Tiffany Palmer Email & Phone Number
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Tiffany Palmer is listed as Associate Director Business Development DP and C at Pharmaron, a with 2049 employees, based in North Reading, Massachusetts, United States. AeroLeads shows a matched LinkedIn profile for Tiffany Palmer.
Tiffany Palmer previously worked as Principal Scientist Cardiovascular, Pulmonary, Metabolic & Rare Disease at Moderna and Sr. Scientist Drug Metabolism Pharmacokinetics at Moderna Therapeutics. Tiffany Palmer holds Master’S Degree, Biotechnology And Biomedical Science from University Of Massachusetts Boston.
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About Tiffany Palmer
I am a highly skilled and accomplished Pharmaceutical Biochemist with over two decades of experience in the pharmaceutical industry. My expertise lies in the specialized field of protein enzymology, assay development, drug metabolism, and pharmacokinetic evaluation of small molecules and mRNA. For the last 8 years of my career, I have been dedicated to developing transformative mRNA-medicines for cardiovascular, metabolic, and rare diseases, successfully navigating the entire drug development process from Target Identification to Investigational New Drug (IND) stages. In this role, I've not only excelled in my scientific contributions but also in managing and promoting team members, leveraging my exceptional proficiency in collaborating with external collaborators and Contract Research Organizations (CROs) to develop in vivo studies and facilitate assay transfers for discovery and development programs. One of my key strengths is my ability to foster effective collaboration and communication within multidisciplinary teams. I have consistently been recognized for my exceptional collaboration, communication, and community-building skills, which have been acknowledged through multiple corporate-level awards and annual performance evaluations.
Listed skills include Enzyme Kinetics, Enzyme Activity, High Throughput Screening, In Vitro, and 21 others.
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Tiffany Palmer work experience
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Principal Scientist Cardiovascular, Pulmonary, Metabolic & Rare Disease
• Spearheaded the innovative design and development of cutting-edge mRNA constructs aimed at addressing acute and chronic medical challenges, including Familial Hypertriglyceridemia (FTG), Type 2 Diabetes, Non-Alcoholic Steatohepatitis (NASH), Non-Alcoholic Fatty Liver Disease (NAFLD), cardiac dysfunction, and Rare Diseases.• Program leadership and collaborative expertise1. Led two pivotal internal programs, driving the discovery and identification of Lipid Nanoparticle (LNP) encapsulated mRNA formulations with a profound focus on delivery to Hematopoietic Stem and Progenitor Cells (HSPCs). Collaboratively pioneered the utilization of the "humanized NOG" mouse model from Taconic, revolutionizing the assessment of LNP-based therapies.2. Pioneered the identification of a novel animal model, positioned as a groundbreaking alternative to Non-Human Primates (NHPs), for the comprehensive study of LNP encapsulated mRNA biodistribution and expression profiles. This innovation significantly enhanced efficiency and ethical considerations in biodistribution studies.• Provided pivotal support to an array of internal Rare Disease pre-clinical and clinical programs, encompassing Relaxin, VEGF-A, MMA, OTC, PKU, and PA. Notably, played a critical role in refining study designs and conducting meticulous data analyses that substantially bolstered Investigational New Drug (IND) application preparations.
Sr. Scientist Drug Metabolism Pharmacokinetics
• Managed bioanalytical group: Developed internal assays to support Pre-clinical, Clinical and internal platform Studies.• Designed in vivo and in vitro ADME assays for mRNA Drug product and delivery system to support IND filings.• Toxicology project lead on 1 vaccine program and 1 rare disease programo Designed in vivo tox studies to support Development programs to determine the NOAEL to support IND filing• DMPK project lead on 2 Rare Disease programs. o Worked with Toxicologists developing IND supporting studies.o Worked with CMC to deliver Drug product to CRO’s for validation and assay qualification prior to study start.
Scientist, Drug Metabolism Pharmacokinetics
Senior Scientist
•Managed, trained and supported Global compound design and ordering system.•Performed detailed scientific Mode of Inhibition studies on novel bacterial topoisomerase inhibitor AZD0914 to support Phase II Clinical progression. Presented these results at the annual international Infection conference, ICAAC 2014.•Supported Phase I and Phase II Clinical Project: Detailed Mechanistic studies on novel DNA gyrase inhibitor AZD0914 (Phase1), in vitro target profiling for beta-lactamase inhibitor Avibactam (11 enzyme panel) that supported regulatory documentation for Phase II progression.•Developed and revised the standard operating procedures (SOPs) for radiation work, resulting in a decrease in experimental errors and increase in laboratory safety, health and environment.•Implemented an Infection-wide independent summer intern research program and developed successful research proposals for two summer intern students that resulted in contributions to two drug discovery programs.
