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Life Science

Life
Science

At TCS in the Life Sciences and Health Care area we deal with pharmacovigilance and publishing activities for global pharmaceutical companies, TCS` customers. We serve patient safety with the core purpose to add value to our client’s products and safeguard the success of the business by focusing on protection of patients. We ensure that all relevant information concerning the safety of the client’s products is collected, evaluated and communicated. Our teams ensure timely and efficient reporting of adverse events and other information from pertinent to the safety profile of products towards regulatory authorities around the world as well it is essential that we comply with current regulations and guidelines. We are involved in publishing activities that is mostly connected to regulatory part of the pharmaceutical industry – but also makes sure that our customers` drugs can be used safely all over the word. Our team takes active and important parts in our clients’ everyday life and production – the business results show that they trust our knowledge and expertise.

 

Search for our job opportunities below and choose your own path!

  • Case Evaluator
    Function - Evaluation of SAE cases following the L2 path (all serious, legal, interventional studies, pregnancies) in accordance with regulatory requirements for AE reporting.- Determination of seriousness, drug product association and global labeling status (expected vs. unexpected) in order to assign the appropriate case reporting status for global distribution of regulatory case reports.- Addition of PSUR comments to individual case safety reports to facilitate PSUR authoring.- Execution of a high-quality, accurate and timely SAE case evaluation process within a therapeutic area and contribution to continuous improvement of PV system and processes.- Confirmation of the accuracy of medical coding of all…
    REFERENCE NUMBER: #786
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  • Case Processor
    Introduction (more…)
    REFERENCE NUMBER: #998
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  • Medical Advisor
    Introduction We are looking for medical doctors who are interested to work in pharmacovigilance.Experiences professionals and fresh graduates are also welcome! (more…)
    REFERENCE NUMBER: #476
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  • Publishing Specialist
    Introduction Publishing Associate will support authors to publish submission ready documents by applying appropriate compliance check to the type of document, publishing the document & also performing the QA check for the published document. Will also be responsible for renewal and continuation of marketing licenses of the drug, Coordination with multiple stakeholders to report adverse events. (more…)
    REFERENCE NUMBER: #661
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  • Senior Publishing Specialist
    Function 1. Primary Responsibilities Support and provide coordination, compilation and publishing expertise in the preparation of new and existing regulatory applications including initial applications (CTAs, MAAs etc.), amendments, supplements, variations and other submissions in compliance with health authority regulationsPrimary focus is on regulatory submissions of moderate to high complexity both eCTD and non-eCTD format, including all Modules accountability for large submissions without supervisionRegularly represent PDRO at RAFT by providing regulatory and technical input and contributing in project planning; Update PDRO on changes of strategies, timelines and risk assessment 2. Submission coordination and publishing tasks Lead and coordinate the compilation of…
    REFERENCE NUMBER: #980
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  • Drug Safety Physician
    Introduction Medical Review of a single ICSR along with Quality review and Support to EV Screening & Clinical Trial Protocol related activities (more…)
    REFERENCE NUMBER: #1069
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  • Drug Safety Scientist
    Introduction Quality review of a single ICSR along with Data Entry support, Submission review, Reconciliiation activities and Support to EV Screening & Clinical Trial Protocol related activities. (more…)
    REFERENCE NUMBER: #1067
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  • Drug Safety Associate
    Introduction Case Analysis & Data Entry along with Mailbox-handling & Submission activities. (more…)
    REFERENCE NUMBER: #1066
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  • Patient Safety Administrator
    Introduction You will enter reports of drug side-effects from post-marketed or clinical study source to the safety database, and resolve queries related to pharmacy activities and individual case reports. (more…)
    REFERENCE NUMBER: #168
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