Lead Consultant - Life Sciences

Longfinch Technologies

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, protocol development, site selection, patient recruitment, monitoring, and study close-out.
Knowledge of clinical trial data elements, Pharmacokinetics (PK), Pharmacodynamics (PD), modeling and simulation, and statistical analysis.
Familiarity with clinical research processes and regulatory frameworks.
Exposure to clinical trial data standards and domains.

Nice-to-Have Skills

Experience with metadata structures, Case Report Forms (CRFs) design, and data capture flows.
Understanding of clinical endpoints, biomarkers, and advanced statistical analysis concepts.

Experience & Certifications

Minimum 10+ years of relevant experience in Life Sciences and clinical trials.
Certifications: Not required

Apply

Vacancy posted 3 hours ago

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