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Reposted 5 Hours AgoSaved
Remote
United States
Senior level
Senior level
Pharmaceutical
The Sr. Clinical Research Associate manages sites for clinical trials, ensuring compliance with protocols and regulations, conducting monitoring visits, and collaborating with study teams.
Top Skills: EtmfGdpGmpIch-Gcp
Reposted 5 Hours AgoSaved
Remote
United States
Senior level
Senior level
Pharmaceutical
The Senior Clinical Research Associate manages study sites, ensuring compliance with regulations and high performance. Responsibilities include site selection, monitoring, training site staff, and data management.
Top Skills: CtmsEtmf
Reposted 5 Hours AgoSaved
Remote
United States
Senior level
Senior level
Pharmaceutical
Manage end-to-end labeling operations across global markets, ensure compliance with regulatory requirements, coordinate teams, and oversee drug safety activities.
Top Skills: Adobe AcrobatGlamsMS OfficePromomatsSharepointTrackwiseVeeva
Reposted 5 Hours AgoSaved
Remote
United States
Senior level
Senior level
Pharmaceutical
The Senior Regulatory Affairs Consultant will ensure compliance of promotional materials with US regulations, support product launches, and provide regulatory guidance across teams.
Top Skills: EdmsMS OfficeVeeva Promomats
Reposted 5 Hours 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
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Reposted 5 Hours AgoSaved
Remote
United States
Senior level
Senior level
Pharmaceutical
The Principal Biostatistician independently manages complex clinical trials, providing statistical support and leading studies with regulatory impact while contributing to business development and client interactions.
Top Skills: SAS
Reposted 5 Hours AgoSaved
Remote
United States
Mid level
Mid level
Pharmaceutical
Manage Regulatory CMC submissions, develop regulatory plans, coordinate projects, assist in health authority engagements, and ensure compliance with standards.
Top Skills: Microsoft Office SuiteSmartsheet
Reposted 5 Hours AgoSaved
Remote
United States
Mid level
Mid level
Pharmaceutical
As a Proposal Manager, you'll manage the proposal and contract processes, ensuring alignment with client specifications and collaborating across departments to deliver quality solutions on time.
Top Skills: DatabasesExcelOutlookSalesforceWindowsWord
Reposted 7 Hours AgoSaved
Remote
United States
Expert/Leader
Expert/Leader
Pharmaceutical
The Senior/Vice President, Technical will lead regulatory strategy initiatives, advise clients on product lifecycles, and represent Parexel as an industry thought leader while mentoring colleagues.
Top Skills: Clinical DevelopmentClinical Trial DesignRegulatory Applications
Reposted 7 Hours AgoSaved
Remote
United States
Senior level
Senior level
Pharmaceutical
Lead execution of complex publication programs in medical communications, manage projects, budgets, timelines, and collaborate with teams to ensure successful delivery.
Top Skills: Database ToolsExcelIenvisionMicrosoft WordOutlookPowerPoint
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