What are the responsibilities and job description for the Senior Quantitative Analyst position at Merck Sharp & Dohme (MSD)?
About Our Team: At Merck Sharp & Dohme (MSD), we are committed to fostering an inclusive and diverse workplace where talented individuals can thrive. As a member of our Quantitative Pharmacology team, you will have the opportunity to work on complex projects, collaborate with experts from diverse backgrounds, and contribute to the development of innovative tools and approaches.
We are seeking a highly skilled Associate Director of Pharmacometrics to lead our team. The successful candidate will have a Ph.D. or equivalent degree with at least 3 years of experience in pharmaceutical drug development or academia. They will possess expertise in performing pharmacometrics analyses, knowledge of drug development, pharmacokinetics, and pharmacology principles, and proficiency in standard pharmacometric software.
In this role, you will work closely with the QP2 department to apply pharmacometrics capabilities to optimize drug discovery and development programs. Your responsibilities will include developing and executing population pharmacokinetic models, PK/PD models, exposure response models, and disease progression modeling. You will also maintain a comprehensive understanding of global regulatory expectations for small molecules and biologics and author regulatory documents such as INDs, CSRs, and CTDs.
We are seeking a highly skilled Associate Director of Pharmacometrics to lead our team. The successful candidate will have a Ph.D. or equivalent degree with at least 3 years of experience in pharmaceutical drug development or academia. They will possess expertise in performing pharmacometrics analyses, knowledge of drug development, pharmacokinetics, and pharmacology principles, and proficiency in standard pharmacometric software.
In this role, you will work closely with the QP2 department to apply pharmacometrics capabilities to optimize drug discovery and development programs. Your responsibilities will include developing and executing population pharmacokinetic models, PK/PD models, exposure response models, and disease progression modeling. You will also maintain a comprehensive understanding of global regulatory expectations for small molecules and biologics and author regulatory documents such as INDs, CSRs, and CTDs.
