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Michael Poss Email & Phone Number

Senior Vice President, Peptide Chemistry at Syneron Bio
Location: Trenton, New Jersey, United States 15 work roles 2 schools
1 work email found @bms.com LinkedIn matched
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Role
Senior Vice President, Peptide Chemistry
Location
Trenton, New Jersey, United States

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Michael Poss is listed as Senior Vice President, Peptide Chemistry at Syneron Bio, based in Trenton, New Jersey, United States. AeroLeads shows a work email signal at bms.com and a matched LinkedIn profile for Michael Poss.

Michael Poss previously worked as Senior Vice President, Peptide Chemistry at Syneron Tech and Scientific Director - Millamolecular Chemistry at Bristol Myers Squibb. Michael Poss holds Doctor Of Philosophy - Phd, Organic Chemistry from University Of Rochester.

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About Michael Poss

Michael Poss currently is a Senior Vice President at Syneron Tech, an innovative peptide therapeutics company empowered by unique platforms and next generation AI capabilities. Prior to joining Syneron, he led a Millamolecular team at Bristol Myers Squibb. Over the course of 40 years, he has overseen efforts that have been part of full phase programs, Early Discovery Chemistry, Combinatorial Chemistry, Millamolecular Chemistry, and Process Development.Mike received his BS and PhD in Organic Chemistry from the University of Rochester. He began his career at Merck as a computational/bench chemist, and then moved to E.R. Squibb in 1986. The first two programs that he worked on included the antihypertensive targets renin and angiotensin II, which included Mike's identification of a development candidate for the AII program. In 1992, when presented with a new opportunity, Mike transitioned to the BMS Development organization where he led a group that worked on several projects including novel routes to produce taxol. These efforts led to a process to efficiently prepare taxol from baccatin III which was implemented to produce clinical supplies. Next, Mike returned to Discovery Chemistry to lead a group focused on applying automated synthesis to accelerate medicinal chemistry. This effort led to the identification of lomitapide, a novel inhibitor of microsomal triglyceride transfer protein (MTP). Lomitapide was the first BMS clinical candidate to be prepared initially via robotics, and Mike, together with the MTP team, were recipients of the ACS Heroes of Chemistry Award recognizing this effort. Lomitapide (Juxtapid™) was subsequently out-licensed and is currently prescribed to treat hypercholesterolemia. Following his work with automated synthesis, Mike assumed responsibility for the Early Discovery Chemistry group which advanced hit-to-lead SAR across the BMS discovery portfolio. Under his supervision, several different early phase programs were progressed to full phase that delivered clinical assets such as beclabuvir (HCV NS5B), deucravacitinib (TYK2), afimetoran (TLR7/8), and BMS-986158 (BRD4).Next, Mike engaged in the pioneering efforts of the BMS Millamolecular team, which leveraged selection technology to identify and advance cyclic peptides as therapeutics. Strategies were developed to chemically modify Milla peptides to optimize stability and PK, prepare drug conjugates, and incorporate PET tracers for imaging. From these efforts, three compounds were advanced into clinical development including two therapeutics and one PET imaging agent.

Listed skills include Pharmaceutical Industry, Drug Discovery, Drug Development, Clinical Development, and 14 others.

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Syneron Bio
Syneron Bio
Senior Vice President, Peptide Chemistry
Trenton, NJ, US
AeroLeads page
15 roles

Michael Poss work experience

A career timeline built from the work history available for this profile.

Senior Vice President, Peptide Chemistry

Syneron Bio

Trenton, Nj, Us

Senior Vice President, Peptide Chemistry

Current
Jul 2022 - Present

Scientific Director - Millamolecular Chemistry

Lawrence Township, Nj, Us

- Managed a chemistry group across two sites focused on the progression of linear and macrocyclic peptides as therapeutics, drug conjugates, and imaging agents.- Advanced three compounds into clinical development, two therapeutics and one PET agent.- Coordinated the development of new software to efficiently generate peptide sequences and structures, evaluate SAR, and propose new sequences combining productive mutations.- Led the adoption of new organizational processes to streamline the synthesis and purification of peptidic analogs for SAR optimization.- Directed the development of novel solid phase and solution phase chemistry to prepare and functionalize amino acids and advanced peptide intermediates.- Drove the implementation of new methodology and instrumentation to enable the large-scale synthesis of peptides and peptide intermediates.- Advanced the study of nanoparticles to improve peptide dissolution, cell permeability and oral bioavailability.- Managed several academic collaborations exploring topics such as peptide grafting, cell targeting, and the flash nanoprecipitation of peptides.- Managed numerous biotech collaborations exploring topics such as selection strategies to provide orally bioavailable peptides, and novel formulations to enhance peptide bioavailability.

