We are seeking a highly experienced Lead Consultant in Life Sciences with deep expertise in the end-to-end clinical trial lifecycle. The ideal candidate will have hands-on knowledge of clinical research processes, regulatory frameworks, and clinical trial data domains and standards.

Key Responsibilities

• Ensure clinical trial requirements align with regulatory, compliance, and industry standards.


• Lead functional requirements gathering and translate business needs into clear, actionable documentation.


• Create, maintain, and manage requirement artifacts for clinical studies.

Must-Have Skills & Expertise

• Strong expertise in the Life Sciences domain.


• In-depth understanding of clinical trial lifecycle, including study design, ...