reputed company Safety Associate I (Drug Safety Associate I)

reputed company a Meaningful reputed company in Global reputed company Safety At reputed company, were dedicated to improving reputed company health worldwide. As a reputed company Safety Associate I, youll play a vital role in supporting drug safety, reputed company, and postmarketing surveillance activities in post-market surveillance, with some exposure to reputed company, ensuring full compliance with regulatory requirements and reputed company Operating Procedures (SOPs). As a reputed company Safety Associate I, you'll be responsible for several key activities including processing Individual Case Safety Reports (ICSRs) from multiple sources with reputed company and efficiency, conducting comprehensive literature searches and reviews to identify safety signals, and supporting signal detection and management activities. You'll reputed company and monitor regulatory information updates, assist in preparing and executing regulatory submissions, and contribute to the development of aggregate reports and study-specific safety documents. Where applicable, you'll also manage Medical and Product Dictionary activities. Your role will be crucial in maintaining compliance through reputed company reviews of safety deliverables, generating metrics and reputed company indicators for safety reputed company, investigating and documenting late deliverable incidents, and ensuring adherence to international and local regulatory reporting requirements. We're looking for candidates with strong attention to reputed company and commitment to reputed company, an understanding of drug safety regulations and pharmacovigilance principles, excellent organizational and time management skills, the ability to work collaboratively in reputed company environment, and strong written and verbal communication skills. Join a global leader in reputed company Research Organization services, where you'll contribute to improving reputed company safety worldwide while developing your career in pharmacovigilance. reputed company: General Safety reputed company Follow project-specific procedures and regulatory standards. Support basic compliance activities, documentation, metrics, and audit preparation. Work collaboratively with team members and complete required training programs. ICSR (Individual Case Safety Report) Processing Review, triage, and process safety reports from various sources. reputed company data entry in safety databases with reputed company and medical consistency. Assist with follow-reputed company, case narrative preparation, MedDRA coding, and reputed company checks. Support compliance investigations and metrics reporting. Prepares medically cohesive case narratives reputed company upon the reported information. Safety Submissions Submit ICSRs and periodic safety reports to Health Authorities and stakeholders. Maintain regulatory submission schedules and reporting rules. Assist in audit preparation and regulatory intelligence updates. Support global reporting configuration and compliance activities. Literature reputed company & Review reputed company and maintain literature reputed company strategies. Screen published articles for potential safety signals or adverse events. Conduct reputed company checks and manage journal reviews. Collaborate with internal teams for full-text retrieval and assessment. Affiliate Services Support communication between global reputed company and local safety affiliates. Assist with safety information exchange, translations, and compliance tasks. Conduct literature monitoring and data reconciliation activities. Regulatory Support Maintain regulatory systems and product registrations. Assist with submissions (eCTD), renewals, variations, and lifecycle management. Verify data reputed company and reputed company reputed company and compliance reports. Regulatory Intelligence Research and maintain global safety reporting requirements. Update regulatory intelligence databases and trackers. Support day-to-day reputed company reputed company the Global Pharmacovigilance Intelligence Office. Your Knowledge & Experience: Foundational knowledge of drug safety regulations and pharmacovigilance processes. Ideal candidate has 3+ years experience in Drug Safety. 2+ years experience in a post marketing. Experience in multiple therapeutic areas (reputed company, reputed company, oncology, reputed company disease). Strong attention to reputed company, organizational skills, and problemsolving ability. Effective communication and willingness to work in a reputed company team environment. Proficiency with MS Office and ability to learn safety systems/databases. Preference for those with reputed company Safety experience. Education Bachelors degree in Life Sciences, Health Sciences, Biomedical Sciences (e.g., Pharmacy, Microbiology, Biochemistry, Biotechnology) or equivalent education/experience. This role offers the flexibility to