University of Rochester Clinical Trials Production Technician - 228578 in Rochester, New York
Clinical Trials Production Technician Job ID 228578Location School of Medicine & Dentistry Full/Part Time Full-Time Favorite Job Regular/Temporary Regular Opening
Full Time 40 hours Grade 092 Path & Lab Clinical TrialsResponsibilities
Under direction from the Clinical Trials Production Coordinator and Department Manager, and with some latitude for independent judgment, supports daily activities ensuring that investigator sites have adequate and appropriate materials to collect specimens for multi-center clinical trials and internal clinical research projects for the clinical trials central laboratory (CTCL) . Design and produce forms and labels, assemble and ship materials, and perform general clerical functions to support to CTCL staff and clinical trials and research projects . Follows project specifications and communicates kit related information to internal and external customers. Communicates roadblocks and identifies oppo1tunities for process improvement.
SUPERVISION AND DIRECTION RECEIVED:
Receives direction from the Clinical Production Coordinator or the Department Manager.
SUPERVISION AND DIRECTION EXCERCISED:
MACHINES AND EQUIPMENT USED:
Standard office equipment such as multi-feature ACD telephone , PC, copier, printer , fax machine, and the like. Software systems such as Laboratory Info1mation Systems (LIS), databases such as MS Access, and various document design software applications.
Supports Implementation of Internal Research Studies and Clinical Trials . (40%)
Designs labels, forms, and worksheets required to identify samples submitted for testing.
Maintains investigator shipping information database.
Enters study specific materials requirements in the Logistics Materials database
Prepares and maintains customer files and documentation including custom study forms.
Prints and assembles lab instruction manuals.
Maintains inventory and ensures that investigator sites have adequate and appropriate materials and documentation to collect specimens for projects. (25%)
Enters and maintains accurate inventory information in the ClinAxys II laborato1y information system.
Reviews monthly reports for materials expiration
Prints labels and forms to study and visit specifications for customer orders
Collates laboratory specimen collection materials to study and visit specifications for customer orders
Packages specimen collection materials for shipment
Creates courier airway bills for domestic and international shipments. Compiles all necessary regulato1y and customs documentation for international shipments.
Supports daily operations for research studies and clinical trials (25%)
Communicates project indicators to internal management.
Enters client orders into kit production software
Produces documentation required to accurately bill for specimen collection kits
Answers telephone and e-mail inquiries from investigator sites regarding supply orders.
Tracks delive1y of outbound packages through FedEx.
Other duties and projects as assigned . (10%)
Ability to manage multiple competing priorities and projects.
Ability to interact effectively and professionally with co-workers, customers, and vendors.
Good computer and organizational skills.
Ability to adjust work schedule if needed to meet project timelines.
Adheres to all departmental and organizational policies and procedures.
Demonstrates all aspects of ICARE values.
AS and one (1) year laboratory experience preferred, or
Two (2) years Laboratory Science and technical training closely related to this position, or
A combination of formal training and experience equivalent to the above
Experience in laboratory research and familiarity with Laboratory Information Systems preferred.
How To Apply
All applicants must apply online.
EOE Minorities/Females/Protected Veterans/Disabled