The Director, Resource Management (DRM) is a key liaison across multiple functions in Research and Preclinical Development (RpD) providing comprehensive resource management and strategic resource ...
The Director, Resource Management (DRM) is a key liaison across multiple functions in Research and Preclinical Development (RpD) providing comprehensive resource management and strategic resource ...
Profluent is seeking a rigorous and highly collaborative Associate Director - Director to lead in ... pharmacology and preclinical development * Demonstrated experience designing, managing, and ...
Profluent is seeking a rigorous and highly collaborative Associate Director - Director to lead in ... pharmacology and preclinical development * Demonstrated experience designing, managing, and ...
Executive Director Preclinical Pharmacokinetics/Pharmacodynamics
Tarrytown, NY · Hybrid
$285K - $475K/yr
Build Our Future Together The Executive Director, Translational Pharmacokinetics and ... Contributes to the development of functional strategy. * Influential across the organization to ...
New
Executive Director Preclinical Pharmacokinetics/Pharmacodynamics
Tarrytown, NY · Hybrid
$285K - $475K/yr
Build Our Future Together The Executive Director, Translational Pharmacokinetics and ... Contributes to the development of functional strategy. * Influential across the organization to ...
New
Project Management & Strategic Operations Associate Director
Boston, MA · On-site
$155K - $233K/yr
The Associate Director, Preclinical Sciences, Program Management and Strategic Operations, will be ... development (full life-cycle)across multiple preclinical disciplines (e.g., research, drug ...
Project Management & Strategic Operations Associate Director
Boston, MA · On-site
$155K - $233K/yr
The Associate Director, Preclinical Sciences, Program Management and Strategic Operations, will be ... development (full life-cycle)across multiple preclinical disciplines (e.g., research, drug ...
Manager, Director, or Senior Director, Business Development: Preclinical Services
Atlanta, GA · On-site
$138K - $198K/yr
... development, preclinical and clinical research, regulatory affairs, and market access and ... At the Director level, you must have a Bachelor's Degree plus a minimum of 8+ years of demonstrated ...
Manager, Director, or Senior Director, Business Development: Preclinical Services
Atlanta, GA · On-site
$138K - $198K/yr
... development, preclinical and clinical research, regulatory affairs, and market access and ... At the Director level, you must have a Bachelor's Degree plus a minimum of 8+ years of demonstrated ...
Director, Clinical Development
Lexington, MA · On-site
$89K - $122K/yr
... preclinical programs utilizing our versatile RNA medicines platform. Driven by the calling to ... The Director, Clinical Development will collaborate closely with cross-functional partners ...
Director, Clinical Development
Lexington, MA · On-site
$89K - $122K/yr
... preclinical programs utilizing our versatile RNA medicines platform. Driven by the calling to ... The Director, Clinical Development will collaborate closely with cross-functional partners ...
Director, Clinical Development
$89K - $122K/yr
... preclinical programs utilizing our versatile RNA medicines platform. Driven by the calling to ... The Director, Clinical Development will collaborate closely with cross-functional partners ...
Director, Clinical Development
$89K - $122K/yr
... preclinical programs utilizing our versatile RNA medicines platform. Driven by the calling to ... The Director, Clinical Development will collaborate closely with cross-functional partners ...
Director, Discovery Process Chemistry, West Point, PA Throughout the drug discovery lifecycle ... development, and support of API campaigns for discovery and preclinical efforts; transferring ...
Director, Discovery Process Chemistry, West Point, PA Throughout the drug discovery lifecycle ... development, and support of API campaigns for discovery and preclinical efforts; transferring ...
Plan, direct, coordinate, and execute activities related to the design, initiation. and follow-up ... Oversee the development of and modifications to preclinical models to address project needs.
Plan, direct, coordinate, and execute activities related to the design, initiation. and follow-up ... Oversee the development of and modifications to preclinical models to address project needs.
... through preclinical development, enabling robust, scalable, and translatable delivery solutions ... The Sr Director will operate at the intersection of Platform, Programs and Technical Development ...
... through preclinical development, enabling robust, scalable, and translatable delivery solutions ... The Sr Director will operate at the intersection of Platform, Programs and Technical Development ...
Project Management & Strategic Operations Associate Director
Boston, MA · Hybrid
$155K - $233K/yr
The Associate Director, Preclinical Sciences, Program Management and Strategic Operations, will be ... development (full life-cycle)across multiple preclinical disciplines (e.g., research, drug ...
Project Management & Strategic Operations Associate Director
Boston, MA · Hybrid
$155K - $233K/yr
The Associate Director, Preclinical Sciences, Program Management and Strategic Operations, will be ... development (full life-cycle)across multiple preclinical disciplines (e.g., research, drug ...
