Clinical Research Analyst – Senior

Responsibilities

• Manage and oversee clinical study operations from start to finish:
• Participate in study start-up and operational management.
• Manage regulatory and study documentation, including working knowledge of CRF, eTMF/TMF and other systems used in clinical research.
• Interact with investigators, physicians and various internal departments to ensure proper progress of projects.

Requirements

• Bachelor's degree or higher;
• Fluent in English;
• Experience in clinical study operations;
• Familiarity with CRF, eTMF/TMF and relevant clinical systems.

Core Competencies

Demonstrates expertise in managing clinical study operations, including regulatory documentation and interaction with stakeholders. Proficient in utilizing clinical research systems such as CRF and eTMF/TMF to ensure project progress.

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