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Reposted 11 Hours AgoSaved
In-Office
Boston, MA, USA
236K-354K Annually
Senior level
236K-354K Annually
Senior level
Biotech • Pharmaceutical
The Associate Director leads biostatistics efforts in clinical trials, manages team members, authors statistical plans, and collaborates cross-functionally while ensuring quality and compliance with regulatory standards.
Top Skills: RSAS
Reposted 11 Hours AgoSaved
In-Office
Boston, MA, USA
232K-348K Annually
Senior level
232K-348K Annually
Senior level
Biotech • Pharmaceutical
The Senior Director, Market Enablement will lead initiatives to enhance kidney product access, collaborate with various stakeholders, and drive market transformation efforts.
Reposted 11 Hours AgoSaved
In-Office
Boston, MA, USA
184K-276K Annually
Expert/Leader
184K-276K Annually
Expert/Leader
Biotech • Pharmaceutical
The Director of Master Data Management will lead the MDM strategy and operations, focusing on Customer, Supplier, and Product domains. Responsibilities include modernization of data systems, overseeing AI integration, and managing a high-performing team.
Top Skills: AIAWSDatabricksLarge Language ModelsMachine LearningMaster Data ManagementOracle ErpSalesforceSnowflakeVeeva
Reposted 11 Hours AgoSaved
In-Office
Boston, MA, USA
175K-263K Annually
Senior level
175K-263K Annually
Senior level
Biotech • Pharmaceutical
The Director leads the GxP training strategy, overseeing governance and compliance within the Quality Management System, while partnering with leadership for effective training solutions.
Top Skills: Learning Management System (Lms)Quality Management System (Qms)
Reposted 11 Hours AgoSaved
In-Office
Boston, MA, USA
158K-237K Annually
Senior level
158K-237K Annually
Senior level
Biotech • Pharmaceutical
The Associate Director will provide commercial insights through market research and analytics to inform strategic decisions in Vertex's biopharma products, particularly in kidney disease.
Top Skills: Biopharma CommercializationData AnalyticsMarket ResearchQuantitative Analysis
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Reposted 11 Hours AgoSaved
In-Office
Boston, MA, USA
118K-178K Annually
Mid level
118K-178K Annually
Mid level
Biotech • Pharmaceutical
The Quality Manager coordinates quality assurance activities, supports compliance for clinical and commercial QC operations, and leads improvements in cGMP processes involving gene therapy products.
Top Skills: Analytical MethodsCgmpElectronic Document Management SystemsQdoccsTrackwiseVeeva
Reposted 11 Hours AgoSaved
In-Office
Boston, MA, USA
200K-300K Annually
Expert/Leader
200K-300K Annually
Expert/Leader
Biotech • Pharmaceutical
Lead strategic and operational clinical pharmacology activities across programs, develop clinical pharmacology plans, guide PK/PD analyses and modeling, oversee clinical studies and regulatory documents, mentor staff, and support hiring.
YesterdaySaved
In-Office
Paddington, Westminster, London, England, GBR
Senior level
Senior level
Biotech • Pharmaceutical
The Director leads a team in forecasting, data analytics, and insights within the International Commercial organization, managing projects and enhancing program operations using AI and advanced analytics.
Top Skills: Advanced AnalyticsAi And AutomationCoding/ProgrammingData Warehouse SystemsExcelPower BI
Reposted YesterdaySaved
In-Office
Boston, MA, USA
163K-244K Annually
Senior level
163K-244K Annually
Senior level
Biotech • Pharmaceutical
The Associate Director will develop and execute digital marketing strategies for healthcare professionals, ensuring compliance and leveraging digital tools to enhance engagement and communication.
Top Skills: Ai StrategiesCrm SystemsDigital Marketing ToolsPredictive Analytics
Reposted YesterdaySaved
In-Office
Boston, MA, USA
141K-211K Annually
Senior level
141K-211K Annually
Senior level
Biotech • Pharmaceutical
The Principal Research Scientist will lead the Dissolution Team in drug development, mentor members, conduct dissolution studies, and ensure compliance with regulatory guidelines.
Top Skills: Analytical ChemistryFda GuidelinesFormulation DevelopmentIch GuidelinesRegulatory Submissions
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