Jan 2013 - Jul 2022

Director - Lawrenceville Early Discovery Chemistry

Lawrence Township, Nj, Us

- Managed a Hits to Leads chemistry group focused on the progression of immunology and oncology early phase programs.- In total, many different early phase efforts were progressed to full phase programs that subsequently delivered clinical assets such as beclabuvir (HCV NS5B), deucravacitinib (TYK2), afimetoran (TLR7/8 antagonist), and BMS-986158 (BRD4 inhibitor).- Established novel hardware and software for large scale library synthesis (1K to 5K compounds).- Directed the synthesis, purification, and characterization of 45,000 millamolecular analogs over the period of one year.- Managed an external academic collaboration exploring the in-situ cell-based biosynthesis and testing of genetically engineered peptide analogs.- Chaired the committee that prioritized the allocation of macromolecular resources (CADD, Protein Sciences, NMR, and X-ray) across all programs at the BMS Lawrenceville site.- Chaired the committee that coordinated HTS screens and resources for immunology and oncology programs at the BMS Lawrenceville site.

Jan 2009 - Dec 2012

Director - Early Discovery Chemistry

Lawrence Township, Nj, Us

- Managed three Hits to Leads chemistry groups totaling ~40 chemists across different sites that concurrently prosecuted ~10 different early phase programs.- Co-chaired the exploratory and early phase operating committee at the Lawrenceville site providing review and prioritization of immunology and oncology programs.- Chaired the committee that prioritized the allocation of macromolecular resources (CADD, Protein Sciences, NMR, and X-ray) across all programs at the BMS Lawrenceville site.- Advanced hit identification, validation, and optimization processes. Coordinated the establishment of significantly improved screening triage processes.- Advanced the definition of Program Readiness Criteria. Authored a corporate Program Readiness document that provided guidelines for programs to move from exploratory to early and full phases.

Jan 2003 - Dec 2008

Director - New Leads Chemistry

Lawrence Township, Nj, Us

- Managed three Hits to Leads chemistry groups totaling ~25 chemists that concurrently collaborated with ~10 ongoing early phase and full phase medicinal chemistry teams to prepare program analogs using a variety of automated solid phase, solution phase, or mixed solution/solid phase methodologies.- Directed a group of three computational chemists dedicated to developing database and computational methodology to support array synthesis and combinatorial chemistry. Oversaw the development of proprietary computational tools to triage hits from high throughput screening.- Served as the Chemistry Project Manager for the BMS/3DP ThermoFluor collaboration. Directed the screening and chemistry efforts of ~20 FTEs that prepared novel analogs for newly identified genomics targets.- Directed a biotransformation group of three scientists that prepared synthesis intermediates and metabolites using enzymatic processes.- Established the Fast Analog Synthesis Team (FAST), a group of synthetic chemists dedicated to the synthesis of arrays of focused program analogs.

Jul 2001 - Dec 2002

Associate Director - Combinatorial Drug Discovery

Lawrence Township, Nj, Us

- Managed an integrated team consisting of four different groups working on large library synthesis, Hits to Leads chemistry, and computational design- Directed a large library synthesis group of eight chemists that designed and synthesized diverse and drug-like combinatorial libraries to enhance the compound screening collection. In collaboration with the high throughput screening group, advanced multiple successful focused screening campaigns utilizing target class directed combinatorial libraries- Directed two Hits to Leads chemistry groups totaling ~20 chemists that concurrently collaborated with ~10 ongoing full phase and early phase medicinal chemistry programs to advance SAR using a variety of automated solid phase, solution phase, or mixed solution/solid phase methodologies- Directed a group of three computational chemists dedicated to developing databases and computational methodology to support array synthesis and combinatorial chemistry. The team developed a proprietary combinatorial informatics system that was exchanged for genomics technology from Exelixis. Additional projects included the development of computational tools to virtually screen trillions of potential combinatorial compounds, computational tools to design multi-component combinatorial libraries optimized using genetic algorithms, and an interactive program to efficiently display and analyze HTS screening data- Initiated and co-supervised the BMS/IRORI NanoKan collaboration that led to the successful development and implementation of an automated synthesis system capable of the efficient preparation of 10-20K combinatorial libraries- Served as the Chemistry Project Manager for the BMS/3DP ThermoFluor collaboration. Directed the screening and chemistry efforts of ~20 FTEs that prepared novel analogs for newly identified genomics based anti-infective targets- Served as the Kinase Target Team co-chair. Organized focused screening efforts and assemblage of 10K kinase mini decks

