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Reposted 13 Days AgoSaved
Remote
US
27-30 Hourly
Internship
27-30 Hourly
Internship
Biotech
As a Data Insights Intern, you will manage and transform data from clinical trials to support quality management, develop systems for data use, and generate insights for decision-making.
Top Skills: MsofficePower AutomatePowerappsPower BI
Reposted 13 Days AgoSaved
Remote
US
176K-236K Annually
Senior level
176K-236K Annually
Senior level
Biotech
Lead Global Clinical Operations compliance activities, ensuring ICH GCP and regulatory adherence. Develop risk management, root cause analysis, CAPA, inspection preparedness, and quality-by-design for clinical studies. Partner with cross-functional stakeholders to embed preventive compliance, monitor trends, escalate significant issues, and report compliance status to leadership.
Top Skills: ExcelOutlookPowerPointVisioWord
Reposted 13 Days AgoSaved
Remote
US
136K-181K Annually
Senior level
136K-181K Annually
Senior level
Biotech
The Senior Learning Business Partner in Global Clinical Operations focuses on developing technical and leadership capabilities, designing training programs, and ensuring alignment with regulatory standards.
Top Skills: Adult Learning PrinciplesClinical TrialsInstructional DesignLearning And DevelopmentRegulatory Requirements
13 Days AgoSaved
Remote
US
176K-236K Annually
Expert/Leader
176K-236K Annually
Expert/Leader
Biotech
The Director, Global Regulatory Project Management leads oncology regulatory strategies, ensuring successful global drug submissions, while driving operational excellence and collaboration across teams.
Top Skills: Electronic Document Management SystemsMicrosoft Office SuiteMs ProjectPower BIRegulatory Submission PlatformsSmartsheets
Reposted 13 Days AgoSaved
Remote
US
147K-197K Annually
Senior level
147K-197K Annually
Senior level
Biotech
The Associate Director is responsible for leading global regulatory project management, ensuring successful regulatory submissions, and facilitating cross-functional collaboration to maintain product market access worldwide.
Top Skills: MS OfficeMs ProjectPower BISmartsheets
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Reposted 13 Days AgoSaved
Remote
US
163K-213K Annually
Senior level
163K-213K Annually
Senior level
Biotech
Lead the Central Statistical Monitoring team, ensuring subject safety and data integrity in clinical trials through statistical analysis and collaboration with various stakeholders.
Top Skills: MS OfficePower BI
Reposted 13 Days AgoSaved
Remote
US
176K-236K Annually
Expert/Leader
176K-236K Annually
Expert/Leader
Biotech
The Director of Global Regulatory Project Management leads oncology regulatory strategies, ensures timely submissions, manages global project teams, and fosters cross-regional collaboration to maintain market access for products.
Top Skills: Electronic Document Management SystemsMicrosoft Office SuiteMs ProjectPower BISmartsheets
Reposted 13 Days AgoSaved
Remote
US
187K-247K Annually
Senior level
187K-247K Annually
Senior level
Biotech
Lead the Central Statistical Monitoring team to oversee statistical design and governance in clinical trials, ensuring data integrity and safety. Develop monitoring indicators, validate models, and communicate findings to cross-functional teams. Provide training and support for audits and inspections, promoting continuous improvement in statistical practices.
Top Skills: MS OfficePower BI
14 Days AgoSaved
Remote
US
142K-187K Annually
Mid level
142K-187K Annually
Mid level
Biotech
The Senior Manager will oversees clinical development programs, ensuring their execution stays on scope, budget, and timelines, while supporting various functional areas and collaborating with external partners.
Reposted 14 Days AgoSaved
Remote
US
179K-239K Annually
Senior level
179K-239K Annually
Senior level
Biotech
Lead and mentor program management for oncology development, execute projects, manage schedules, oversee budgets, and drive team efficiency.
Top Skills: ExcelMicrosoft WordOutlookProject
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