Clinical Research Assistant Internship

2 settimane fa


Verona, Veneto, Italia Alira Health A tempo pieno
Job Description

We are seeking a Clinical Trial Coordinator Intern to assist our clinical research team in conducting studies according to GCP, SOP, protocol, and respecting budget and timelines.

Key Responsibilities:
  1. Assist with start-up activities, including ethical and regulatory submissions, and sites contracts negotiation.
  2. Prepare and maintain ISF documents and TMF setup (under PM oversight).
  3. Maintain relationships with Ethics Committees and Contracting Authorities.
  4. Support site/vendors invoicing management and maintain tracking if required.
  5. Collaborate in the preparation of weekly/monthly project reports and update CTMS and study-specific trackers as needed.
  6. Support CRAs activities follow-up.
  7. Support document translation if required.
  8. Participate in internal, client/sponsor, scientific, and other meetings as required; participate in audits.
  9. Perform additional duties as assigned.
Desired Qualifications and Experience:
  1. Bachelor's degree in a scientific or health-related field.
  2. Previous experience in clinical research (in CROs, Pharma, or academy/hospital setting).
  3. Good knowledge of ICH GCP and appropriate regulations.
  4. Good knowledge of Clinical Research and Regulatory/Ethical requirements.
Technical Competences and Soft Skills:
  1. English language proficiency.
  2. Proficiency in MS Office Suite.
  3. Professionalism, trustworthiness, and quality focus.
  4. Strong analytical and organizational skills.
  5. Excellent communication and interpersonal skills with customer service orientation.


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