External Job Description**Job Overview****Key Responsibilities**- Process Safety data as per regulations, guidelines, SOPs, and project requirements.- Perform Pharmacovigilance activities, including collecting and tracking incoming Adverse Events (AE)/endpoint information, database entry, coding AE and Products, writing narratives, and more.- Assess Safety data for reportability to relevant authorities and report within timelines.- Contribute to or lead deliverables in the field of Safety Publishing, Risk Management, Safety Surveillance, and Medical Information.- Ensure quality, productivity, and delivery standards are met.- Build a positive team environment, provide training and mentoring for less experienced team members.- Provide technical and process information to Safety Management and operational team on project-specific issues.- Maintain a thorough understanding of project protocol, therapeutic indication, budget, and scope of work (SOW) for assigned projects.- Attend project team meetings and provide regular feedback/inputs to Operations team manager on operational project metrics, challenges, and successes.- Contribute to the achievement of departmental goals.**Qualifications**- Bachelor's Degree in a scientific or healthcare discipline or allied life sciences.- Up to 4 years of relevant experience, inclusive of up to 2 years of Pharmacovigilance experience.- Excellent knowledge of medical terminology.- Excellent organizational skills, time management skills, attention to detail, and accuracy.- Proven ability to work independently and autonomously with policies and practices.- Ability to work effectively on multiple projects simultaneously, organize own workload, and effectively manage teams' priorities.- Flexibility to operate in shifts.LI-Remote