
Senior Pharmacovigilance Reporting Associate
3 weeks ago
Senior Pharmacovigilance Reporting Associate ICON plc is a world-leading healthcare intelligence and clinical research organization We re proud to foster an inclusive environment driving innovation and excellence and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Senior Pharmacovigilance Reporting Associate to join our diverse and dynamic team As a Senior Pharmacovigilance Reporting Associate at ICON you will be essential in ensuring accurate and timely reporting of safety data related to pharmaceutical products You will work closely with cross-functional teams to enhance the organization s pharmacovigilance reporting processes and maintain compliance with regulatory standards What You Will Be Doing Preparing and submitting adverse event reports and safety data in accordance with regulatory requirements and internal policies ensuring accuracy and completeness Collaborating with clinical and regulatory teams to review and analyze safety data identifying trends and potential safety signals for further investigation Assisting in the preparation of periodic safety update reports PSURs annual reports and other regulatory documents to ensure compliance with reporting obligations Monitoring timelines for safety report submissions and proactively managing any delays or issues that may arise in the reporting process Maintaining and updating pharmacovigilance databases ensuring the integrity and quality of safety data through meticulous data entry and validation Providing training and support to junior team members on reporting procedures and pharmacovigilance regulations to enhance team capabilities Engaging in audits and inspections by regulatory authorities ensuring readiness and adherence to all relevant pharmacovigilance reporting requirements Staying informed about changes in regulatory guidelines and industry standards to ensure ongoing compliance and best practices in pharmacovigilance reporting Your Profile Bachelor s degree in life sciences pharmacy or a related field An advanced degree is preferred Extensive experience in pharmacovigilance or drug safety reporting with a strong understanding of relevant regulations and guidelines Proven ability to prepare and submit accurate adverse event reports and safety data in a timely manner Strong analytical skills with the ability to interpret safety data and identify trends or issues requiring further action Excellent communication and interpersonal skills with the ability to work collaboratively in cross-functional teams Proficiency in pharmacovigilance databases and reporting tools as well as Microsoft Office Suite Ability to manage multiple projects and priorities in a fast-paced environment while maintaining attention to detail Commitment to maintaining confidentiality and handling sensitive patient information with discretion What ICON can offer you Our success depends on the quality of our people That s why we ve made it a priority to build a diverse culture that rewards high performance and nurtures talent In addition to your competitive salary ICON offers a range of additional benefits Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family Our benefits examples include Various annual leave entitlements A range of health insurance offerings to suit you and your family s needs Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead Global Employee Assistance Programme TELUS Health offering 24-hour access to a global network of over 80 000 independent specialised professionals who are there to support you and your family s well-being Life assurance Flexible country-specific optional benefits including childcare vouchers bike purchase schemes discounted gym memberships subsidised travel passes health assessments among others Visit our to read more about the benefits ICON offers At ICON inclusion belonging are fundamental to our culture and values We re dedicated to providing an inclusive and accessible environment for all candidates ICON is committed to providing a workplace free of discrimination and harassment All qualified applicants will receive equal consideration for employment without regard to race color religion sex sexual orientation gender identity national origin disability or protected veteran status If because of a medical condition or disability you need a reasonable accommodation for any part of the application process or in order to perform the essential functions of a position please let us know or submit a request Interested in the role but unsure if you meet all of the requirements We would encourage you to apply regardless - there s every chance you re exactly what we re looking for here at ICON whether it is for this or other roles Are you a current ICON Employee Please click to apply
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Senior Pharmacovigilance Reporting Associate
2 days ago
Chennai, Tamil Nadu, India ICON plc Full time ₹ 9,00,000 - ₹ 12,00,000 per yearSenior Pharmacovigilance Reporting AssociateICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical developmentWe are currently seeking a Senior Pharmacovigilance...
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Supervisor, Pharmacovigilance
2 weeks ago
Chennai, Tamil Nadu, India ICON plc Full time ₹ 10,00,000 - ₹ 25,00,000 per yearPV Supervisor ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Supervisor, Pharmacovigilance to join our diverse and...
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Senior Associate, External Reporting
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OTC Derivatives Regulatory Reporting Associate
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Chennai, Tamil Nadu, India Teamware Solutions Full time ₹ 6,00,000 - ₹ 12,00,000 per yearAssociate – OTC Derivatives Regulatory Reporting We are looking for a detail-oriented Associate – OTC Derivatives Regulatory Reporting to join our team in Chennai. The role involves managing day-to-day reporting of OTC derivatives transactions, valuations, and collateral to DTCC under multiple regulatory frameworks. You will work closely with global...
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Business Intelligence Senior Associate
2 days ago
Chennai, Tamil Nadu, India NTT DATA, Inc. Full time ₹ 17,50,000 - ₹ 25,00,000 per yearRole Overview:The Business Intelligence Senior Associate will be responsible for transforming data into actionable insights that drive business decisions. The role involves managing BI tools, developing dashboards, ensuring data accuracy, and collaborating with business and technical teams to deliver data-driven strategies.Key Responsibilities:Design,...
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Reporting Analyst
1 week ago
Chennai, Tamil Nadu, India SHELL Full time ₹ 9,00,000 - ₹ 12,00,000 per yearJob Description Location: India Job Family Group: Finance Worker Type: Regular Posting Start Date: August 29, 2024 Business Unit: Finance Experience Level: Early Careers :Understanding all Shell internal group reporting and analysis requirements for Holdings and Treasury entities whilst ensuring key controls and reconciliations are...
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Senior Finance Associate
2 hours ago
Chennai, Tamil Nadu, India Zocket Technologies Private Limited Full time ₹ 1,20,000 - ₹ 6,00,000 per yearSenior Finance Associate – USLocation: ChennaiExperience: 4–5 yearsWe are looking for a highly skilled and detail-oriented Senior Finance – US to support and manage our finance operations for the US entity. The ideal candidate will have strong experience in US bookkeeping, tax compliance, and financial reporting, along with the ability to lead...