Boehringer Ingelheim
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AD, Pharmacometrics
role at
Boehringer Ingelheim .
3 days ago – Be among the first 25 applicants.
Description As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the company’s success. We realize that our strength and competitive advantage lie with our people. We support our employees in several ways to foster a healthy working environment, meaningful work, mobility, networking, and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim’s high regard for our employees.
Duties & Responsibilities
Develop PMx strategy and contribute to the clinical development plan and implement model-informed drug discovery and development (MID3) in clinical development projects with support of supervisor
Ensure timely delivery of state‑of‑the‑art PMx analyses for internal decision‑making throughout clinical drug development and registration with support of supervisor (e.g., non‑linear mixed‑effects models, model‑based meta‑analyses for dose selection, labeling, optimizing clinical study designs and pediatric development)
Ensure timely delivery of PMx internal documents with support of supervisor (e.g., dataset specification, PMx analysis plan, and PMx report)
Ensure timely delivery of documents where PMx is co‑author with support of supervisor (e.g., clinical development plan, pediatric investigational plan, submission documents)
Represent PMx in clinical development teams and in initiatives and working groups with support of supervisor (e.g., process harmonization)
Organize and manage projects with external organizations with support of supervisor (e.g., academic institutions or CROs)
Continuously contribute to improving the PMx IT infrastructure (e.g., specific code libraries)
Understand current national and international regulations, local requirements, BI policies, and procedures as relevant to areas of expertise
Apply this knowledge to ensure safe and compliant practices, manage risks, and maximize opportunities for projects to succeed
Assume responsibility for direct reports as needed including recruiting and managing; mentor and develop scientific staff; direct and oversee analyses and results of junior level scientists
Requirements
Master’s Degree in Medicine, Pharmacometrics, Clinical Pharmacology, Pharmacy, Mathematics, Biology, Statistics, or equivalent area of focus with a minimum of four (4) years relevant experience in Pharmacometrics in the pharmaceutical industry, regulatory agencies, or academia
OR PhD in Medicine, Pharmacometrics, Clinical Pharmacology, Pharmacy, Mathematics, Biology, Statistics, or equivalent area of focus with a minimum of two (2) years relevant experience in Pharmacometrics in the pharmaceutical industry, regulatory agencies, or academia
OR Professional degree in pharmacy or medicine (e.g., PharmD, MD, Apotheker, Arzt) with a minimum of three (3) years relevant experience in Pharmacometrics in the pharmaceutical industry, regulatory agencies, or academia
Proficiency in applying PMx software (e.g., NONMEM, Monolix, R, SAS, PBPK software)
Basic knowledge in clinical pharmacology, clinical drug development, MID3, and regulatory guidelines
Compensation This position, AD, Pharmacometrics, offers a base salary typically between $140,000.00 and $222,000.00. The position may be eligible for a role‑specific variable or performance‑based bonus and other compensation elements. For an overview of our benefits, please see the company's benefits page.
Eligibility Requirements
Must be legally authorized to work in the United States without restriction
Must be willing to take a drug test and post‑offer physical (if required)
Must be 18 years of age or older
Seniority level Mid‑Senior level
Employment type Full‑time
Job function Other
Industries Pharmaceutical Manufacturing
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AD, Pharmacometrics
role at
Boehringer Ingelheim .
3 days ago – Be among the first 25 applicants.
Description As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the company’s success. We realize that our strength and competitive advantage lie with our people. We support our employees in several ways to foster a healthy working environment, meaningful work, mobility, networking, and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim’s high regard for our employees.
Duties & Responsibilities
Develop PMx strategy and contribute to the clinical development plan and implement model-informed drug discovery and development (MID3) in clinical development projects with support of supervisor
Ensure timely delivery of state‑of‑the‑art PMx analyses for internal decision‑making throughout clinical drug development and registration with support of supervisor (e.g., non‑linear mixed‑effects models, model‑based meta‑analyses for dose selection, labeling, optimizing clinical study designs and pediatric development)
Ensure timely delivery of PMx internal documents with support of supervisor (e.g., dataset specification, PMx analysis plan, and PMx report)
Ensure timely delivery of documents where PMx is co‑author with support of supervisor (e.g., clinical development plan, pediatric investigational plan, submission documents)
Represent PMx in clinical development teams and in initiatives and working groups with support of supervisor (e.g., process harmonization)
Organize and manage projects with external organizations with support of supervisor (e.g., academic institutions or CROs)
Continuously contribute to improving the PMx IT infrastructure (e.g., specific code libraries)
Understand current national and international regulations, local requirements, BI policies, and procedures as relevant to areas of expertise
Apply this knowledge to ensure safe and compliant practices, manage risks, and maximize opportunities for projects to succeed
Assume responsibility for direct reports as needed including recruiting and managing; mentor and develop scientific staff; direct and oversee analyses and results of junior level scientists
Requirements
Master’s Degree in Medicine, Pharmacometrics, Clinical Pharmacology, Pharmacy, Mathematics, Biology, Statistics, or equivalent area of focus with a minimum of four (4) years relevant experience in Pharmacometrics in the pharmaceutical industry, regulatory agencies, or academia
OR PhD in Medicine, Pharmacometrics, Clinical Pharmacology, Pharmacy, Mathematics, Biology, Statistics, or equivalent area of focus with a minimum of two (2) years relevant experience in Pharmacometrics in the pharmaceutical industry, regulatory agencies, or academia
OR Professional degree in pharmacy or medicine (e.g., PharmD, MD, Apotheker, Arzt) with a minimum of three (3) years relevant experience in Pharmacometrics in the pharmaceutical industry, regulatory agencies, or academia
Proficiency in applying PMx software (e.g., NONMEM, Monolix, R, SAS, PBPK software)
Basic knowledge in clinical pharmacology, clinical drug development, MID3, and regulatory guidelines
Compensation This position, AD, Pharmacometrics, offers a base salary typically between $140,000.00 and $222,000.00. The position may be eligible for a role‑specific variable or performance‑based bonus and other compensation elements. For an overview of our benefits, please see the company's benefits page.
Eligibility Requirements
Must be legally authorized to work in the United States without restriction
Must be willing to take a drug test and post‑offer physical (if required)
Must be 18 years of age or older
Seniority level Mid‑Senior level
Employment type Full‑time
Job function Other
Industries Pharmaceutical Manufacturing
#J-18808-Ljbffr