David Benedict

About David Benedict

I am a highly dedicated and committed Study Supervisor with 15+ years of experience in…

Experience

1. Supervisor, Research Associate

   Altasciences

   Apr 2021 — Present

   Supervise animal technical research team, focusing on surgical, swine and other general toxicological studies. • Train and mentor study supervisors in scheduling and data management practices. • Create/revise SOPs, procedures, training plans, and facility processes. • Ensure staff maintains Good Laboratory Practices (GLP). • Ensure staff have proper training, supplies, and support to carry out In-Life phases of study designs. • Overseeing Pre-clinical in vivo GLP and non-GLP studies. • Performing Quality Assurance audits on data collected in GLP research studies. • Assisting in drafting study protocols and coordinating workflow across multiple departments.

Skills

• Good Laboratory Practice (Glp)
• Quality Assurance Audits
• Data Analysis
• Validation
• Polymerase Chain Reaction (Pcr)
• In Vivo Research
• Biotechnology
• Level 2 Biosafety Environment
• Real-Time Polymerase Chain Reaction (Qpcr)
• Microbiology
• CRO Management
• Laboratory
• Dna Sequencing
• Laboratory Knowledge
• Pharmaceutical Research
• In Vivo
• Laboratory Skills
• Sop Authoring
• Glp Regulations
• Sop
• Standard Operating Procedure (Sop)
• Lims
• Sequencing
• Data Collection
• Bacterial Samples & Specimens
• Pharmaceutical Industry
• Clinical Development
• Glp
• Dna
• Dna/Rna Extraction
• Molecular Biology
• Laboratory Information Management System (Lims)
• Self-Directed
• U.s. Food and Drug Administration (Fda)
• Assay Development
• Qpcr
• Life Sciences
• Quality Control
• Pcr
• Work with Mice & Rats