Job Description:
A Clinical Operations Consultant in Geneva works with healthcare providers, research institutions, and pharmaceutical companies to optimize clinical workflows and trial management. The consultant evaluates operational efficiency, compliance with clinical standards, and patient care models. This role is essential in Geneva’s highly regulated healthcare and life sciences sectors. Responsibilities include developing SOPs, improving trial timelines, managing site operations, and ensuring regulatory alignment. The consultant often supports cross-functional teams and assists with scaling operations in multinational clinical environments.
Job Requirement:
Degree in Life Sciences, Medicine, or Healthcare Management
Experience in clinical research, operations, or trial coordination
Strong knowledge of ICH-GCP, regulatory requirements, and SOP development
Excellent organizational and documentation skills
Familiarity with clinical trial systems and data management platforms
Fluent in English and French; German is a plus
Strong project management and risk assessment capabilities
Ability to liaise with CROs, sites, and regulatory bodies
Skilled in identifying and resolving operational bottlenecks
Detail-oriented with a focus on compliance and quality assurance
