Demo

Sr. Safety Associate

Planet Pharma
Cambridge, MA Contractor
POSTED ON 10/25/2026
AVAILABLE BEFORE 11/12/2027
Pay Range: $50-60/hr

  • depending on experience

Job Scope: Responsible for case processing and/or QC of clinical trial ICSRs and postmarket case processing from sanctioned countries.

Key Responsibilities

  • Triage, Intake, case entry and QC of ICSRs originating from Biogen sponsored studies or other assigned cases
  • Includes narrative writing, MedDRA coding, drafting of follow-up queries and event notifications to internal stakeholders
  • Perform retrospective quality checks on processed cases
  • Independently manage assigned cases, accounting for weekends and holidays, to deliver cases to internal stakeholders on time and ensure case completion allowing for on-time regulatory reporting
  • Review and resolution of reconciliation issues between the clinical and safety databases per in collaboration with Data Management
  • Provide investigation details into late regulatory reporting of CT cases

Essential Skills And Qualifications Required

  • Knowledge of Global and local safety regulations
  • Excellent written and verbal communication skills
  • Experience in ICSR processing in safety database systems such as ArisG, Argus and Veeva
  • Understanding of global safety reporting regulations and guidelines including the FDA, ICH, and EU Regulations and Requirements for Pharmacovigilance
  • Strong computer skills within Microsoft suite of programs (Word, Excel, PowerPoint, and Outlook)
  • Knowledge of medical and clinical practices and a strong understanding of medical concepts and terminology required

Education And Experience Requirements For Job

Education : Bachelors degree in science or healthcare related field

Experience : 4 years experience in pharmacovigilance

(No Value)

Salary : $50 - $60

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