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Ronda Rippley

Senior Director, Head of Quantitative Pharmacology

Vice President, Head of Clinical Pharmacology at Constellation Pharmaceuticals

Cambridge, Massachusetts

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Ronda Rippley's Email Addresses & Phone Numbers

Ronda Rippley's Work Experience

Regeneron Pharmaceuticals, Inc.

Senior Director, Head of Quantitative Pharmacology

May 2017 to June 2019

Tarrytown, New York

Merck

Executive Director & Quantitative Pharmacology and Pharmacometrics Therapy Area Head [CMD, ID, WHE]

July 2016 to May 2017

Pennsylvania and New Jersey

Merck

Associate Director

September 2006 to December 2007

Ronda Rippley's Education

University of Houston

PhD, Chemical Engineering

1992 to 1996

University of Pennsylvania

MSE, Chemical and Biochemical Engineering

1990 to 1992

Montana State University-Bozeman

BS, Chemical Engineering

1986 to 1990

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About Ronda Rippley's Current Company

Regeneron Pharmaceuticals, Inc.

Frequently Asked Questions about Ronda Rippley

What company does Ronda Rippley work for?

Ronda Rippley works for Regeneron Pharmaceuticals, Inc.


What is Ronda Rippley's role at Regeneron Pharmaceuticals, Inc.?

Ronda Rippley is Senior Director, Head of Quantitative Pharmacology


What is Ronda Rippley's personal email address?

Ronda Rippley's personal email address is ro****[email protected]


What is Ronda Rippley's business email address?

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What is Ronda Rippley's Phone Number?

Ronda Rippley's phone (413) ***-*425


What industry does Ronda Rippley work in?

Ronda Rippley works in the Pharmaceuticals industry.


Who are Ronda Rippley's colleagues?

Ronda Rippley's colleagues are Ed Zhang, Constantine Chinoporos, Mark Woodruff, Xavier FACR, Jennifer Goodfellow, Shelley Knight, Philip Yin, and Alicia Clawson


About Ronda Rippley

📖 Summary

Senior Director, Head of Quantitative Pharmacology @ Regeneron Pharmaceuticals, Inc. From May 2017 to June 2019 (2 years 2 months) Tarrytown, New YorkExecutive Director & Quantitative Pharmacology and Pharmacometrics Therapy Area Head [CMD, ID, WHE] @ Merck From July 2016 to May 2017 (11 months) Pennsylvania and New JerseyAssociate Director @ Merck From September 2006 to December 2007 (1 year 4 months) Research Fellow/Senior Investigator @ Merck From September 2005 to September 2006 (1 year 1 month) Sr. Research Pharmacokineticist/Research Fellow @ Merck From December 1996 to June 2004 (7 years 7 months) Executive Director, Early Stage Quantitative Pharmacology & Pharmacometrics @ Merck Lead the Early Stage Quantitative Pharmacology and Pharmacometrics (QP2) group within the department of Pharmacokinetics, Pharmacodynamics and Drug Metabolism (PPDM), with business management and scientific oversight responsibilities for a staff of 20 scientists across 5 discovery and development sites. Accountable for developing and driving strategies to leverage quantitative pharmacology capabilities to increase confidence in target, molecule, and proof of concept through reduction of translational risk in the discovery and early development portfolio. Accountable for the collaborative design of clinical studies relating to the kinetics of drug absorption and disposition and for the evaluation (including PK/PD, physiological, comparator, and translational model-based approaches), interpretation, reporting, and integration of the resulting data in support of the ethical development and registration of human health drugs (small molecules, peptides, and large molecules). Responsible, in collaboration with QP2 leadership team, for global talent management (career development, performance management, retention) and resource allocation (internal as well as collaboration on external sourcing) to support core QP2 deliverables. Responsible for development of Early QP2 functional area strategic direction and organizational design to support growth and impact of the Early QP2 innovative core. Represent QP2 and PPDM on cross-functional teams and strategic initiatives. From November 2013 to June 2016 (2 years 8 months) West Point, PA and Kenilworth, NJDirector and Clinical PK/PD Site Lead @ Merck Lead Clinical PK/PD group in PA, with people management and scientific oversight responsibilities for 22 PhD-level scientists and associate scientists. Responsible, in collaboration with other functional leaders, for talent management (recruiting, career development, performance management, retention) and resource allocation (internal as well as collaboration on external sourcing) to support core Clinical PK/PD deliverables. Accountable, as part of senior leadership team, for collaborative design of clinical studies relating to the kinetics of drug absorption and disposition and for the evaluation (including PK/PD model-based approaches), interpretation, reporting, and integration of the resulting data in support of the ethical development of human health drugs. Represent PPDM (Pharmacokinetics, Pharmacodynamics, and Drug Metabolism) on several cross-functional teams and strategic initiatives, fulfilling a multidirectional business management role. From December 2007 to September 2011 (3 years 10 months) West Point, PAPrincipal Scientist @ Amgen Responsible for collaborating in the design and conduct of clinical and nonclinical studies (including discovery screening, IND-enabling PK, and GLP TK), relating to the kinetics of drug absorption and disposition and for the evaluation, interpretation, reporting, and integration of the resulting data in support of the ethical development of human therapeutics. Served as lead PK scientist on several cross-functional global development teams for a large-scale clinical development program involving a fully human monoclonal antibody under investigation for prevention of bone loss in osteoporosis, rheumatoid arthritis, and several oncology indications. Supervised a group of 6 employees. From July 2004 to August 2005 (1 year 2 months) Thousand Oaks, CAUS Lead, PK/PD @ Merck Lead Clinical PK/PD group in United States (PA, NJ), with business management and scientific/strategic oversight responsibilities for 35 PhD-level scientists and associate scientists. Responsible, in collaboration with other functional leaders, for talent management (recruiting, career development, performance management, retention) and resource allocation (internal as well as collaboration on external sourcing) to support core Clinical PK/PD deliverables. Accountable for developing appropriate business and organizational strategies to enable innovation and deliver effective performance of the business unit. Accountable, as part of senior leadership team, for driving human pharmacology strategy as well as collaborative design of clinical studies relating to the characterization of drug absorption, disposition, and effectiveness and for the evaluation (including PK/PD model-based approaches), interpretation, reporting, and integration of the resulting data in support of the ethical development and health authority registration of human health drugs. Responsible (as co-lead) for building capabilities and expanding application & impact of translational PK/PD methodologies throughout MRL Discovery pipeline. Represent PPDM (Pharmacokinetics, Pharmacodynamics, and Drug Metabolism) on several cross-functional teams and strategic initiatives, fulfilling a multidirectional business management and strategic role. From September 2011 to October 2013 (2 years 2 months) Vice President, Head of Clinical Pharmacology @ Constellation Pharmaceuticals Cambridge, Massachusetts, United StatesVice President, Clinical Pharmacology @ Boston Pharmaceuticals From June 2019 to August 2020 (1 year 3 months) Cambridge, Massachusetts


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Ronda Rippley's Personality Type

Extraversion (E), Intuition (N), Feeling (F), Judging (J)

Average Tenure

2 year(s), 5 month(s)

Ronda Rippley's Willingness to Change Jobs

Unlikely

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