Profluent is seeking a rigorous and highly collaborative Associate Director - Director to lead in ... pharmacology and preclinical development * Demonstrated experience designing, managing, and ...
Profluent is seeking a rigorous and highly collaborative Associate Director - Director to lead in ... pharmacology and preclinical development * Demonstrated experience designing, managing, and ...
Plan, direct, coordinate, and execute activities related to the design, initiation. and follow-up ... Oversee the development of and modifications to preclinical models to address project needs.
Plan, direct, coordinate, and execute activities related to the design, initiation. and follow-up ... Oversee the development of and modifications to preclinical models to address project needs.
Senior Director, Delivery
Cambridge, MA · On-site
... through preclinical development, enabling robust, scalable, and translatable delivery solutions ... The Sr Director will operate at the intersection of Platform, Programs and Technical Development ...
Senior Director, Delivery
Cambridge, MA · On-site
... through preclinical development, enabling robust, scalable, and translatable delivery solutions ... The Sr Director will operate at the intersection of Platform, Programs and Technical Development ...
Director, Discovery Process Chemistry, West Point, PA Throughout the drug discovery lifecycle ... development, and support of API campaigns for discovery and preclinical efforts; transferring ...
Director, Discovery Process Chemistry, West Point, PA Throughout the drug discovery lifecycle ... development, and support of API campaigns for discovery and preclinical efforts; transferring ...
Senior Director, Quantitative Pharmacology Sun Pharma is the world's fourth largest specialty ... The incumbent will report into the Vice President of Preclinical Development and Translational ...
Senior Director, Quantitative Pharmacology Sun Pharma is the world's fourth largest specialty ... The incumbent will report into the Vice President of Preclinical Development and Translational ...
Plan, direct, coordinate, and execute activities related to the design, initiation. and follow-up ... Oversee the development of and modifications to preclinical models to address project needs.
Quick apply
Plan, direct, coordinate, and execute activities related to the design, initiation. and follow-up ... Oversee the development of and modifications to preclinical models to address project needs.
Pioneering Medicines is seeking an ambitious, innovative and highly collaborative leader (Director ... preclinical development. The ideal candidate will have recognized expertise in laboratory ...
Pioneering Medicines is seeking an ambitious, innovative and highly collaborative leader (Director ... preclinical development. The ideal candidate will have recognized expertise in laboratory ...
... preclinical development and translational planning. In this role, you will help advance internal ... Direct experience with translational endpoints such as pharmacodynamic biomarkers, disease-relevant ...
... preclinical development and translational planning. In this role, you will help advance internal ... Direct experience with translational endpoints such as pharmacodynamic biomarkers, disease-relevant ...
Reporting to the Chief Business Officer, the Director of Business Development works ... in preclinical development, as well as additional discovery candidates. The Company is based in ...
Reporting to the Chief Business Officer, the Director of Business Development works ... in preclinical development, as well as additional discovery candidates. The Company is based in ...
Director Preclinical Development information
See salary details
$40.5K - $50.9K
5% of jobs
$50.9K - $61.3K
9% of jobs
$69.1K is the 25th percentile. Wages below this are outliers.
$61.3K - $71.7K
15% of jobs
$71.7K - $82.1K
16% of jobs
The median wage is $85.6K / yr.
$82.1K - $92.5K
16% of jobs
$92.5K - $103K
14% of jobs
$103.5K is the 75th percentile. Wages above this are outliers.
$103K - $113.4K
10% of jobs
$113.4K - $123.8K
6% of jobs
$123.8K - $134.2K
4% of jobs
$134.2K - $144.6K
3% of jobs
$144.6K - $155K
2% of jobs
$40.5K
$92.4K
$155K
How much do director preclinical development jobs pay per year?
What is a Director Preclinical Development job?
A Director of Preclinical Development oversees the early-stage research and testing of drug candidates before they enter clinical trials. They manage preclinical studies, ensuring regulatory compliance, safety, and efficacy assessments. This role involves coordinating with cross-functional teams, external partners, and regulatory agencies to advance promising compounds. Strong expertise in toxicology, pharmacology, and regulatory guidelines is essential. The director plays a key role in shaping the preclinical strategy to support successful drug development.
What are the key skills and qualifications needed to thrive in the Director Preclinical Development position, and why are they important?
To thrive as a Director Preclinical Development, you need deep expertise in pharmaceutical or biotechnology research, strong project management abilities, and an advanced degree (Ph.D., Pharm.D., or equivalent) in a life sciences field. Familiarity with regulatory guidelines (such as GLP), experience using data management and statistical analysis software, and prior leadership roles in preclinical studies are essential. Exceptional communication, problem-solving, and team leadership skills set candidates apart in managing multidisciplinary teams and collaborative projects. These competencies are crucial for successfully guiding drug candidates through preclinical stages while ensuring regulatory compliance and timely project delivery.
