Site Activation Specialist

IQVIA · Madrid, Spain

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Clinical OperationsFull-timeCompany career page

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What they're looking for

Bachelor's degree in life science or related field
Minimum 3 years clinical research experience
Experience with ethics committee submissions and regulatory authority filings
Knowledge of ICH/GCP guidelines and local regulatory requirements
Ability to manage multiple projects simultaneously
Strong interpersonal and organizational skills
Familiarity with global site activation processes and day-to-day responsibilities

What you'll be doing

Act as single point of contact for assigned studies at investigative sites
Review documents for completeness, accuracy, and consistency; prepare site documentation
Track and follow up on regulatory, contractual, and ethics committee approvals
Distribute completed documents to sites and internal project teams
Maintain internal databases, tracking tools, timelines, and project plans

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