Senior Toxicology Scientist & Study Director

MSD; Northern (KY); Hybride; USD 106 000 - 167 000; Plein temps

Avantages offerts par ce poste

Medical, dental, vision insurance

401(k) retirement plan

Paid holidays and vacation

Résumé du poste

Merck & Co., Inc. is seeking a Senior Scientist in Toxicology to conduct and monitor toxicity studies (GLP and non-GLP) as a Study Director or Study Monitor at the West Point, PA location.

The role leads in vivo study designs, integrates findings, and prepares reports for regulatory submissions. The candidate should hold a PhD in toxicology or related field and demonstrate strong leadership, cross-functional teamwork, and clear communication.

Qualifications

• PhD in toxicology, pharmacology, pharmaceutical sciences, or related scientific discipline.
• Strong interest in collaborating with cross-functional teams and communicating openly and often with colleagues.
• Ability to communicate clearly using verbal and written formats, including presentations.

Responsabilités

• Serve as the single point of control (Study Director) on assigned acute through chronic general toxicology studies across all modalities.
• Critically analyze and interpret data, integrate data from other areas (clinical pathology, pathology, toxicokinetics) in written reports for regulatory submissions.
• Ensure regulatory rigor, proactive risk identification, and timely study execution.
• Lead and/or participate in method development and inter-group initiatives as needed.

Connaissances

Animal Handling

CROs

Data Evaluation

Detail-Oriented

Experimentation

Exploratory Research

Good Laboratory Practices (GLPs)

In Vivo Models

Laboratory Research

Pre-Clinical Developments

Report Preparation

Situational Leadership

Study Directing

Study Monitoring

Timeline Management

Toxicological Risk Assessment

Toxicology

Formation

PhD in toxicology, pharmacology, pharmaceutical sciences, or related scientific discipline

Description du poste

Merck & Co., Inc. is seeking a Senior Scientist in Toxicology to conduct and monitor toxicity studies (GLP and non-GLP) as a Study Director or Study Monitor at the West Point, PA location.

The role leads in vivo study designs, integrates findings, and prepares reports for regulatory submissions. The candidate should hold a PhD in toxicology or related field and demonstrate strong leadership, cross-functional teamwork, and clear communication.