This role sits at the intersection of data engineering, data science, and drug development. You ... You will also manage vendor relationships and data procurement, evaluating and integrating new data ...
This role sits at the intersection of data engineering, data science, and drug development. You ... You will also manage vendor relationships and data procurement, evaluating and integrating new data ...
Associate Director, Development
College Park, MD · On-site
$106K - $127K/yr
The Associate Director of Development will manage a portfolio of approximately 80 major gift prospects with the objective of discovering, qualifying, cultivating, soliciting, closing, and stewarding ...
Associate Director, Development
College Park, MD · On-site
$106K - $127K/yr
The Associate Director of Development will manage a portfolio of approximately 80 major gift prospects with the objective of discovering, qualifying, cultivating, soliciting, closing, and stewarding ...
Associate Director, Chemical Development
Irvine, CA · On-site +1
... related to drug substance development and manufacturing at CMOs from preclinical through ... Manage API operations across assigned CMC programs and ensure operational plans align with ...
Associate Director, Chemical Development
Irvine, CA · On-site +1
... related to drug substance development and manufacturing at CMOs from preclinical through ... Manage API operations across assigned CMC programs and ensure operational plans align with ...
Reporting to the Sr Director of Pharmaceutical Development, the Associate Director of ... Manage day-to-day clinical drug product manufacturing activities at CDMOs to ensure timely delivery.
Quick apply
Reporting to the Sr Director of Pharmaceutical Development, the Associate Director of ... Manage day-to-day clinical drug product manufacturing activities at CDMOs to ensure timely delivery.
Director, Drug Substance
Redwood City, CA · On-site
$211K - $264K/yr
Playing a critical role as a technical lead within the Drug Substance function, the position will ... development. * Strong people management skills. * Hands-on proficiency in synthetic organic ...
Director, Drug Substance
Redwood City, CA · On-site
$211K - $264K/yr
Playing a critical role as a technical lead within the Drug Substance function, the position will ... development. * Strong people management skills. * Hands-on proficiency in synthetic organic ...
Lead & advance talent-- from manager to associate-director ready talent-- with emphasis on ... end drug development process and a proven ability to deliver results. * Have excellent written ...
New
Lead & advance talent-- from manager to associate-director ready talent-- with emphasis on ... end drug development process and a proven ability to deliver results. * Have excellent written ...
New
Lead & advance talent-- from manager to associate-director ready talent-- with emphasis on ... end drug development process and a proven ability to deliver results * Have excellent written ...
Lead & advance talent-- from manager to associate-director ready talent-- with emphasis on ... end drug development process and a proven ability to deliver results * Have excellent written ...
Associate Director, Biostatistics
Cambridge, MA · On-site
$218K - $264K/yr
Manages multiple studies to ensure consistency and adherence to standards within an indication or ... the drug development process * Compliant with BMS processes and SOPs, adherence to global and ...
Associate Director, Biostatistics
Cambridge, MA · On-site
$218K - $264K/yr
Manages multiple studies to ensure consistency and adherence to standards within an indication or ... the drug development process * Compliant with BMS processes and SOPs, adherence to global and ...
... GSK's drug development portfolio. Working under the direction of the Core Portfolio Lead, the ... The Associate Director contributes to integrated evidence plans across a range of development ...
... GSK's drug development portfolio. Working under the direction of the Core Portfolio Lead, the ... The Associate Director contributes to integrated evidence plans across a range of development ...
Sr. Manager/Associate Director, Clinical Pharmacology
Princeton, NJ · On-site
$150K - $200K/yr
Weare seeking a high-quality Senior Manager/Associate Director of Clinical Pharmacology to lead the ... Perform pharmacometric analyses to support drug development and address scientific questions.
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Sr. Manager/Associate Director, Clinical Pharmacology
Princeton, NJ · On-site
$150K - $200K/yr
Weare seeking a high-quality Senior Manager/Associate Director of Clinical Pharmacology to lead the ... Perform pharmacometric analyses to support drug development and address scientific questions.
Associate Director, Biostatistics
Somerset, NJ · On-site +1
$145K - $160K/yr
Strong understanding of the drug development process and applicable regulatory requirements ... risk management, quality oversight, and team development. * Excellent communication and ...
Associate Director, Biostatistics
Somerset, NJ · On-site +1
$145K - $160K/yr
Strong understanding of the drug development process and applicable regulatory requirements ... risk management, quality oversight, and team development. * Excellent communication and ...
Manage a portfolio of 100+ households to build meaningful relationships and solicit leadership ... The associate director of museum development will have direct contact with museum staff and key ...
New
Manage a portfolio of 100+ households to build meaningful relationships and solicit leadership ... The associate director of museum development will have direct contact with museum staff and key ...
New
... Director of the Sealy Institute for Drug Discovery ("SIDD"), the Associate Director, Assay ... Manage assay development projects, including timelines, resources, and budget allocation.
