Senior Clinical Research Associate

Upsilon Global · Italia, Italia ·


Descrizione dell'offerta

Upsilon Global are seeking a freelance CRA based in Italy to perform remote monitoring visits and site management activities across 5 sites for a cardiology study.


This is estimated to be 0.5 FTE, starting in October and working with an expanding CRO with operations across US, EU and APAC regions.


Regulatory and start-up activities have been performed and we now need a local expert to take over for the main monitoring activities.


Key information:

Position: Freelance CRA

FTE: 0.5 FTE

Indication: Cardiology

Start Date: October 2025

Travel: Remote monitoring for 5 sites across Italy

Location: Italy


Key Responsibilities :

  • Conduct remote visits, monitoring and assessment of clinical trial site, ensuring adherence to study protocols, Good Clinical Practice (GCP) guidelines, and applicable regulatory requirements.
  • Perform source document verification, data collection, and accurate recording of study data, ensuring data integrity and compliance.
  • Collaborate with site investigators, site staff, and study team members to ensure successful execution of clinical trials.
  • Assist in the development and review of study documents, including protocols, informed consent forms, and case report forms.
  • Maintain effective communication with study site, sponsors, and other stakeholders to provide timely updates, address queries, and resolve issues.
  • Monitor subject safety, reporting adverse events, and ensuring appropriate follow-up actions are taken.
  • Contribute to the preparation and coordination of study initiation, monitoring, and close-out activities.
  • Assist in the preparation and participation in regulatory inspections and audits as necessary.
  • Stay updated with current regulations, guidelines, and industry trends related to clinical research in translational/early-phase trials


Experience:

  • 5+ years independent monitoring experience
  • A strong background in cardiology trials
  • In-depth knowledge of local regulatory requirements and clinical trial processes.
  • Strong organizational and communication skills, with the ability to manage multiple priorities.
  • Ability to work independently, demonstrating initiative, attention to detail, and problem-solving skills


For more information, please apply via the link or contact

Candidatura e Ritorno (in fondo)