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The Senior Biostatistician designs statistical strategies for clinical trials, performs analyses using SAS, and collaborates with study teams to ensure high-quality research and statistical deliverables.

Manage clinical safety operations related to adverse events, process reports, ensure compliance with regulations, supervise junior staff, and participate in audits and data reconciliation.

Manage and monitor clinical study sites according to guidelines, ensuring data integrity, compliance, and efficient resource use while interacting with internal teams.

The Clinical Start-Up & Trial Lead oversees clinical trial activities from start to finish, ensuring operational excellence and managing stakeholder communications.

The Sr. CRA 2 will monitor clinical trial sites, ensure compliance with protocols, manage study registry, and oversee data integrity while traveling frequently.

The Associate Clinical Data Manager leads data management activities for clinical studies, ensuring protocol compliance, project timelines, and quality deliverables. Responsibilities include managing project teams, client relationships, risk assessment, and mentorship of staff while adhering to industry standards and improving processes.

The role involves monitoring clinical trials, ensuring compliance with protocols, managing site documentation, and supporting investigators in study administration and regulatory adherence.

The Manager, Site Readiness oversees study start-up and maintenance operations, ensuring quality delivery and compliance while managing a startup team across country or clusters. They serve as the local expert on start-up processes, supporting team development and regulatory compliance, and coordination with clients and vendors.

The Screening Receptionist will manage participant check-in/check-out processes, maintain accurate records, provide front-desk support, and ensure compliance with documentation in a clinical research environment.

Lead clinical data management activities, ensure quality and timely deliverables, mentor junior staff, and maintain strong client relationships in clinical trials.