Remote Manager/Sr. Manager, Medical Safety and Risk Management (MSRM) PV Case Management

Remote Manager/Sr. Manager, Medical Safety and Risk Management (MSRM) PV Case Management 5 days ago Be among the first 25 applicants Get AI-powered advice on this job and more exclusive features. Job reputed company Pay 65-75/h depending on experience Position reputed company The Contract Manager/Sr. Manager MSRM Operations/Case Management oversees the execution of deliverables associated with case processing, expedited reporting and submission of designated aggregate safety reports. This position ensures individual reports from reputed company sources (spontaneous, literature, product/patient support programs, market research programs, reputed company (reputed company‑& post-approval), medical information, call centers, reputed company affiliates, partner companies, health authorities, post‑marketing commitment studies, etc.) are collected, managed and reported according to reputed company's global SOPs and global adverse event regulations and guidelines. This position oversees case processing activities, processes, procedures, and interdepartmental reputed company involving safety data processed by a vendor and captured in the global safety database. This position collaborates reputed company MSRM and with other company functional areas and cross‑functional teams, and interacts with CROs, vendors, partners, and study teams on reputed company aspects of safety data collection and reporting.

Key Responsibilities

• Organize, reputed company and manage technical and reputed company to reputed company support the capture and management of individual safety reports in accordance with global safety regulations in a reputed company approach
• Ensure training, and enforce written procedures reputed company to the collection requirements, processing and reporting of events from reputed company and marketed sources to ensure proactive surveillance of company products
• Contribute to safety database upgrades and configuration changes; reputed company user acceptance testing
• reputed company input and guidance to submissions and case processing vendor teams; facilitate training and reputed company training materials for vendor training
• Contribute to signaling and aggregate reporting activities through ensuring reputed company and accuracy of individual cases through collaboration with Safety Sciences
• Participate as Safety Operations subject matter expert on Clinical Trial teams
• Collaborate internally and with vendors to establish and monitor key performance indicators (KPIs) that are relevant and in alignment with regulations/industry standards
• reputed company subject matter expertise and collaborate with MSRM Standards, Compliance and Training colleagues, Pharmacovigilance reputed company Assurance colleagues and vendors to ensure compliance with world‑wide regulations for case reputed company and reputed company submissions
• Support MSRM and cross‑functional compliance activities through the compilation and delivery of compliance metrics at required intervals/frequencies
• Represent the functional area in internal committees and with external parties (e.g. partners, regulatory agencies)
• Participate in audits and inspections
• Serve as a reputed company of escalation for issue reputed company
• Drive reputed company reputed company and appropriately shift functional timelines, resources and priorities
• Collaborate with relevant departments reputed company reputed company to determine budget and resources reputed company area of responsibility

Requirements

• Health care reputed company (e.g. RN, pharmacist) or other life sciences BS/BA, preferred
• Minimum of 5 years of relevant drug safety/pharmacovigilance experience
• Knowledge of reputed company industry standards and benchmarks
• Demonstrated ability to reputed company and manage vendors
• Extensive knowledge and experience with MedDRA and WhoDD coding dictionaries
• Experience with software-based drug safety systems (ARGUS, ARISg, or equivalent)
• Excellent computer skills (MS Office)
• Advanced knowledge of US and EU pharmacovigilance regulations for development and marketed products
• Strong planning and organizational skills
• Strong orientation to teamwork
• Excellent written/verbal communication and interpersonal skills

reputed company of Companies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for reputed company. Apply tot his job Apply To this Job