... Director of the Sealy Institute for Drug Discovery ("SIDD"), the Associate Director, Assay ... Manage assay development projects, including timelines, resources, and budget allocation.
Sr. Program Manager, Drug Development
San Diego, CA · On-site
$123K - $123K/yr
Lead drug development teams in partnership with the Program Lead, to develop cross-functional ... Serve as a Program Management expert resource for the broader organization * Contribute to the ...
Sr. Program Manager, Drug Development
San Diego, CA · On-site
$123K - $123K/yr
Lead drug development teams in partnership with the Program Lead, to develop cross-functional ... Serve as a Program Management expert resource for the broader organization * Contribute to the ...
The Director, Drug Safety & Pharmacovigilance Scientist provides strategic and scientific ... risk management activities across Dyne's development programs. This role characterizes and ...
The Director, Drug Safety & Pharmacovigilance Scientist provides strategic and scientific ... risk management activities across Dyne's development programs. This role characterizes and ...
Associate Director of Development
Colorado Springs, CO · Hybrid
$65K - $76K/yr
Plus, benefit from affordable dental, vision plans, and competitive prescription drug prices ... Identify, attract and manage prospective donors, and manage/retain assigned existing donors ...
Associate Director of Development
Colorado Springs, CO · Hybrid
$65K - $76K/yr
Plus, benefit from affordable dental, vision plans, and competitive prescription drug prices ... Identify, attract and manage prospective donors, and manage/retain assigned existing donors ...
Our client is seeking an Associate Director of Development to lead and manage projects from inception through completion while providing mentorship and support to development staff. Additionally, the ...
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Our client is seeking an Associate Director of Development to lead and manage projects from inception through completion while providing mentorship and support to development staff. Additionally, the ...
Associate Director, Clinical Development Trial Lead (CDTL)
Stamford, CT · On-site
$104.63/hr
Demonstrate independent leadership and influence when working with study teams, management, and ... Leverage and demonstrate broad understanding of therapeutic, clinical drug development, and process ...
Associate Director, Clinical Development Trial Lead (CDTL)
Stamford, CT · On-site
$104.63/hr
Demonstrate independent leadership and influence when working with study teams, management, and ... Leverage and demonstrate broad understanding of therapeutic, clinical drug development, and process ...
Centessa is seeking a (Associate) Director, Program Management - Orexin Development Programs ... This individual will leverage both project management and drug development experience to manage one ...
Centessa is seeking a (Associate) Director, Program Management - Orexin Development Programs ... This individual will leverage both project management and drug development experience to manage one ...
Lead the design, optimization, and execution of process development for PMO and ASO payload ... conjugated drug substances. * Innovate & Improve: Proactively identify and implement emerging ...
Lead the design, optimization, and execution of process development for PMO and ASO payload ... conjugated drug substances. * Innovate & Improve: Proactively identify and implement emerging ...
Associate Director Drug Development Management information
See salary details
$21K - $35.5K
1% of jobs
$35.5K - $49.9K
3% of jobs
$49.9K - $64.4K
12% of jobs
$71.2K is the 25th percentile. Wages below this are outliers.
$64.4K - $78.8K
19% of jobs
The median wage is $85K / yr.
$78.8K - $93.3K
35% of jobs
$98.7K is the 75th percentile. Wages above this are outliers.
$93.3K - $107.7K
13% of jobs
$107.7K - $122.2K
6% of jobs
$122.2K - $136.6K
4% of jobs
$136.6K - $151.1K
3% of jobs
$151.1K - $165.5K
1% of jobs
$165.5K - $180K
2% of jobs
$21K
$93.3K
$180K
How much do associate director drug development management jobs pay per year?
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For Associate Director Drug Development Management jobs, the most frequently searched job titles are:
Associate Director/Director, Data Science (Real World Data)
Boston, MA • On-site
Full-time
Re-posted 13 days ago
Job description
Formation Bio is a tech and AI driven pharma company differentiated by radically more efficient drug development.
Advancements in AI and drug discovery are creating more candidate drugs than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of new medicines that can reach patients, Formation Bio, founded in 2016 as TrialSpark Inc., has built technology platforms, processes, and capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses drugs from pharma companies, research organizations, and biotechs to develop programs past clinical proof of concept and beyond, ultimately helping to bring new medicines to patients. The company is backed by investors across pharma and tech, including a16z, Sequoia, Sanofi, Thrive Capital, John Doerr, Spark Capital, SV Angel Growth, and others.
You can read more at the following links:
- Our Vision for AI in Pharma
- Our Current Drug Portfolio
- Our Technology & Platform
At Formation Bio, our values are the driving force behind our mission to revolutionize the pharma industry. Every team and individual at the company shares these same values, and every team and individual plays a key part in our mission to bring new treatments to patients faster and more efficiently.
