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The Office Manager coordinates office activities, manages vendor relationships, oversees budgets, ensures health and safety compliance, and supports the Country Manager with administrative tasks.

Communicate with sponsors/CROs, track patient enrollment, maintain documents, ensure data entry accuracy, and support audits for clinical studies.

The Lead Site Coordinator manages clinical trial activities, oversees site staff, ensures compliance, recruits patients, and supports study protocol implementation.

Support clinical research projects by managing communication, documents, and supplies, coordinating audits, and maintaining tracking systems.

The Site Coordinator facilitates communication between Sponsors or CROs and clinical study sites, supports monitoring visits, tracks patient enrollment, manages regulatory documents, and aids in budget negotiations.

The role supports clinical research projects by managing documents, maintaining databases, coordinating inquiries, and ensuring efficient communication with sites and vendors.

As a Principal Statistician, you will lead statistical activities for global clinical trials, conduct analyses, develop protocols, and guide teams of statisticians and programmers.

The Site Coordinator facilitates communication between study sites and sponsors, tracks patient enrollment, handles regulatory documents, and supports study procedures and audits.

Lead biostatistical activities for global clinical trials, ensuring statistical integrity and communication across teams while managing statistical deliverables and training staff.

The Site Coordinator manages clinical trial activities, serves as a liaison between sponsors and sites, tracks enrollment, and ensures regulatory compliance.