Enanta Pharmaceuticals Jobs

Enanta Pharmaceuticals

Contract Research | Watertown, MA | 375 followers

Enanta Pharmaceuticals Overview

WEBSITE enanta.com
HEADQUARTERS Watertown, MA
SIZE 200 - 500
INDUSTRY Contract Research
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Head, Biometrics (Watertown, MA - Hybrid) at Enanta Pharmaceuticals

Watertown, MA | Full Time
$193k-252k (estimate)
2 Months Ago
Position Summary. Reporting to Enanta’s Chief Medical Officer, the Executive Director/Vice President, Biometrics will lead the biostatistics and statistical programming functions for Enanta’s rapidly expanding clinical portfolio of promising therapeutics in Infectious Disease and Inflammation.  In this position, you will play a key role in the strategy, development, and execution of the clinical pipeline.  With a strong technical, regulatory and ...

Manager, Contracts at Enanta Pharmaceuticals

Watertown, MA | Full Time
$124k-167k (estimate)
2 Months Ago
Position Summary. Enanta is seeking a bright, highly motivated, and thorough Contracts Manager experienced in preparing and negotiating contracts in healthcare R&D to join our team. In this role you will be responsible for the independent review and negotiation of a wide variety of contracts in support of Enanta’s drug discovery and development programs. You will report to the Associate Director, Contracts & Legal Counsel in the Legal Department ...

Head, Biometrics at Enanta Pharmaceuticals

Watertown, MA | Full Time
$189k-247k (estimate)
2 Months Ago
Position Summary. Reporting to Enanta’s Chief Medical Officer, the Executive Director/Vice President, Biometrics will lead the biostatistics and statistical programming functions for Enanta’s rapidly expanding clinical portfolio of promising therapeutics in Infectious Disease and Inflammation. In this position, you will play a key role in the strategy, development, and execution of the clinical pipeline. With a strong technical, regulatory and sc...

Manager, Contracts (Watertown, MA - Hybrid) at Enanta Pharmaceuticals

Watertown, MA | Full Time
$131k-174k (estimate)
2 Months Ago
Position Summary. Enanta is seeking a bright, highly motivated, and thorough Contracts Manager experienced in preparing and negotiating contracts in healthcare R&D to join our team. In this role you will be responsible for the independent review and negotiation of a wide variety of contracts in support of Enanta’s drug discovery and development programs. You will report to the Associate Director, Contracts & Legal Counsel in the Legal Department ...

Senior Director, Chemical Process Development & Manufacturing (Watertown, MA - Onsite) at Enanta Pharmaceuticals

Watertown, MA | Full Time
$182k-235k (estimate)
2 Months Ago
Job Summary. The Senior Director, Chemical Process Development and Manufacturing will design, execute, and lead chemical process development and manufacturing strategy to produce drug substances for GLP toxicology, clinical supplies and potential commercialization. This position will lead a group of chemists and serve as a technical expert in the area of drug substance throughout the organization and will coordinate/author/review drug substance r...

Associate Scientist, Drug Metabolism and Pharmacokinetics (DMPK) at Enanta Pharmaceuticals

Watertown, MA | Full Time
$135k-169k (estimate)
11 Months Ago
Job Summary. The Associate Scientist will work with an experienced Ph. D. scientist to conduct drug permeability and liver / intestine / lung / kidney transporter studies in support of Enanta drug discovery programs. She/he will be an integral member of Enanta’s highly collaborative Pharmacology and DMPK/Bioanalysis Department focused on the discovery of novel therapeutics against liver and viral diseases including nonalcoholic steatohepatitis (N...

Associate Director, Medical Writing at Enanta Pharmaceuticals

Watertown, MA | Full Time
$171k-212k (estimate)
0 Months Ago
Job Summary. The Medical Writer will lead medical writing activities for clinical documentation preparation to support the advancement of clinical-stage programs. Primary Responsibilities. Coordinate the preparation and timely delivery of high-quality documents for domestic and international regulatory filing and clinical programs. Produce documents to support clinical trials and regulatory submissions, in accordance with domestic and internation...
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