Senior Director, Global Real-world Evidence
Il y a 3 mois
**Site Name**: UK - London - New Oxford Street, Belgium-Wavre, USA - Pennsylvania - Upper Providence
**Posted Date**: Sep 23 2024
**Senior Director, Global Real-World Evidence & Health Outcomes Research Lead - Belimumab**:
For drugs to be successful, there must be robust health outcomes data to support launch optimization, reimbursement and maintain market position. Specifically, evidence must be maintained throughout the product lifecycle as standard of care changes, new competitors are introduced, and patents expire on existing competitors. The landscape is evolving quickly as trials demonstrating efficacy in an area of unmet need may receive expedited review, or orphan product status designation which affects both GSK and competitors launch timelines and approval requirements. More and more of our customers are developing sophisticated internal health outcomes capabilities and access to real world data that can be used to better understand unmet needs and real-world effectiveness of our medicines. We need to better understand how our customers define value and to effectively collaborate with them to ensure we are generating value evidence data that includes real world evidence and cost effectiveness analysis that is impactful for payers, health systems, providers, and patients.
The role of Senior Director, Global Real-World Evidence & Health Outcomes Research Lead is critical to achieving this ambition by ensuring that each medicine GSK brings to market is supported by scientifically credible, high-quality evidence that drives competitiveness and strong evidence-based product positioning, value propositions and value-based pricing. The role is essential for the alignment of evidence with the requirements of customers responsible for marketing authorization, recommendation and reimbursement leading to successful patient access, product use and commercial success.
Within this organisation as the VP, Head of Global Real-World Evidence & Health Outcomes Research, Sulabha Ramachandran will be leading a team which incorporates the legacy VEO/Non-Interventional Studies capabilities teams under a newly evolved name that more closely reflects their purpose and the research they deliver.
**Key Responsibilities include, but are not limited to**:
The role will serve as single point accountable lead for a complex priority asset and lead a team of high performing scientists with expertise in real-world evidence and other non-interventional study methods. The role will be a key member of the Global Real-World Evidence & Health Outcomes Research Lead Therapy Area LT and other relevant matrix leadership teams. The Senior Director, Global Real-World Evidence & Health Outcomes Research Lead will be accountable for ensuring team members engage closely with medical and matrix stakeholders and partner effectively in data generation plan (DGP) planning, design, execution, translation, and dissemination for the asset.
- Provide leadership, management, and development of the asset team, including recruitment and capability building, support, and development opportunities through best practice sharing to create high performing, quality assured resources which support the business.
- Partner effectively with matrix stakeholders in planning and design of the DGP for the asset, drive disciplined execution of studies and activities, translate results, and disseminate data and research findings to all relevant internal and external stakeholders.
- Provide guidance for best practice in real world evidence/ NIS methodologies, including enabling external scientific advice, ensuring appropriate protocol review committee’s advice sought and incorporated.
- Drive innovation and inform ideas and options through effective engagement with external experts, clinical guideline groups, HTA agencies, methodology and policy forums, and by leveraging knowledge of the external policy and decision maker environment to enable more efficient evidence development for the asset across the lifecycle (e.g. discovery, launching and life cycle management assets)
- Integrate excellent understanding of the evolving global NITAG, Health Technology Assessment, clinical guidelines groups, policy decision makers and payer environment, including recommendation, reimbursement, pricing, and access in relevant therapy area.
- Negotiate with key stakeholders as to what evidence for the asset is and is not developed, weighing risks and benefits to optimize reimbursement opportunities, support scientific exchange and clinical guideline development.
- Deliver the materials to inform internal governance decision making (e.g. Medical Review Board, etc)
- Facilitate alignment and partnership to enable more effective interactions within the complex stakeholder matrix, e.g. clinical, commercial, market access, medical affairs functions, priority market LOCs as well as external third-party suppliers.
- Represent GSK in external collaborations, engagement and scientific evi
-
Senior Director, Global Real-world Evidence
Il y a 3 mois
Wavre, Belgique GSK Temps plein**Site Name**: UK - London - New Oxford Street, Belgium-Wavre, USA - Pennsylvania - Upper Providence **Posted Date**: Sep 23 2024 **Senior Director, Global Real-World Evidence & Health Outcomes Research Lead - RSV**: For drugs to be successful, there must be robust health outcomes data to support launch optimization, reimbursement and maintain market...
