Sara O'Neal Email & Phone Number

Hurdle Mills, Nc, Us

Hurdle Mills, Nc, Us

East Rutherford, New Jersey, Us

Analytical research and development in Early Stage Development and Testing

Monroeville, Pa, Us

Project manager for GLP investigative (non-regulatory) studies from initial proposal through report delivery.

Monroeville, Pa, Us

Technical data analyst responsible for interpretation and reporting of data supporting regulatory andinvestigative biomedical device studies under ISO 9001 and ISO/IEC 17025.

Roxboro, North Carolina, Us

Analytical support for raw material production, product development, finished goods, and cannabinoid research.

Research Triangle Park, Nc, Us

Analytical chemist in the DMPK division of Analytical Chemistry and Pharmaceutics working on internal, external, and federal projects.

Guildford, Surrey, Gb

Bioanalytical chemist at a CRO providing topical pharmaceutical development solutions for a dynamic range of commercial clients. Provided analytical support for formulation performance testing via high-throughput LC-MS/MS analysis. Developed and validated methods for detection of experimental and approved small-molecule drug compounds. Validated and conducted regulated bioequivalence studies under GLP and European EMA regulations.

Leverkusen, North Rhine-Westphalia, De

Principal bench chemist evaluating formulations, both in development and released, via HPLC. Included GLP studies and validations.

Us

Bioanalytical chemist on the metabolomics team at the Duke Molecular Physiology Institute. Primary scientist responsible for processing and analysis of biological pre-clinical and clinical samples on two Agilent GC-MS systems for non-targeted metabolomics and assisted with high-resolution/accurate-mass MS projects on Thermo QExactive+ Orbitrap HPLC-MS system.

Chapel Hill, Nc, Us

Laboratory manager for the Translational Oncology and Nanoparticle Drug Development Initiative Laboratory in the UNC Eshelman School of Pharmacy. Maintained active training in GLP, HIPAA policies, and human subjects training (CITI Group 1: Biomedical). Completed internal professional development training on project management in March 2015.

Chapel Hill, Nc, Us

Contributing bioanalytical chemist in the Analytical Chemistry and Pharmacology Core Facility (ACPCF) for the UNC Lineberger Comprehensive Cancer Center (LCCC). Developed and validated non-GLP LC/MS and LC/MS/MS methods to evaluate nanoparticle-based chemotherapeutic drugs for samples ranging from formulations in development to biological samples from pre-clinical and clinical studies. Independently coordinated pre-clinical murine studies in collaboration with LCCC Animal Studies Core.

Amsterdam, Nederland, Nl

Indoor Environmental Management Branch of the Air Pollution Prevention and Control Division. Sole ARCADIS scientist responsible for analysis and laboratory maintenance for project analyzing PFCs (perfluorinated compounds) in consumer products (woven and non-woven fabrics, liquids, etc.). LC/MS/MS analysis, report writing, sample and supply inventory management, instrumentation maintenance.

Amsterdam, Nederland, Nl

Decontamination and Consequence Management Division of the National Homeland Security Research Center. Contributed to research into low-tech strategies for anthrax decontamination from building surfaces. Trained on a range of respirator types and full-body personal protective equipment. Proficient in quantitative air sampling and analysis, aseptic processing techniques, and qualitative microbiological analysis.

Raleigh, North Carolina, Us

Solely responsible for lecture and lab instruction for 4 sections of general chemistry I. Proficient in theoretical knowledge and practical laboratory application of chemical sciences. Adept at multi-tasking, interacting with a wide variety of students and staff, and quickly resolving interpersonal and professional problems.

Research Triangle Park, Nc, Us

Developed and applied analytical methods for drug formulations and commercial products using HPLC and UHPLC, including raw material, bulk, final product, and stability testing. Responsible for method development and transfer using USP methods. Conducted all activities according to FDA cGMP and GLP regulations.

Raleigh, North Carolina, Us

Ba Magna Cum Laude, Chemistry, Minor In Women'S Studies

Ms, Analytical Chemistry