Job title: Technical Associate

Company: GlaxoSmithKline

Job description: Job Description : Standort: Bengaluru Luxor North Tower Datum: Jun 16 2022 Ready to help shape the future of healthcare? At GSK, we have already delivered unprecedented change over the past four years, improving R&D, becoming a leader in Consumer He

Job Description : Standort: Bengaluru Luxor North Tower Datum: Jun 16 2022 Ready to help shape the future of healthcare At GSK, we have already delivered unprecedented change over the past four years, improving R&D, becoming a leader in Consumer Healthcare, strengthening our leadership, and transforming our commercial execution. Now, we’re making the most significant changes we’ve made to our business in over 20 years. We’re on track to separate and create two new companies in 2022: New GSK with a leading portfolio of vaccines and specialty medicines as well as R&D based on immune system and genetics science and a new world-leading consumer healthcare company of loved and trusted brands. With new ambition comes new purpose. For New GSK, this is to unite science, talent, and technology to get ahead of disease together – all with the clear ambition of delivering human health impact stronger and more sustainable shareholder returns and as a new GSK where outstanding people thrive. Getting ahead means preventing disease as well as treating it. How we do all this is through our people and our culture. A culture that is ambitious for patients – so we deliver what matters better and faster accountable for impact – with clear ownership of goals and support to succeed and where we do the right thing. So, if you’re ready to improve the lives of billions, join us at this exciting moment in our journey. Join our challenge to get Ahead Together. The post holder provides cross enterprise technical support within PV Excellence (PVE) and the business, as required.. The post holder supports Global Process Owners(GPOs), Safety Process Leads (SPLs) and the business, by undertaking identified operational tasks. Key Responsibilities/Activities (dependent on areas supported by each TA) Assist GPOs/SPLs to provide strategic oversight for enterprise PV processes. Assist GPOs/SPLs to deliver innovative, efficient, holistic, end-to-end safety processes that are compliant with global PV regulations and reflect enterprise business needs, including Process Simplification. Assist the Global Safety Quality Team with issues management, including entry of records into central systems, follow-up on response plans, and generation of quality metrics Assist record owners with records management and archiving tasks Provide operational, technical and maintenance support of appropriate PVE Workstreams Undertake Template Manager Role to support for PV documentation in VeeVa Vault (Regulatory and Clinical) Support interaction between PVE and 3rd Party Vendor Activities for Aggregate Report management Provide support for metric collection, compilation and reporting Provide support for Management Monitoring Manage daily triage of group mailboxes Contribute to process improvement Undertake role of Subject Matter Expert, when required. Business owner of document management systems Review content on PVE owned webpages and ensure materials are up to date and fully operational Support Signal detection, including CVW Support Eudravigilance activities Support RMP and Targeted Safety Study (TSS)/Post Approval Safety Study (PASS) activities Support eTMF Support Medical Devices Support Case Awareness Tool/Autolistedness profile/TOI/MedDRA Support Medication Error activities Support PIER Report generation/meta data change requests Support PRION alerts and QRG maintenance Provide oversight of local Reference Safety Information updates and address queries Provide support for training, inspections, and audits Key Skills Excellent computer skills including Word, Excel, Internet/Intranet, document management systems Excellent organisational skills Demonstrates ability to work with tight deadlines under pressure, while maintaining a high level of accuracy, attention to detail and integrity Functions as a team player Demonstrates ability to effectively communicate (written and verbal) Ability to effectively handle and appropriately escalate issues based on risk in a timely manner Awareness of PV processes and global PV regulations Preferred knowledge of process improvement techniques and ability to analyze performance metrics to drive continuous improvement Preferred knowledge of other related disciplines e.g. clinical, regulatory affairs, clinical statistics relevant to aggregate report writing and clinical development Demonstrates ability to be able to work independently, in a flexible manner and adjust to change Experience Minimum high school diploma or equivalent plus 3-4 years’ experience providing technical support for a high volume medically oriented or Clinical R&D department in a large corporation. Higher education advantageous. Familiarity with medical/scientific terminology desirable. Working knowledge of R&D organisation preferred. At GSK we value diversity (Gender, LGBTQ +, PwD etc.) and treat all candidates equally. We aim to create an inclusive workplace where all employees feel engaged, supportive of one another, and know their work makes an important contribution. .LI-GSK Unser Ziel ist es, eines der innovativsten, leistungsf higsten und vertrauensw rdigsten Gesundheitsunternehmen der Welt zu werden. Wir sind davon berzeugt, dass jeder von uns einen einzigartigen Beitrag zu GSK leistet. Wenn wir unser Wissen, unsere Erfahrungen und besonderen Talente vereinen, werden wir ein unglaubliches Ergebnis erzielen. Kommen Sie zu GSK und finden Sie einen inspirierenden Arbeitsplatz, an dem Sie Ihr Bestes f r unsere Patienten und Verbraucher geben. Ein Ort, an dem Sie ganz Sie selbst sein, sich wohlf hlen und weiterentwickeln k nnen. Wichtiger Hinweis f r Arbeitsvermittlungsunternehmen/-agenturen GSK akzeptiert keine Empfehlungen von Arbeitsvermittlungsunternehmen und/oder Arbeitsvermittlungsagenturen f r die auf dieser Website ausgeschriebenen freien Stellen. Alle Arbeitsvermittlungsunternehmen/-agenturen m ssen sich an die Abteilung f r gewerbliche und allgemeine Beschaffung/Personalabteilung von GSK wenden, um die schriftliche Einwilligung einzuholen, bevor sie GSK Bewerber empfehlen. Der Erhalt einer schriftlichen Einwilligung ist Voraussetzung f r jegliche Vereinbarung (sowohl m ndlich als auch schriftlich) zwischen dem Arbeitsvermittlungsunternehmen/der Arbeitsvermittlungsagentur und GSK. Falls diese Genehmigung nicht erteilt wurde, wird davon ausgegangen, dass s mtliche Handlungen des Arbeitsvermittlungsunternehmens/der Arbeitsvermittlungsagentur ohne die Zustimmung von GSK oder ohne eine vertragliche Vereinbarung mit GSK unternommen wurden. Aus diesem Grund haftet GSK nicht f r irgendwelche Geb hren, die aus solchen Handlungen oder aus Empfehlungen von Arbeitsvermittlungsunternehmen/-agenturen f r die auf dieser Website ausgeschriebenen freien Stellen entstehen.

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Location: Bangalore, Karnataka

Job date: Sat, 18 Jun 2022 22:35:54 GMT

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