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Real-World Data Analytics Scientist

Employer
GSK
Location
Collegeville, Pennsylvania; Waltham, Massachusetts; Research Triangle Park, North Carolina; Philadelphia, Pennsylvania
Salary
Competitive
Closing date
May 22, 2022

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Discipline
Physical Sciences, Chemistry, Information Technology
Job Type
Staff Scientist
Organization Type
Pharma
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Site Name: USA - Pennsylvania - Upper Providence, UK - London - Brentford, USA - Massachusetts - Waltham, USA - North Carolina - Research Triangle Park, USA - Pennsylvania - Philadelphia Posted Date: May 2 2022 Our Company GlaxoSmithKline (GSK) is a science-led, global healthcare company, employing over 100,000 people in more than 115 countries. Our mission is to improve the quality of human life by enabling people to do more, feel better, live longer. PURPOSE The Real-World Analytics (RWA) team applies data and methodological expertise to the analysis of existing complex health data sets. The RWA Scientist partners with the GSK global Value Evidence and Epidemiology teams to develop scientifically credible, high-quality evidence aligned with the needs of regulators, the scientific community, and decision makers responsible for granting access and reimbursement. SPECIFIC RESPONSIBILITIES As an RWA Scientist, you will use your real-world data and methodological expertise to develop design and statistical analysis plans (SAPs) for the analysis of existing complex health data sets, such as insurance claims, electronic health records, and health registries. You will work in collaboration with matrix teams, including other Scientists within the Value Evidence and Outcomes (VEO) organization, who work to translate evidence needs into a robust program of studies that support appropriate access to and evidence for GSK medicines. Design and Analysis Manage a portfolio of work to ensure delivery of quality work products to agreed timelines Share real-world data (RWD) and methodological expertise with teams to inform study planning, development, and delivery Lead the development and delivery of analysis of existing complex health data sets. Responsibilities include: author protocol and/or statistical analysis plan, write programming code to conduct statistical analysis, critically review approach and results on an ongoing basis considering design assumptions and knowledge of the data, summarize analytic findings (including limitations) in oral or written form Author specifications for analytic data sets for all RWA activities (rapid data queries (RDQ), retrospective observational studies, and other studies) to ensure appropriate interpretation and implementation of analytic design, in collaboration with RW Data Management and Programming (RWDMP). Review resulting deliverable(s) for accuracy/completeness Ensure documentation is appropriate regarding data manipulation, statistical analysis, reporting Author, maintain, finalize, and archive project delivery documentation for in-sourced studies in accordance with SOPs where appropriate Perform quality control (QC) of work products from other colleagues Provide RWD and methodological expertise to support study teams in out-sourced studies Communication of Results Co-author and bring statistical/methodological expertise in scientific publications of the in- or out-sourced RWD studies/analyses Effectively present research results to study team and other collaborators, including results interpretation and drawing appropriate inferences based on study design/statistical methods as well as assessment of study limitations Therapy Area Knowledge Understand therapy area (TA)/asset in order to apply appropriate tools (e.g., variable definitions, code lists) and use appropriate data sources Leadership and Teamwork Maintain currency with methods for the use of existing complex health datasets for research Develop in depth knowledge on the assigned asset and act as an RWA consultant within broader VEO team Apply innovative, fit-for-purpose methodology and approaches to solve critical problems Merge scientific thinking and business knowledge to identify issues, evaluate options, and implement solutions Proactively influence team members regarding appropriate research/statistical design and analytics delivery through various engagement forums: At the Value Evidence Team (VET), as part of a study team (in-sourced or out-sourced), and in coordination with the RWDMP team Mentor team members, including other RWA scientists and RW Programmers Why You? BASIC QUALIFICIATIONS We are looking for professionals with these required skills to achieve our goals: MS in a quantitative discipline such as epidemiology, health economics, health services research, health informatics, or biostatistics Three or more years experience working with RWD for use in pharmacoepidemiology and/or health outcomes research with good practical knowledge of biostatistics applied to clinical/epidemiological research Three or more years experience and practical knowledge of statistical/analytic software (e.g., SAS, R, IHD) Three or more years of experience working with RWD for use in pharmacoepidemiology research with good practical knowledge in biostatistics applied to clinical/epidemiological research Three or more years of experience delivering robust, timely, high-quality analytics Three or more years of experience collaborating and working on a wide range of projects and requests across multiple TAs PREFERRED QUALIFICATIONS If you have the following characteristics, it would be a plus: A good understanding of drug development processes and strategies, with proven ability to apply innovative statistical thinking to meet project and/or business objectives PhD degree in a quantitative discipline such as epidemiology, health economics, health services research, health informatics, or biostatistics Prior experience working in oncology within the pharmaceutical/biotech industry (preferably in real-world evidence, epidemiology, or health outcomes functional areas) 5+ years of experience working with RWD for use in pharmacoepidemiology research with good practical knowledge in biostatistics applied to clinical/epidemiological research Excellent problem-solving and analytical skills and enjoy finding efficient and innovative solutions to challenging problems Self-reliant with the ability to deliver robust, timely, high-quality analytics Fluent in written and spoken English with the ability to effectively communicate and able to articulate complex concepts to diverse audiences, demonstrated throughout the interview process. Why GSK? At GSK, we have already delivered unprecedented change over the past four years, improving R&D, becoming a leader in Consumer Health, strengthening our leadership, and transforming our commercial execution. Now, we're making the biggest 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. *LI-GSK If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US). GSK is an Equal Opportunity Employer and, in the US, we adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class. At GSK, the health and safety of our employees are of paramount importance. As a science-led healthcare company on a mission to get ahead of disease together, we believe that supporting vaccination against COVID-19 is the single best thing we can do in the US to ensure the health and safety of our employees, complementary workers, workplaces, customers, consumers, communities, and the patients we serve. GSK has made the decision to require all US employees to be fully vaccinated against COVID-19, where allowed by state or local law and where vaccine supply is readily available. The only exceptions to this requirement are employees who are approved for an accommodation for religious, medical or disability-related reasons. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit GSK's Transparency Reporting For the Record site.
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