Profile

  • Case management of post marketing ICSRs (e.g., consumer, doctor, literature, , regulatory)
  • Case management of clinical trial (Phase II , III)
  • Understanding of 15 days and 90 days reporting of all cases.
  • Hands on experience on any one of the safety database (Argus, Aris G, AB cube, Veeva)
  • Understanding of serious, non-serious case and SUSAR
  • Minimum 1-2 years of MedDRA coding and narrative writing experience.
  • Minimum 1-2 years’ experience in data entry, triaging of cases, follow-up of case request

Qualification

Experience: 2-6 years of experience in pharmacovigilance, case management and clinical trial

Knowledge: EU GVP, ICH and WHO guidelines

Education: life science, Pharmacy, medicine.

Country : Italy

Case Management Freelancer