What are the responsibilities and job description for the Clinical Trial Consultant II position at TalentBurst, an Inc 5000 company?
US_Clinical Trial Consultant II
Duration: 12 months
Location: Cambridge, MA (Hybrid)
Description:
Duration – 1 Year
Number of Hours per week – 40 per week
Cambridge office : 2 days
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 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 : Bachelor's degree in science or healthcare related field
Experience : 4 years experience in pharmacovigilance
Salary : $55 - $60