Drug Safety Associate
1 day ago
Title: Drug Safety Associate Date: 5 Sept 2025 Location: Bangalore, KA, IN Job Description We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations to be future-ready. We offer accelerated, global growth opportunities for talent that’s bold, industrious, and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship and is guided by passion, innovation, collaboration, and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out Looking to jump-start your career? We understand how important the first few years of your career are, which create the foundation of your entire professional journey. At Indegene, we promise you a differentiated career experience. You will not only work at the exciting intersection of healthcare and technology but also will be mentored by some of the most brilliant minds in the industry. We are offering a global fast-track career where you can grow along with Indegene’s high-speed growth. We are purpose-driven. We enable healthcare organizations to be future ready and our customer obsession is our driving force. We ensure that our customers achieve what they truly want. We are bold in our actions, nimble in our decision-making, and industrious in the way we work.Must Have Associate - Pharmacovigilance Officer I You will be responsible for: "Confirm validity of case by identifying minimum criteria for case creation. � Perform duplicate search to create either an initial case or a follow-up case. � Understanding the principles and concepts associated with patient safety case-handling process including regulatory requirements for reporting individual case safety reports. � Identify serious adverse events and special scenario cases which includes lack of efficacy, exposure, and pregnancy case, at risk cases, and product quality complaint only cases. � Attach the relevant source documents or any safety information/queries/follow-up information that is relevant to the case. � Facilitate follow-up based on queries from Data entry/QC/MR or based on inconsistent/missing information in the source file. Responsible for coding which includes adverse event, medical history, Lab data, Indications etc using standardized terminology from a medical coding dictionary, such as MedDRA. � Code products (Suspect/co-suspect, Concomitant) as per Client conventions and Regulatory requirements. � Draft narratives." Your impact: About you: (Desired profile) Must have: Understand the principles and concepts associated with case-handling process and overall Drug Research Process. � Cognitive abilities including verbal reasoning, attention to detail, and critical and analytical thinking. � Good knowledge on therapy area/medical terminology. � Good comprehension skills. � Good communication (verbal and written), with fluency in English and interpersonal skills. Nice to have: (Additional desired qualities) Perks: (Mention if any, otherwise ignore) EQUAL OPPORTUNITY Indegene is proud to be an Equal Employment Employer and is committed to the culture of Inclusion and Diversity. We do not discriminate on the basis of race, religion, sex, colour, age, national origin, pregnancy, sexual orientation, physical ability, or any other characteristics. All employment decisions, from hiring to separation, will be based on business requirements, candidate�s merit and qualification. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics.Good to have EQUAL OPPORTUNITY Indegene is proud to be an Equal Employment Employer and is committed to the culture of Inclusion and Diversity. We do not discriminate on the basis of race, religion, sex, colour, age, national origin, pregnancy, sexual orientation, physical ability, or any other characteristics. All employment decisions, from hiring to separation, will be based on business requirements, the candidate’s merit and qualification. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics.
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Drug Safety Associate
2 weeks ago
Bengaluru, India Bitwise Solutions Full timeDrug Safety Associate Job Duties Drug safety associates responsibilities include: - Reviewing adverse event reports, safety data sheets, and physician advisories to identify potential risks associated with a particular drug - Conducting site visits to observe the distribution process to ensure compliance with federal regulations - Monitoring compliance...
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Drug Safety Associate I
2 weeks ago
Bengaluru, India Novo Nordisk Full timeDrug Safety Associate I Drug Safety Associate I Drug Safety Associate I
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Drug Safety Associate
1 week ago
Bengaluru, India Seven Consultancy Full timeJob Description - Ensure that safety reports received from investigational sites or post-marketing sectors are identified and reported in accordance with ICH-GCP standards and standard operational procedures. - Organize collected reports based on the seriousness or effectiveness of the drug. - Maintain consistency in assessing adverse reaction reports...
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Drug Safety Associate
4 days ago
Bengaluru, Karnataka, India Indegene Full time**Date**:29 Aug 2025 **Location**:Bangalore, KA, IN - Job Description- - Must Have- Associate - Pharmacovigilance Officer I You will be responsible for: "Confirm validity of case by identifying minimum criteria for case creation. - Perform duplicate search to create either an initial case or a follow-up case. - Understanding the principles and concepts...
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Drug Safety Associate
1 week ago
Bengaluru, India Merck KGaA Darmstadt Germany Full timeWork Your Magic with us! Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of...
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Drug Safety Associate
1 week ago
Bengaluru, Karnataka, India Indegene Full time**Date**:20 Sept 2025 **Location**:Bangalore, KA, IN - Job Description- - Must Have- Data Management: - Perform duplicate search as per the requirement. - Process Individual Case Safety Reports (ICSRs) from all sources in compliance with applicable regulations, and in accordance with client specific requirements and timelines. - Identify serious adverse...
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Junior Drug safety associate
1 day ago
Bengaluru, India Indegene Full timeTitle: Junior Drug safety associate Date: 2 Sept 2025 Location: Bangalore, KA, IN Job Description We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations to be future-ready. We offer accelerated, global growth opportunities for talent that’s bold, industrious, and nimble. With Indegene, you...
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Junior Drug Safety Associate
6 days ago
Bengaluru, Karnataka, India Indegene Full timeLooking to jump-start your career? We understand how important the first few years of your career are, which create the foundation of your entire professional journey. At Indegene, we promise you a differentiated career experience. You will not only work at the exciting intersection of healthcare and technology but also will be mentored by some of the most...
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Drug Safety Specialist
1 day ago
Bengaluru, India Parexel Full timeWhen our values align, there's no limit to what we can achieve. Key Accountabilities : The below responsibilities vary as per applicable as per the job role. General Maintaining a good working knowledge of the adverse event safety profile of the assigned drugs, labeling documents, client’s guidelines, and SOPs, and Global drug safety regulations...
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Bengaluru, India Seven Consultancy Full timeJOB DETAILS 1)Needs to ensure that most of the safety reports that are received from the investigational sites or from the post- marketing sector must be identified & reported in accordance to the ICH-GCP standards & also by the standard operational procedures.2)Reports that are collected must be organized based on the seriousness or effectiveness of the...