Pharmacovigilance - ICSR Case Processing
Job Title: Pharmacovigilance - ICSR Case Processing
Location: Cambridge, MA 02142/Hybrid- 2 days Office
Duration: 12 Months+ (Possible Extension)
Pay Range - $50 - $60/hr. on w2
Job Product
Responsible for case processing and/or QC of clinical trial ICSRs and post market case processing from sanctioned countries.
Key Responsibilities:
ā¢ Triage, Intake, case entry and QC of ICSRs originating from *** sponsored studies or other assigned cases
ā¢ Includes narrative writing, MedDRA coding, drafting of follow-up queries and event notifications to internal stakeholders
ā¢ Perform retrospective quality checks on processed cases
ā¢ 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
ā¢ Review and resolution of reconciliation issues between the clinical and safety databases per in collaboration with Data Management
ā¢ Provide investigation details into late regulatory reporting of CT (Clinical Trials) cases
Essential Skills and Qualifications Required:
ā¢ Knowledge of Global and local safety regulations
ā¢ Excellent written and verbal communication skills
ā¢ Experience in ICSR processing in safety database systems such as ArisG, Argus and Veeva
ā¢ Understanding of global safety reporting regulations and guidelines including the FDA, ICH, and EU Regulations and Requirements for Pharmacovigilance
ā¢ Strong computer skills within Microsoft suite of programs (Word, Excel, PowerPoint, and Outlook)
ā¢ Knowledge of medical and clinical practices and a strong understanding of medical concepts and terminology required
Education and Experience Requirements for Job:
Education : Bachelor's degree in science or healthcare related field
Experience : 4+ years' experience in pharmacovigilance
Apply Now
Apply Now
Location: Cambridge, MA 02142/Hybrid- 2 days Office
Duration: 12 Months+ (Possible Extension)
Pay Range - $50 - $60/hr. on w2
Job Product
Responsible for case processing and/or QC of clinical trial ICSRs and post market case processing from sanctioned countries.
Key Responsibilities:
ā¢ Triage, Intake, case entry and QC of ICSRs originating from *** sponsored studies or other assigned cases
ā¢ Includes narrative writing, MedDRA coding, drafting of follow-up queries and event notifications to internal stakeholders
ā¢ Perform retrospective quality checks on processed cases
ā¢ 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
ā¢ Review and resolution of reconciliation issues between the clinical and safety databases per in collaboration with Data Management
ā¢ Provide investigation details into late regulatory reporting of CT (Clinical Trials) cases
Essential Skills and Qualifications Required:
ā¢ Knowledge of Global and local safety regulations
ā¢ Excellent written and verbal communication skills
ā¢ Experience in ICSR processing in safety database systems such as ArisG, Argus and Veeva
ā¢ Understanding of global safety reporting regulations and guidelines including the FDA, ICH, and EU Regulations and Requirements for Pharmacovigilance
ā¢ Strong computer skills within Microsoft suite of programs (Word, Excel, PowerPoint, and Outlook)
ā¢ Knowledge of medical and clinical practices and a strong understanding of medical concepts and terminology required
Education and Experience Requirements for Job:
Education : Bachelor's degree in science or healthcare related field
Experience : 4+ years' experience in pharmacovigilance
Apply Now
Apply Now