-
Senior Director, Global Real-world Evidence
Il y a 3 mois
Wavre, Belgique GSK Temps plein**Site Name**: UK - London - New Oxford Street, Belgium-Wavre, USA - Pennsylvania - Upper Providence **Posted Date**: Sep 23 2024 **Senior Director, Global Real-World Evidence & Health Outcomes Research Lead - Herpes zoster**: For drugs to be successful, there must be robust health outcomes data to support launch optimization, reimbursement and maintain...
-
Senior Director, Global Real-world Evidence
Il y a 3 mois
Wavre, Belgique GSK Temps plein**Site Name**: UK - London - New Oxford Street, Belgium-Wavre, USA - Pennsylvania - Upper Providence **Posted Date**: Sep 23 2024 **Senior Director, Global Real-World Evidence & Health Outcomes Research Lead - Pneumococcal MAPS**: For drugs to be successful, there must be robust health outcomes data to support launch optimization, reimbursement and maintain...
-
Senior Director, Global Real-world Evidence
Il y a 3 mois
Wavre, Belgique GSK Temps plein**Site Name**: UK - London - New Oxford Street, Belgium-Wavre, USA - Pennsylvania - Upper Providence **Posted Date**: Sep 23 2024 End date job posting: 7th October 2024 **_ Chief Patient Organisation_** - The Chief Patient Organisation led by the Chief Patient Officer is accountable for bringing external perspectives of thought leaders, academic...
-
Director, Global Real-world Evidence
Il y a 2 mois
Wavre, Belgique GSK Temps plein**Site Name**: USA - Pennsylvania - Upper Providence, Belgium-Wavre, UK - London - New Oxford Street **Posted Date**: Oct 10 2024 For drugs to be successful, there must be robust health outcomes data to support launch optimization, reimbursement and maintain market position. Specifically, evidence must be maintained throughout the product lifecycle as...
-
Director, Global Real-world Evidence
Il y a 3 mois
Wavre, Belgique GSK Temps plein**Site Name**: UK - London - New Oxford Street, Belgium-Wavre, USA - Pennsylvania - Upper Providence **Posted Date**: Sep 23 2024 End date job posting: 7th October 2024 **_ Chief Patient Organisation_** - The Chief Patient Organisation led by the Chief Patient Officer is accountable for bringing external perspectives of thought leaders, academic...
-
Associate Director, Global Real-world Evidence
Il y a 2 mois
Wavre, Belgique GSK Temps plein**Site Name**: USA - Pennsylvania - Upper Providence, Belgium-Wavre, Cambridge MA, UK - London - New Oxford Street, USA - Maryland - Rockville **Posted Date**: Oct 8 2024 Established as a focused global function**, Data Generation & Scientific Communications**, is uniquely placed to help accelerate the successful integration of our medicines and vaccines...
-
Real-world Evidence and Publication Manager
Il y a 6 mois
Wavre, Belgique AbbVie Temps plein**Company Description** **Job Description** Job purpose and objectives**: You will be responsible for driving and executing our evidence generation plans within assigned therapeutic area - and for keeping oversight of evidence generation activities and publications across these therapeutic domains. You will have the opportunity to contribute to impacting and...
-
Associate Director, Real-World Analytics
Il y a 6 mois
Wavre, Belgique 1925 GlaxoSmithKline LLC Temps pleinThe Real-World Analytics (RWA) Scientist, uses data and methodological expertise to develop study designs and statistical analysis plans (SAPs) for the analysis of existing complex health data sets, including real-world data (RWD). This work is conducted in collaboration with Scientists in the Epidemiology and Medical Evidence Generation organizations, and...
-
Ta Head
Il y a 3 mois
Wavre, Belgique GSK Temps plein**Site Name**: USA - Pennsylvania - Upper Providence, Belgium-Wavre, UK - London - New Oxford Street **Posted Date**: Sep 23 2024 GlaxoSmithKline (GSK) is a global healthcare company committed to improving the quality of human life by enabling people to do more, feel better, and live longer. We discover, develop, and deliver innovative medicines, vaccines,...
