Scientist Ii Resume Example
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(555) 432-1000 - - resumesample@example.com - -
Determined and well-rounded individual with more than 40 years working as Scientist within pharmaceutical industry. Sharp and focused professional offering skills in Preclinical Safety. Recognized consistently for collaboration across team labs and building new network connections within existing project teams.
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- Conducts in vivo, postmortem and laboratory aspects of non-GLP preclinical safety studies in various laboratory animal species.
- Performs all technical procedures necessary to implement and conduct study protocols for safety evaluation studies with no supervision.
- Documented changes during experiments, noting unexpected issues arising during research activities.
- Prioritized project tasks after discussions with Laboratory Sciences department team.
- Simultaneously managed several complex projects, meeting all pertinent milestones. Used coordination and planning skills to achieve results according to schedule.
- Knows and conforms to GLPs, Novartis SOPs, policies, standards, requirements, and guidelines.
- May perform (with minimal or no supervision) activities such as: clinical laboratory analyses (i.e. Hematology, chemistry, coagulation, flow cytometry, urinalysis, microscopy, QC activities, study monitoring, etc.), producing toxicity information, data reporting and/or interpretation, instrument and assay qualification, and clinical pathology reports.
- Provide quality testing and result verification while displaying good scientific judgement.
- Communicate results and interpretations in accurate and timely manner.
- Will function on teams and/or lead teams assigned to major activities.
- Display high level of competence in use of laboratory equipment with experience in detailed maintenance and troubleshooting when required.
- Work independently to resolve issues.
- Manage 100% department purchasing and instrument contracts
- Contributor study monitor for outsourced laboratory tests
- Knows and conforms to GLPs, Novartis SOPs, policies, standards, requirements, and guidelines.
- May perform (with minimal or no supervision) activities such as: clinical laboratory analyses (i.e. Hematology, chemistry, coagulation, flow cytometry, urinalysis, microscopy, QC activities, study monitoring, etc.), producing toxicity information, data reporting and/or interpretation, instrument and assay qualification, and clinical pathology reports.
- Provide quality testing and result verification while displaying good scientific judgement.
- Communicate results and interpretations in accurate and timely manner.
- Will function on teams and/or lead teams assigned to major activities.
- Display high level of competence in use of laboratory equipment with experience in detailed maintenance and troubleshooting when required.
- Work independently to resolve issues.
- Contributor study monitor for outsourced laboratory tests
- In conformance with all SOPs GLPs, Safety and Novartis safety regulations, perform activities such as: clinical laboratory analyses (i.e. Hematology, chemistry, coagulation, flow cytometry, urinalysis, microscopy, QC activities, etc), producing toxicity information and data interpretation.
- Provide quality testing and result verification while displaying good scientific judgment.
- Communicate results and interpretations accurately and on or before established timelines.
- Display high level of competence in use of all laboratory equipment.
- Perform technical procedures necessary to implement and conduct study protocols for safety evaluation studies.
- Responsible for training less experienced personnel.
- Troubleshoot equipment problems.
- Responsible for department scheduling of laboratory work with Toxicology, Pathology, Research and other areas (i.e. Cambridge, Basel).
- Represent Clinical Pathology at all protocol initiation meetings.
- Provide methods and references for all protocols associated with Clinical Pathology.
- Assist with SOP processes and quality assurance of Clinical Pathology data.
- Contributor Study Monitor for Clinical Pathology tests outsourced to contract lab facilities.
University Of Phoenix - Tempe, AZ
Central Carolina Community College - Sanford, NC,
American Association of Clinical Chemistry (DACC)
PUBLICATIONS:
The effect of PAXgene TM RNA stablizer contamination on clinical pathology results in canine blood samples, k. Hart, J. DeMario, L. Yanas, E. Skuba. Novartis Pharmaceuticals Corporation, East Hanover, N.J.
Genetic analysis of albuminuria in Collaborative Cross and multiple mouse intercross populations, Jill Thaisz, Shirng-Wern Tsaih, Minjie Feng, Vivek Philip, Liane Yanas, Susan Sheehan, Lingfei Xu Beverly Paigen, Elissa Chesler, Gary A. Churchill, and Keith DiPetrillo.
Novartis Institutes for BioMedical Research & Novartis Pharmaceuticals Corp., East Hanover, NJ 07936, The Jackson Laboratory, Bar Harbor, ME 04609, Oak Ridge National Laboratory, Oak Ridge, TN 37831
Genome-Wide Assocaition Mapping of Quantitive Traits in Outbred Mice, Weidong Zhang, Ron Korstanje, Jill Thaisz, Frank Staedtler, Nicole Harttman, Lingfei Xu, Minjie Feng, Liane Yanas, Hyana Yang, William Valdar, Gary A. Churchhill and Keith DiPetrillo.
Acknowledgments and technical assistance for the publication of: The tolerability and pharmacology of interleukin-6 administered in combination with GM-CSF or G-CSF in the rhesus monkey, Myers LA, Boyce JT, Robison RL
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Resume Overview
- University Of Phoenix
- Central Carolina Community College
- Scientist II
- Scientist II
- Senior Scientist
- Scientist, Safety Profiling and Assessment
- Bachelor of Science
- Associate of Applied Science