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Reposted 21 Days AgoSaved
Remote
US
27-30 Hourly
Internship
27-30 Hourly
Internship
Biotech
The intern will support analytical development and QC activities, conduct data analysis, and manage QC documents in a fast-paced, collaborative environment.
Top Skills: MS OfficeVeeva
Reposted 21 Days AgoSaved
Remote
US
27-27 Hourly
Internship
27-27 Hourly
Internship
Biotech
The intern will assist the QMS team in document review, authorship, compliance, and change control activities, ensuring document clarity and adherence to guidelines.
Top Skills: MS Office
Reposted 22 Days AgoSaved
Remote
US
167K-212K Annually
Senior level
167K-212K Annually
Senior level
Biotech
The Regional Business Manager will analyze market dynamics, drive sales strategies, lead training initiatives, and enhance leadership within the region to achieve business goals.
Top Skills: ExplorerGuruNavigator
Reposted 22 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 22 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
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22 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 22 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 22 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 22 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
23 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.
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