Top Tech Jobs & Startup Jobs in Charlotte, NC

Reposted 8 Minutes AgoSaved
Remote
United States
Senior level
Senior level
Pharmaceutical
The Sr. Contracts Specialist amends, negotiates, and finalizes project budgets and contractual documents, ensuring quality deliverables and client interactions for Parexel's projects.
Top Skills: DatabasesExcelOutlookWindowsWord
3 Days AgoSaved
Remote
United States
Senior level
Senior level
Pharmaceutical
The Senior Study Contract Manager is responsible for negotiating and managing contracts and budgets for clinical trials, ensuring compliance with guidelines and facilitating communication with stakeholders.
Top Skills: Clinical Study ManagementGdpGmpIch-Gcp
9 Days AgoSaved
Remote
United States
Senior level
Senior level
Pharmaceutical
The Regulatory Affairs Consultant guides clinical studies through regulatory requirements, advising teams on compliance and strategies for efficient trial execution. They engage with health authorities, manage communication, and ensure quality documentation.
Top Skills: Fda RegulationsGlobal Health Authority Regulations
Reposted 9 Days AgoSaved
Remote
United States
Senior level
Senior level
Pharmaceutical
The Senior Clinical Research Associate manages clinical trial sites, ensures adherence to regulations, oversees study conduct, and resolves issues while safeguarding patient safety.
Top Skills: DatabasesGood Clinical Practices
9 Days AgoSaved
Remote
United States
Expert/Leader
Expert/Leader
Pharmaceutical
The Executive Director, HEOR Modeling leads HEOR consulting projects, manages staff, ensures client satisfaction, and drives AI integration in HEOR while overseeing business development and strategic planning.
Top Skills: AIData AnalyticsHealth EconomicsMachine LearningNatural Language ProcessingPredictive Modeling
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10 Days AgoSaved
Remote
United States
Senior level
Senior level
Pharmaceutical
The Senior Regulatory Consultant will oversee regulatory strategies, manage complex timelines, enhance team performance, and guide regulatory projects to support the development of transformative therapies.
Top Skills: EctdMicrosoft Office SuiteSmartsheetVeeva Regulatory Information Management
Reposted 10 Days AgoSaved
Remote
United States
Senior level
Senior level
Pharmaceutical
As a Senior/Principal Regulatory Compliance Consultant, you will lead client engagements in QC Microbiology and sterile drug manufacturing, ensuring compliance and quality improvements while traveling extensively to support clients.
Top Skills: Aseptic ProcessingContamination ControlEnvironmental MonitoringMicrobial IdentificationQc Microbiology
Reposted 11 Days AgoSaved
Remote
United States
Junior
Junior
Pharmaceutical
The Senior Clinical Research Associate oversees site management and monitoring for clinical trials, ensuring compliance with GCP, patient safety, and quality execution of studies. Responsibilities include managing operational aspects, training site personnel, addressing protocol issues, and conducting monitoring activities.
Top Skills: Good Clinical Practices
Senior level
Pharmaceutical
The Senior Clinical Research Associate is responsible for site management and monitoring of clinical trials, ensuring compliance with regulations and quality standards, and enhancing investigator site relationships.
Top Skills: Good Clinical Practices (Gcp)
Reposted 13 Days AgoSaved
Remote
United States
Mid level
Mid level
Pharmaceutical
The Manager, Data Analysis oversees centralized monitoring for clinical trials, ensuring effective RBQM systems, data analysis, and reporting while collaborating with cross-functional teams.
Top Skills: MS OfficePythonRSASSQL
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