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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!

  • Patient Safety Specialist
    Function Input to high-quality and timely responses to safety queriesEnsure completion of basic training in case handling. Undergo additional training as required, such as writing a full narrative and PSUR comment.Ensure sign off in A, B and non-expeditable c (C-EU, C-KUR/DME) cases prior to processing expeditable C casesEnsure sign off on expeditable C cases (C-SSAR, C-SUSAR)Ensure compliance with global and local procedural documents and local implementation of the client and TCS, policies, processes and proceduresEnter initial and follow-up information for individual adverse event case reports of higher business value onto the global Patient Safety database, using data interpretation, coding and…
    REFERENCE NUMBER: #169
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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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  • Regulatory Publishing Specialist
    Introduction Report 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. (more…)
    REFERENCE NUMBER: #661
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  • Pharmacovigilance Team Leader with Italian
    Introduction Enter reports of drug side-effects from post-marketed or clinical study source to the safety database. Handle non-serious and serious cases according to regulatory requirements, process instructions and standard operational procedures. Resolve queries related to pharmacovigilance activities and individual case reports. (more…)
    REFERENCE NUMBER: #1048
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  • Medical Safety Specialist
    Introduction You will drive reports of drug side-effects from post-marketed or clinical study source to the safety database. Handle non-serious and serious cases according to regulatory requirements, process instructions and standard operational procedures. Resolve queries related to pharmacovigilance activities and individual case reports. (more…)
    REFERENCE NUMBER: #925
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  • Danish Speaker – Customer Response Executive
    Introduction We are looking for Danish speaking candidates who will work on animal healthcare service desk support. (more…)
    REFERENCE NUMBER: #767
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  • Case Processor
    Introduction As a Case Processor you will be responsible for entry and the evaluation and assessment of case reports for seriousness, global listedness and causality of all serious and non-serious adverse events. (more…)
    REFERENCE NUMBER: #537
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