Operations Specialist 1 JLPT

Job Description As a Safety Data Processing Specialist at IQVIA, your role will involve reviewing, assessing, and processing safety data and information from various sources. You will distribute reports to internal and external parties in compliance with regulations, SOPs, and project requirements. Your key responsibilities will include: - Prioritizing and completing assigned trainings on time - Processing safety data according to regulations and guidelines - Performing pharmacovigilance activities such as collecting adverse events information, database entry, and coding - Ensuring quality and productivity standards are met - Identifying and addressing quality problems - Communicating with different team members to address project issues - Attending project team meetings and providing feedback - Leading or supporting department initiatives - Ensuring compliance with all people practices and processes Additionally, depending on project requirements, you may be involved in medical review activities. Your qualifications should include: - Bachelor's degree in a scientific or healthcare discipline - Up to 3 years of relevant experience - Good knowledge of medical terminology - Working knowledge of safety databases and relevant applications - Understanding of global, regional, and local clinical research regulatory requirements - Excellent attention to detail and accuracy - Proficiency in Microsoft Office and web-based applications - Strong organizational and time management skills - Effective verbal and written communication skills - Ability to work independently and as part of a team - Willingness to learn new skills and adapt to changing demands - Strong commitment to quality and integrity IQVIA is a leading global provider of clinical research services and healthcare intelligence. They are committed to integrity in the hiring process and maintain a zero-tolerance policy for candidate fraud. For more information, visit https://jobs.iqvia.com. As a Safety Data Processing Specialist at IQVIA, your role will involve reviewing, assessing, and processing safety data and information from various sources. You will distribute reports to internal and external parties in compliance with regulations, SOPs, and project requirements. Your key responsibilities will include: - Prioritizing and completing assigned trainings on time - Processing safety data according to regulations and guidelines - Performing pharmacovigilance activities such as collecting adverse events information, database entry, and coding - Ensuring quality and productivity standards are met - Identifying and addressing quality problems - Communicating with different team members to address project issues - Attending project team meetings and providing feedback - Leading or supporting department initiatives - Ensuring compliance with all people practices and processes Additionally, depending on project requirements, you may be involved in medical review activities. Your qualifications should include: - Bachelor's degree in a scientific or healthcare discipline - Up to 3 years of relevant experience - Good knowledge of medical terminology - Working knowledge of safety databases and relevant applications - Understanding of global, regional, and local clinical research regulatory requirements - Excellent attention to detail and accuracy - Proficiency in Microsoft Office and web-based applications - Strong organizational and time management skills - Effective verbal and written communication skills - Ability to work independently and as part of a team - Willingness to learn new skills and adapt to changing demands - Strong commitment to quality and integrity IQVIA is a leading global provider of clinical research services and healthcare intelligence. They are committed to integrity in the hiring process and maintain a zero-tolerance policy for candidate fraud. For more information, visit https://jobs.iqvia.com.