs duties associated with research protocol kit construction and delivery, inventory, and destruction management/storage.
Refer to laboratory manuals and/or protocols as needed to confirm protocol kit construction and labeling. Reviews inventory for each protocol for accuracy and consistencies, notifies CRC of any changes to inventory threshold, shipments, and on-site availability. Work collaboratively with other CRA Kit Team members, Clinical Research
Coordinators, Data CRAs, and processing laboratory facilities.
Submit all constructed protocol kit for internal quality assurance reviews before delivery.
Deliver protocol kits to appropriate locations in a timely manner.
Update protocol kit inventory management tools in a timely manner.
Resolves or assists with issues regarding inventory space allocation, locating deliveries, and updating inventory databases in a timely manner by communicating with the primary CRC and/or disease group and all processing laboratories.
Suggests improved methods for accomplishing clinical research goals.
Maintains established departmental policies and procedures, objectives, quality assurance programs, safety, and compliance standards.
Enhances professional growth and development by participating in educational programs, reading current literature and participation in in-service meetings and workshops.
Prepares other written documentation as required by the profession and the department; maintains, distributes, analyzes, and projects information for required record, reports and statistics as directed.
Attends meetings as required, responses to emails and Microsoft Teams communications in a timely manner.
The pay range for this position is $53,357 – $67,810 annually which includes a comprehensive benefits package. The listed pay range reflects the range of potential compensation for this role. The actual offer may vary based on qualifications, skills, and experience.