About the Position
As Associate Director of RWD Intelligence at Formation Bio, you will lead the strategy and execution of our real-world data (RWD) capabilities, building the data foundations that power drug acquisition, clinical development, and portfolio decision-making. You will own the end-to-end lifecycle of RWD: sourcing, procurement, ingestion, harmonization, quality assurance, and delivery of analysis-ready datasets to downstream consumers across Product, Data Science, Clinical Development, and Business Development.
This role sits at the intersection of data engineering, data science, and drug development. You will build and maintain scalable data infrastructure (pipelines, data models, lakes/marts) while ensuring semantic interoperability across heterogeneous data sources through ontology-driven harmonization frameworks such as OMOP. You will also manage vendor relationships and data procurement, evaluating and integrating new data assets as the portfolio evolves. The ideal candidate combines deep RWD domain expertise with strong data fluency, enabling Formation Bio to treat real-world evidence as a first-class strategic asset.
Responsibilities
- Lead the RWD Intelligence function within Data Science, owning data strategy, sourcing, and delivery of analysis-ready datasets
- Architect and maintain the supporting infrastructure (pipelines, ingestion workflows, data models, lakes/marts) across EHR/EMR, claims, registries, and genomics-linked cohorts
- Drive adoption and extension of harmonization frameworks (e.g., OMOP CDM) across heterogeneous data sources, leveraging AI/ML tools for entity resolution, ontology mapping, data quality monitoring, and automated harmonization
- Manage RWD vendor relationships end-to-end: evaluate providers, negotiate data use agreements, broker new partnerships, and integrate acquired datasets into the platform
- Partner with Data Science, Clinical Development, Business Development, and Engineering teams to define RWD use cases (trial feasibility, synthetic control arms, epidemiology, label expansion) and productize ad hoc pipelines into scalable, production-grade systems
- Foster a culture of data quality rigor, documentation, and reproducibility across all RWD assets
About You
Required Qualifications
- BSc or MSc in biomedical informatics, computational sciences, epidemiology, or a related quantitative field
- 5+ years of industry experience working directly with real-world data (EHR/EMR, claims, registries, linked biobank data) in pharma, biotech, health tech, or consulting, with at least 2+ years in people management
- Strong data engineering proficiency (pipelines, ingestion frameworks, data models, data lakes/marts) combined with deep working knowledge of biological and medical ontologies (ICD, SNOMED CT, MedDRA, RxNorm, ATC) and harmonization standards, particularly OMOP CDM
- Demonstrated experience with RWD procurement and vendor management: evaluating data providers, negotiating agreements, and integrating new data assets
- Proven ability to deliver RWD-derived insights across multiple drug development use cases (e.g., trial design, epidemiology, comparative effectiveness, label expansion), with familiarity across the development lifecycle from target selection through post-market
- Proficiency with modern AI/ML tools, including large language models, and their applications in data engineering and harmonization workflows
- Strong communication skills with the ability to translate complex data infrastructure concepts for clinical, scientific, and executive audiences
Preferred Qualifications
- PhD in biomedical informatics, epidemiology, computational biology, or a related field
- Experience with large-scale biobank and genomics-linked RWD platforms (UK Biobank, FinnGen, All of Us), with a track record of building RWD infrastructure that directly influenced drug acquisition, licensing, or portfolio decisions
- Familiarity with additional biomedical data modalities (scientific literature mining, -omics datasets, molecular data integration) and with data science/analytics methodologies applied to RWD (causal inference, trial simulation, propensity score methods)
- Background transitioning data infrastructure from research/ad hoc to production-grade systems in regulated environments
- Experience working at the intersection of data engineering, data science, and business strategy in pharma/biotech
Total Compensation Range:$213,500 - $267,000
Compensation Individual compensation is determined by several factors, including role scope, geographic location, and skills & experience. Your offer will reflect where you fall within the range based on these considerations. In addition to base salary, we offer equity, comprehensive benefits, and generous perks. If the posted range doesn't match your expectations, we still encourage you to apply!
Where We Hire Formation Bio is prioritizing hiring in key hubs, primarily the New York City and Boston metro areas, with a hybrid model requiring 3 days per week in office. Applicants from the Research Triangle (NC) and San Francisco Bay Area may also be considered. Please apply only if you reside in these locations or are willing to relocate
Equal Opportunity Formation Bio is committed to building a diverse and inclusive team. We are an equal opportunity employer and welcome candidates from all backgrounds. All qualified applicants will receive consideration for employment without regard to race, color, creed, religion, national origin, ancestry, sex (including pregnancy, childbirth, breastfeeding, and related medical conditions), gender identity or expression, sexual orientation, age, disability, genetic information, marital status, military or veteran status, or any other characteristic protected by federal, state, or local law.
About Formation Bio
Sourced by ZipRecruiter
Industry
Biotechnology research and development
Company size
51 - 200 Employees
Headquarters location
New York, NY, US
Year founded
2014