Scientist
•Selected Lead for Infection BioScience representative for the department that aided in creating the design, implementation and training for a global compound design and ordering system. Utilized by all scientist globally, enabling them to work more efficiently by streamlining compound ordering and testing.•Analyzed and characterized multiple early-stage drug discovery targets, from various metabolic pathways.•Enabled project transitions across drug discovery process through Hit Evaluation, Lead Optimization, including Lead Identification.•Performed detailed Mechanism of Inhibition studies with Beta-lactamase inhibitors, topoisomerases, and many others.•Selected as representative, In-lab expert on Safety, Health and Environment subject matters including hazard waste disposal, PPE and training requirements and orient new employee to laboratory specifics of site and safety policy.•Organized summer internship program and engagement seminars for enabling summer student to learn about all aspects of early and late drug discovery, end of internship participants internally presented a poster and/or presentation about work.
Senior Associate Scientist
•Developed and validated a filtration assay that monitored the effect of potential drug candidate’s ability to bind to the human ether-a-go-go (hERG) ion channel to expedite decisions around compound series and aide in building structure activity relationship.•Created standard operating procedures (SOPs) for high-throughput screening and hit evaluation follow-up.•Designed and transferred of enzymatic assay locally and globally – assess customer capabilities and requirements, and performed basic statistical analysis of data.•Enabled several project transitions across drug discovery process from Hit Evaluation, to Lead Optimization, and finally to Lead Identification.•Selected as in-lab expert on Radiation Safety – Monitored, maintained and trained laboratory individuals on our site isotope requirements, protection, and usage.
Research Associate
•Design, execution, and analysis of In vitro dose response experiments•Biophysical characterization of enzymes including assay development (optimization of reaction conditions vary salt, buffer, temperature, surfactants)
Lab Technician Ii
•Managed laboratory notebooks and maintained laboratory SOP’s for undergraduate and graduate research students•Aided in graduate and undergraduate research work; cell culture, western blotting, cloning, protein purification, quantification and storage, as well as making protein and DNA gels for routine analysis. •Maintained laboratory equipment, cleaning and calibration of microscopes, scales, pH meters, and pipettes•Prepared reagents and buffers according to Laboratory SOP for general usage•Organized laboratory inventory, purchased and maintained general reagent stocks
Colleagues at Pharmaron
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Joseph Barker
Colleague at PharmaronGreater Bristol Area, United Kingdom
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Katherine Roberts
Colleague at PharmaronBirkenhead, England, United Kingdom
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Tony Cruise
Colleague at PharmaronUnited Kingdom
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Max Blomberg
Colleague at PharmaronBaltimore, Maryland, United States
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Simon Pill
Colleague at PharmaronGreater Cheshire West And Chester Area, United Kingdom
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Latoya Washington
Colleague at PharmaronBaltimore, Maryland, United States
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Michelle Richards
Colleague at PharmaronLouisville, Kentucky, United States
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Kimberly Blair
Colleague at PharmaronOwings Mills, Maryland, United States
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Giancarlo Vallejo
Colleague at PharmaronSan Diego, California, United States
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Wang Yulong
Colleague at PharmaronChina
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Tiffany Palmer education
Master’S Degree, Biotechnology And Biomedical Science
Bachelor’S Degree, Biochemistry
Education record
Frequently asked questions about Tiffany Palmer
Quick answers generated from the profile data available on this page.
What company does Tiffany Palmer work for?
Tiffany Palmer works for Pharmaron.
What is Tiffany Palmer's role at Pharmaron?
Tiffany Palmer is listed as Associate Director Business Development DP and C at Pharmaron.
Where is Tiffany Palmer based?
Tiffany Palmer is based in North Reading, Massachusetts, United States while working with Pharmaron.
What companies has Tiffany Palmer worked for?
Tiffany Palmer has worked for Pharmaron, Moderna, Moderna Therapeutics, Astrazeneca, and University Of Massachusetts.
Who are Tiffany Palmer's colleagues at Pharmaron?
Tiffany Palmer's colleagues at Pharmaron include Joseph Barker, Katherine Roberts, Tony Cruise, Max Blomberg, and Simon Pill.
How can I contact Tiffany Palmer?
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What schools did Tiffany Palmer attend?
Tiffany Palmer holds Master’S Degree, Biotechnology And Biomedical Science from University Of Massachusetts Boston.
What skills is Tiffany Palmer known for?
Tiffany Palmer is listed with skills including Enzyme Kinetics, Enzyme Activity, High Throughput Screening, In Vitro, Assay Development, Internships, Enzyme Assays, and Drug Discovery.
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