Job Description

Job Description: Maintain and manage inventory of GLP and Clinical bioanalytical samples and critical reagents • Utilize LIMS to track sample chain of custody from receipt through disposal/shipping • Coordinate domestic and international sample or reagent shipments off-site • Retrieve and provide materials to bioanalytical staff on site • Perform aliquoting of clinical samples either through manual pipetting or lab automation • Utilize electronic laboratory notebooks for laboratory documentation • Communicate with clinical sites, central lab, or on-site collection areas for receipt of materials and discrepancy resolution • Participate in CTU maintenance and alarm handling • Follow and help develop local SOPs for sample management processes • Participate in and/or lead process improvement efforts • Demonstrate personal commitment with respect to working safely, healthy and environmentally friendly.

Responsibilities: Maintain and manage inventory of GLP and Clinical bioanalytical samples and critical reagents • Utilize LIMS to track sample chain of custody from receipt through disposal/shipping • Coordinate domestic and international sample or reagent shipments off-site • Retrieve and provide materials to bioanalytical staff on site • Perform aliquoting of clinical samples either through manual pipetting or lab automation • Utilize electronic laboratory notebooks for laboratory documentation • Communicate with clinical sites, central lab, or on-site collection areas for receipt of materials and discrepancy resolution • Participate in CTU maintenance and alarm handling • Follow and help develop local SOPs for sample management processes • Participate in and/or lead process improvement efforts • Demonstrate personal commitment with respect to working safely, healthy and environmentally friendly.

Qualifications: Educational background at a minimum - Associate's Degree in the sciences or related field with 4yrs in the pharmaceutical or related industry / Bachelor's Degree in the sciences or related field with minimum of 2 years in the pharmaceutical or related industry • Strong knowledge in GxP and compliance guidelines, preferably in a bioanalytical laboratory environment • Experience managing sample chain of custody within a GLP/GMP lab • Computer literacy knowledge (e.g. MS Office) and experience using a laboratory LIMS system (e.g. WatsonLIMS, LabwareLIMS, etc) • Ability to work under minimum supervision • Team work oriented • Strong interpersonal and communication skills, oral and written. Must be able to lift at least 25lbs. Required: Candidate must have prior experience with sample management / sample processing activities, and running assays.