Sr. AD/ AD, Pharmacometrics (Remote)

Boehringer Ingelheim; Ridgefield (CT); Remote; USD 135,000 - 232,000; Full time

Job summary

An innovative pharmaceutical company is seeking a Senior Associate Director in Pharmacometrics to lead the development of model-informed drug discovery strategies. This role offers the opportunity to work in a dynamic environment that values diversity and innovation, contributing to the advancement of healthcare solutions. You will be responsible for managing projects, mentoring staff, and ensuring compliance with regulations while collaborating with international teams. Join a company that prioritizes employee well-being and professional growth, making a meaningful impact in the pharmaceutical industry.

Qualifications

• PhD or Master’s in relevant fields with specified years of experience.
• Proficiency in PMx software and knowledge of clinical pharmacology.

Responsibilities

• Develop PMx strategy and contribute to clinical development plans.
• Ensure timely delivery of PMx analyses for decision-making.

Skills

PMx software (NONMEM, Monolix, R, SAS, PBPK software)

Clinical pharmacology knowledge

Drug development knowledge

Regulatory guidelines knowledge

Education

PhD in relevant fields

Master’s in relevant fields

Job description

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Description

This is a multi-level posting. Candidates will be hired in at the level commensurate with their education, experience, and business need.

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 opportunities for all employees to collaborate internationally, offering visibility and the chance to directly contribute to the company's success. We support our employees through fostering a healthy working environment, meaningful work, mobility, networking, and work-life balance. Our competitive compensation and benefits reflect our high regard for our employees.

Responsibilities

• Develop PMx strategy and contribute to clinical development plans, implementing model-informed drug discovery and development (MID3).
• Ensure the timely delivery of PMx analyses and documents for decision-making and regulatory submissions.
• Represent PMx in project teams, authoring relevant documents and developing strategies.
• Manage projects with external organizations and contribute to improving PMx infrastructure.
• Understand and apply current regulations, policies, and procedures to ensure compliance and risk management.
• Mentor and develop scientific staff, overseeing analyses and results.

Requirements

Associate Director:

• PhD or Master’s in relevant fields with specified years of experience or equivalent professional degree with relevant industry experience.
• Proficiency in PMx software (e.g., NONMEM, Monolix, R, SAS, PBPK software).
• Basic knowledge of clinical pharmacology, drug development, MID3, and regulatory guidelines.

Senior Associate Director:

• Same qualifications as Associate Director but with more experience (minimum 4 years PhD or 6 years Master’s).
• Additional relevant experience in clinical development teams is preferred.
• Proficiency in PMx software and knowledge of clinical pharmacology and regulatory guidelines.

Compensation

Base salary typically ranges from $135,000 to $232,000, with potential bonuses and other compensation elements. For more benefits, visit our website.

Eligibility

• Legal authorization to work in the US without restrictions.
• Willingness to undergo drug testing and physicals if required.
• At least 18 years old.

Why Boehringer Ingelheim?

Develop your career in a culture that values diversity and innovation. We prioritize your development, health, and wellbeing, and are committed to making a positive impact through healthcare accessibility. Learn more at our website.

Additional Details

• Seniority level: Mid-Senior level
• Employment type: Full-time
• Job function: Other
• Industry: Pharmaceutical Manufacturing