Clinical Trial Coordinator Internship

2 settimane fa


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

A Clinical Trial Coordinator Intern assists the clinical research team in ensuring the conduct of studies in accordance with GCP, SOP, protocol, and budget and timelines. The role is responsible for start-up activities and document management.

Key Responsibilities
  1. Responsible for start-up activities, including Ethic and Regulatory submission, and sites contracts negotiation under PM oversight.
  2. Responsible for ISF preparation and TMF setup and maintenance under PM oversight.
  3. Maintains relationships with ECs and CA.
  4. Supports sites and vendors invoicing management and tracks appropriately.
  5. Collaborates with weekly/monthly and ad-hoc project reports preparation and updates CTMS and study-specific trackers as needed.
  6. Supports CRAs activities follow-up.
  7. Supports document translation if required.
  8. Participates in internal, client/sponsor, scientific, and other meetings as required and participates in audits.
  9. Performs additional duties assigned.
Desired Qualifications and Experience
  1. Graduation in a scientific/health field.
  2. Previous experience in clinical research in CROs, Pharma, or academia/hospital experience.
  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, good.
  2. MS Office Suite, good.
  3. Professional.
  4. Trustworthy.
  5. Quality-focused; ability to be careful, thorough, and detail-oriented.
  6. Strong organizational skills and ability to multi-task and work effectively in a fast-paced environment.
  7. Strong analytical skills.
  8. Strong communication and interpersonal skills with customer service orientation.
Languages

English

Education

Bachelor of Science (BS): Life Sciences, Bachelor of Science (BS): Pharmacy

Contract Type

Apprentice (Fixed Term)



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