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Lead lab operations by enhancing efficiency, managing projects, ensuring data integrity, and supporting clinical trials through effective programming and analysis.

Support Marketing and Sales to generate campaigns and leads, analyze opportunities, schedule introductory business development calls, respond to inbound web leads, track prospect/client activity in CRM, and collaborate with sales leaders to develop market strategies across Parexel service lines.

The Clinical Project Manager oversees project planning and execution, ensuring timely updates and coordination of project milestones within clinical operations.

Lead country/regional study operations from startup through close, overseeing CROs and site activation, managing timelines, budgets, risks, recruitment, vendor deliverables, and resolving escalations to ensure timely study delivery and compliance.

The Meeting Specialist will manage pharmaceutical meeting logistics, ensuring compliance and high-quality experiences for stakeholders while overseeing project execution and finance management.

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.

Manage design, configuration, launch, monitoring, and close-out of electronic feasibility surveys. Ensure site/investigator readiness, maintain contact lists, track responses and CDAs, apply site identification strategy, and support risk mitigation for global feasibility assessments.

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.

The Clinical Laboratory Study Manager manages clinical trial sample operations, ensures compliance, oversees data management, and liaises with various stakeholders to support biomarker evaluation.

The Manager, Data Analysis oversees centralized monitoring for clinical trials, ensuring effective RBQM systems, data analysis, and reporting while collaborating with cross-functional teams.