Job Description
Job Title: Clinical Trial Consultant II
Location: Cambridge, MA- Hybrid (2 days onsite)/open 100% remote
Duration: 1+ Year
Number of Hours per week: 40 per weeks
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 *** 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 an...
Location: Cambridge, MA- Hybrid (2 days onsite)/open 100% remote
Duration: 1+ Year
Number of Hours per week: 40 per weeks
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 *** 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 an...