Milan-Based Site Activation Specialist – Clinical Trials

IQVIA; Milano; In loco; EUR 33.000 - 49.000; Tempo pieno

Vantaggi offerti da questo lavoro

Exposure across 21 Therapeutic Areas

Global team across 141 locations

Access to new technologies

Collaborative environment

Descrizione del lavoro

IQVIA’s Global Site Activation team in Milan, Italy drives site activation for clinical trials to ensure timely patient access to therapies. The Site Activation Specialist serves as the single point of contact for feasibility, activation and maintenance tasks, coordinating with project management and other departments to ensure regulatory and contractual accuracy.

The role requires a Life Science degree and 2–3 years in clinical research/site activation, with strong regulatory knowledge,

Competenze

• Bachelor’s degree in Life Science or allied field.
• 2–3 years’ experience in clinical research or site activation.
• Experience with regulatory submissions.
• Ability to work independently and with others.
• Demonstrated leadership and interpersonal skills.
• Strong communication and organizational abilities for cross-functional collaboration.
• Ability to handle multiple projects simultaneously.
• Knowledge of local regulations, SOPs, ICH/GCP.

Mansioni

• Serve as a Single Point of Contact for feasibility, site activation and maintenance activities in assigned studies.
• Review documents for completeness, accuracy, and consistency; prepare site documents and inform team members upon completion.
• Update and maintain internal systems, databases, tracking tools, timelines and project plans with accurate information.
• Review, track and follow up on regulatory, ethics, ICF and Investigator Pack release documents.

Conoscenze

Independent work

Leadership

Communication

Organizational skills

Multi-project management

ICH/GCP knowledge

Documentation

Regulatory understanding

Formazione

Bachelor’s Degree in Life Science

Descrizione del lavoro

IQVIA’s Global Site Activation team in Milan, Italy drives site activation for clinical trials to ensure timely patient access to therapies. The Site Activation Specialist serves as the single point of contact for feasibility, activation and maintenance tasks, coordinating with project management and other departments to ensure regulatory and contractual accuracy.

The role requires a Life Science degree and 2–3 years in clinical research/site activation, with strong regulatory knowledge,