Global Site Activation Expert - Accelerate Clinical Trials

IQVIA LLC

Madrid

On-site

EUR 42,000 - 64,000

Full time

2 days ago

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Benefits offered by this job

Exposure across 21 Therapeutic Areas

Be part of a global team across 141+?

Exposure across a variety of studies

Access to new technologies

Collaborative and vibrant environment

Job summary

IQVIA’s Global Site Activation team in Spain is seeking a Site Activation Specialist to act as a single point of contact for feasibility, site activation and maintenance across studies, ensuring regulatory and SOP compliance. You will review regulatory and contract documents and coordinate with cross-functional teams to keep project plans current.

The role requires a Bachelor’s degree in Life Science or related field and a minimum of three years in clinical research, with strong communication

Qualifications

Bachelor’s Degree in Life Science or related field.
Minimum of 3 years’ prior experience in Clinical Research.
Experience with submissions to Ethics Committees and Regulatory Authorities, contract and budget negotiations, and start-up activities.
Familiarity with day-to-day responsibilities within Global Site Activation and related processes.
Ability to work independently but also collaborate with others.
Strong interpersonal, communication and organizational skills.

Responsibilities

Serve as a Single Point of Contact to perform feasibility, site activation and maintenance activities in assigned studies.
Review documents for completeness, consistency, and accuracy under guidance of senior staff.
Coordinate with Site Activation Manager, Project Management and other departments.
Update and maintain internal systems, databases, tracking tools, timelines and project plans with accurate information.