Jul 1998 - Jun 2001

Senior Principal Scientist - Combinatorial Drug Discovery

Lawrence Township, Nj, Us

Jul 1997 - Jun 1998

Research Group Leader - Combinatorial Drug Discovery

Lawrence Township, Nj, Us

- Supervised a combinatorial chemistry synthesis group of 16 chemists which concurrently collaborated with multiple ongoing full phase and early phase programs to prepare new analogs using a variety of automated solid phase, solution phase, or mixed solution/solid phase methodologies.- Identified three development candidates using combinatorial and automated array synthesis methodology, including lomitapide, a novel inhibitor of microsomal triglyceride transfer protein (MTP). Lomitapide was the first BMS clinical candidate to be prepared initially via robotics.- Advanced the development of novel solid phase chemistry methodology and linker technology.- Authored an ISIS based multi-form interface for use by ~1,200 scientists which provided the first integrated enterprise-wide informatics tool at BMS that combined chemical, biological, and high throughput screening data from different corporate Oracle databases.- Authored an ISIS based multi-form interface which integrated commercial reagent data, in-house reagent inventory, combinatorial synthesis reagent data, and combinatorial synthesis product data from commercial ISIS databases and corporate Oracle databases.- Authored an Excel based Synthesis Workbook for data handling during parallel and combinatorial synthesis which electronically integrated chemical synthesis information between corporate databases, local databases, Zymark robots, liquid handlers, mass specs, and HPLCs.- Authored an Excel based Ordering Workbook for automated purchasing of chemical reagents and laboratory supplies which provided a paperless path to secure needed materials.- Authored several Excel based Workbooks for automated data capture, data reduction, and database entry of biological assay results.

Jan 1995 - Jun 1997

Research Group Leader - Discovery Chemistry

Lawrence Township, Nj, Us

- Developed new methodology for the synthesis of phosphonate diester prodrugs.- Developed novel phosphonate pro-drug analogs of squalene synthase inhibitors.

Jul 1993 - Dec 1994

Research Group Leader - Chemical Process Research

Lawrence Township, Nj, Us

- Developed improved chemical syntheses of lead drug candidates.- Developed an improved production scale synthesis of the anti-thrombotic agent ifetroban which reduced the length of the route from 16 steps to 7 steps.- Developed a novel production scale semi-synthesis of the anticancer agent paclitaxel from 10-desacetylbaccatin III.

Jan 1992 - Jun 1993

Senior Research Investigator I - Discovery Chemistry

Lawrence Township, Nj, Us

- Designed and synthesized angiotensin II receptor antagonists.- Identified and developed four different lead series.- Lead compound approved as a development candidate, advanced to investigational toxicology.- Developed new methodology for the synthesis of tetrazoles.

Jul 1990 - Dec 1991

Research Investigator - Discovery Chemistry

Lawrence Township, Nj, Us

- Designed and synthesized inhibitors of the aspartyl protease, renin.- Developed a novel sulfonamide protecting group.- Developed new methodology for the synthesis of amidines and guanidines.- Developed new methodology for the preparation of imidazolones.

Jun 1986 - Jun 1990

Senior Research Chemist - Molecular Modeling

Rahway, New Jersey, Us

- Modeled biologically active compounds interacting with proteins and enzymes.- Developed software applicable to the solution of medicinal chemistry problems.- Designed and synthesized potential therapeutic agents for the treatment of hypercholesterolemia.

Dec 1985 - May 1986

Computer Software Consultant

Rochester, New York, Us

- Authored new code to better integrate in house hardware and software.

Jan 1982 - Nov 1985
2 education records

Michael Poss education

Doctor Of Philosophy - Phd, Organic Chemistry

University Of Rochester

Bachelor Of Science - Bs, Chemistry

University Of Rochester
FAQ

Frequently asked questions about Michael Poss

Quick answers generated from the profile data available on this page.

What company does Michael Poss work for?

Michael Poss works for Syneron Bio.

What is Michael Poss's role at Syneron Bio?

Michael Poss is listed as Senior Vice President, Peptide Chemistry at Syneron Bio.

What is Michael Poss's email address?

AeroLeads has found 1 work email signal at @bms.com for Michael Poss at Syneron Bio.

Where is Michael Poss based?

Michael Poss is based in Trenton, New Jersey, United States while working with Syneron Bio.

What companies has Michael Poss worked for?

Michael Poss has worked for Syneron Bio, Syneron Tech, Bristol Myers Squibb, Merck, and Eastman Kodak Company.

How can I contact Michael Poss?

You can use AeroLeads to view verified contact signals for Michael Poss at Syneron Bio, including work email, phone, and LinkedIn data when available.

What schools did Michael Poss attend?

Michael Poss holds Doctor Of Philosophy - Phd, Organic Chemistry from University Of Rochester.

What skills is Michael Poss known for?

Michael Poss is listed with skills including Pharmaceutical Industry, Drug Discovery, Drug Development, Clinical Development, Technology Transfer, Life Sciences, Organic Chemistry, and Oncology.

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