Site Activation Specialist: Catalyze Clinical Trial Sites

IQVIA

Milano

In loco

EUR 33.000 - 49.000

Tempo pieno

2 giorni fa
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Vantaggi offerti da questo lavoro

Exposure across therapies
Global team across locations
Innovative technologies
Collaborative environment
Own your career

Descrizione del lavoro

IQVIA is seeking a Site Activation Specialist in Milan, Italy. You will act as the single point of contact for feasibility, site activation, and maintenance across assigned studies, coordinating with the Site Activation Manager and project teams.

You will review regulatory documents, prepare site paperwork, and ensure timely updates across systems, timelines, and plans while managing multiple projects and regulatory requirements.

Competenze

  • Bachelor’s Degree in Life Science.
  • 2–3 years of prior experience in clinical research / site activation.
  • Experience of regulatory submissions essential.
  • Ability to work independently but also collaborate with others.
  • Leadership skills.
  • Good interpersonal, communication and organisational skills to establish and maintain effective working relationships with co-workers, managers and sponsors.
  • Ability to work on multiple projects.
  • Knowledge of applicable regulatory requirements, including local regulations, SOPs and ICH/ GCP.

Mansioni

  • Serve as a Single Point of Contact to perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions.
  • Review documents for completeness, consistency, and accuracy, under guidance of senior staff and prepare site documents, inform team members of completion of regulatory contracts.
  • Distribute completed documents to sites and internal project team members and update and maintain internal systems, databases, tracking tools, timelines, and project plans with accurate and complete project specific information.
  • Review, track, and follow up the progress, the approval and execution of required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Form, and Investigator Pack release documents.

Conoscenze

Leadership skills
Independent work
Interpersonal skills
Communication skills
Organizational skills
Project management

Formazione

Bachelor’s Degree in Life Science

Descrizione del lavoro

IQVIA is seeking a Site Activation Specialist in Milan, Italy. You will act as the single point of contact for feasibility, site activation, and maintenance across assigned studies, coordinating with the Site Activation Manager and project teams.

You will review regulatory documents, prepare site paperwork, and ensure timely updates across systems, timelines, and plans while managing multiple projects and regulatory requirements.

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