-
Senior Director Quality
Il y a 3 mois
Wavre, Belgique GSK Temps plein**Site Name**: UK - London - New Oxford Street, Belgium-Wavre, Italy - Siena, Spain - Madrid **Posted Date**: Sep 1 2024 **Senior Director, Quality & Risk Management, Global Health**: **The deadline for the job posting is the 15th of September**: **Background**: Global Health (GH) is a cornerstone of GSK’s ESG agenda, committed to change the trajectory of...
-
Serm Senior Scientific Director, Oncology
il y a 4 semaines
Wavre, Belgique GSK Temps plein**Site Name**: UK - London - Brentford, Belgium-Wavre **Posted Date**: Nov 15 2024 **Job Purpose**: Responsible to lead medical and scientific staff within the SERM (Safety Evaluation & Risk Management) and defining and driving the strategy and vision of clinical safety and pharmacovigilance activities in alignment with Global Safety business...
-
Senior Director, Global Content Creation Oncology
Il y a 2 mois
Wavre, Belgique GSK Temps plein**Site Name**: USA - Pennsylvania - Upper Providence, Belgium-Wavre, Cambridge MA, Philadelphia Walnut Street, UK - London - New Oxford Street, USA - North Carolina - Durham **Posted Date**: Oct 4 2024 The purpose of the **Senior Director, Global Content Creation Oncology r**ole is to develop, maintain and oversee the development and delivery of the Global...
-
Senior Director, Global Medical Education
Il y a 2 mois
Wavre, Belgique GSK Temps plein**Site Name**: USA - Pennsylvania - Upper Providence, Belgium-Wavre, Cambridge MA, Philadelphia Walnut Street, UK - London - New Oxford Street, USA - Massachusetts - Waltham, USA - North Carolina - Durham **Posted Date**: Oct 4 2024 The** **Senior Director, Global Medical Education & Customer Experience Delivery** will work above Therapeutic Areas and...
-
Global Sterility Assurance Director
il y a 3 semaines
Wavre, Belgique GSK Temps plein**Site Name**: UK - County Durham - Barnard Castle, Belgium-Wavre, Upper Merion, USA - Maryland - Rockville, Ware **Posted Date**: Nov 21 2024 The Global Sterility Assurance Director at GlaxoSmithKline (GSK) is a pivotal role within the Strategic Product Quality staff, bringing critical expertise in sterility assurance across various initiatives and...
-
Senior Manager, Procurement
Il y a 3 mois
Wavre, Belgique GSK Temps plein**Site Name**: Belgium-Wavre **Posted Date**: Sep 12 2024 Job Purpose As the **Senior Manager, Head of Procurement **you will be at the forefront of driving GSK’s purpose to **unite science**, **technology**, and **talent** to get **ahead of disease** together. You will do so by partnering with Indirect spend owners across all GSK business lines, and...
-
Director, Global Regulatory Affairs
Il y a 2 mois
Wavre, Belgique GSK Temps plein**Site Name**: Wavre, GSK HQ, Stevenage **Posted Date**: Oct 1 2024 **Job Purpose** Ensure the development of appropriate regional regulatory strategy(s) and their execution for assigned asset(s) consistent with Medicines Development Strategy. This goal has to be achieved both as a component of an overall global regulatory approach and ensure compliance...
-
Global Clinical Development Associate Director
Il y a 3 mois
Wavre, Belgique GSK Temps plein**Site Name**: UK - London - New Oxford Street, Belgium-Wavre, Canada - Ontario - Mississauga, UK - Hertfordshire - Stevenage, USA - Massachusetts - Waltham, USA - Pennsylvania - Upper Providence, Warsaw **Posted Date**: Sep 23 2024 We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive...
-
Statistics Director
Il y a 4 mois
Wavre, Belgique GSK Temps plein**Site Name**: UK - London - New Oxford Street, Amsterdam, Collegeville TSA, Rockville Biopharm, Siena, Stevenage, Waltham, Wavre **Posted Date**: Aug 29 2024 At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. R&D is committed to discovering and delivering transformational...
-
Senior Director, Bioethics, R&d Bioethics
Il y a 3 mois
Wavre, Belgique GSK Temps plein**Site Name**: USA - Pennsylvania - Upper Providence, Belgium-Wavre, GSK HQ, RTP **Posted Date**: Sep 19 2024 **Job Purpose**: The role of Senior Director, Bioethics, R&D Bioethics and Policy, provides internal and external **strategic thought leadership on the development of Bioethics positions and recommendations for areas impacting R&D strategy and...