What are the typical responsibilities and team dynamics for a Director of Preclinical Development?
A Director of Preclinical Development is responsible for overseeing the planning, execution, and management of preclinical research programs, ensuring that studies meet scientific, regulatory, and project milestones. You will typically work with cross-functional teams including toxicologists, pharmacologists, regulatory affairs professionals, and external partners, fostering collaboration throughout the drug development process. The role often involves reviewing study designs and data, preparing regulatory submissions, and providing strategic direction to advance compounds toward clinical testing. Working closely with upper management, you'll play a key part in shaping research priorities and resource allocation. This position offers significant influence over drug development strategies and opportunities for advancement to higher executive or scientific leadership roles.
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Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 5 days ago
Regeneron rating
8.7
Based on 42 frontline employees who took The Breakroom Quiz
13th of 71 rated pharmaceutical
Job description
The Director, Resource Management (DRM) is a key liaison across multiple functions in Research and Preclinical Development (RpD) providing comprehensive resource management and strategic resource planning for RpD functions with respect to current programs as well as planning for the future development portfolio. The DRM will supervise and coach two resource managers on the team. To be successful, the DRM will need to have an in-depth understanding of pharmaceutical discovery, pre-clinical development, research and early development functional roles, responsibilities and work effort. The DRM will be an expert in industry standard resource management tools and respective reporting tools to provide key insights regarding capacity, resource planning and forecasting. The DRM will be confident in the design of effective insight driven dashboards and collaborate closely with the IT function to enable development, implementation, and support. The DRM will promote the adherence to RM best practices, processes and the delivery of high-quality resource planning, capacity management, tracking, and forecasting of functional resources.
As a Director, a typical day may include the following:Serves as the key interface and point of contact with R&pD for the review and assessment of functional resource strategies including the assessment of available resources against requirements and confirmation of resource plans with functional leadership
Works with partners to ensure that Target, Project, and Program assumptions are current and resource utilization is optimized
Partners with applicable functions to design, develop, implement, and update algorithms in the RM tool used in resource demand forecasts
Directs other RMs assigned to additional functional areas to ensure cross-functional consistency for resource and headcount management
Assists partner functions with capacity management providing support for annual headcount planning and ensuring data quality for the quarterly budget reforecast activities
Deliver regular and ad-hoc resource reports, including forecasted resource demand, capacity, gap analyses, and FTE planned vs. actuals that provide clear insights needed for decision making
Is viewed as Subject Matter Expert (SME) in Resource Management for targets, assets, programs, and studies
Provides leadership and operational support for resource management processes including active resource management, capacity planning, and strategic workforce planning
Liaises with the Data Analytics (DA) team to design reports to help identify trends and develop metrics and analytics around resourcing and to develop functional and portfolio resourcing benchmarks and metrics
Conducts portfolio and program level scenario analyses. Models impact of changes in assumptions on resource estimates
Proactively identifies and communicates resource-related gaps, issues and risks to partner functions based on analysis of resource data. Supports review and discussion to resolve resource and/or capacity conflicts
Adept at managing a limited supply of resources against constantly changing portfolio
Excellent analytical, budgeting, and resource balancing skills
Problem solving abilities, troubleshooting, conflict resolution, and resourcefulness
Effective communication (clear and concise written and verbal skills), influencing, negotiating, and selling
Excellent interpersonal and leadership skills, ability to build relationships internally and externally (e.g. with supervisors, peers, partners and stakeholders)
Detail oriented and capable of working independently in ambiguous situations
Ability to manage multiple tasks and tight deadlines with confidence
Ability to prioritize and organize workload across multiple groups
Experience with supervising, coaching, and mentoring direct reports
Proficiency in Microsoft Office Suite
To be considered for this role, you must have a Bachelor's Degree required and 12+ years' experience in Biotech/Pharmaceutical/CRO, including, but not limited to, Research, Early and Late Development functional areas. Master's Degree (MS/MBA) and 10+ years of relevant experience may be considered. A solid understanding of the drug discovery and development process with particular emphasis on preclinical development, translational medicine, and early development for biological molecules. Expert with Planisware for project planning and resource forecasting including the design, development, and implementation of algorithms. We are seeking extensive experience with reporting for business facing resource management in research and development. This opportunity requires the ability to travel up to 20%.
Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.
Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.
Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed onsite. Please speak with your recruiter and hiring manager for more information about onsite expectations for your role and location.
As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.
For jobs in Canada: this posting is for an existing position.
Salary Range (annually)
$183,100.00 - $305,200.00What Regeneron employees say
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About Regeneron
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Industry
Biotechnology research and development
Company size
5,001 - 10,000 Employees
Headquarters location
Tarrytown, NY, US
Year founded
1988