- Collegeville, PA
Site Name: USA - Pennsylvania - Upper Providence
Posted Date: Nov 18 2020
GlaxoSmithKline is one of the world's foremost pharmaceutical and healthcare companies, with statisticians and programmers working in Research and Development with a global footprint spanning the UK, US, Canada and India. The Biostatistics division includes a Clinical Programming department, covering all phases of clinical drug development and commercialisation in a wide range of therapeutic areas. Programming's deliverables form the core of all regulatory submissions, health authority assessments, safety updates and publications (for peer review journals and scientific meetings).
In recognition of the developing sophistication and technical requirements of the role, Clinical Programming was formed as a standalone department distinct to Clinical Statistics. Programming asset teams are now stepping up to achieve the goal of being the Biostatistics' leaders of delivery and execution, in a way that optimises, expedites and delivers to the highest quality. In addition to the group's activities supporting GSK's pipeline of drugs, key accountabilities include developing and implementing strategies for programming resourcing using both internal and external resource; driving CDISC implementation for the reporting of clinical trials; and identifying and implementing IT solutions to offer further benefit and efficiency for the group's activities.
The Clinical Programming team at GSK has a strong focus on innovative ways of working and we are leading the way to implement these innovations and embracing an evolution for increased data science skills; this is already resulting in the introduction of new programming languages, technology and software. Some of these initiatives include the pathway for adoption of R and Python open source coding into day to day programming tasks, exploring machine learning to drive efficiencies for clinical reporting, developing desktop visualisation capabilities and we even have an annual challenge for Programmers who are rewarded for bringing new innovations into the department. But it's not just about the tech! We also encourage involvement in other initiatives too and we focus on your personal development path, building your project and leadership skills, your inter-departmental liaison and collaboration skills and we provide you with opportunities to get closer to the science and decision making.
Within the clinical programming team Senior Programmers and Principal Programmers support, guide, or make a major contribution to the planning and execution of multiple programming activities for GSK clinical trials. They are accountable for creating, verifying, and documenting analyses of clinical data while adhering to study protocols, analysis plans and GSK / industry standards.
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
- Demonstrate strong programming expertise, with the ability to execute a wide range of programming activities with minimal supervision
- Identify gaps in current programming best practices and may offer suggestions
- Understand the management of programs, including change control and their importance
- Ensure adherence to standards and has an awareness of evolving standards, both internal and external
- Keep an awareness of departmental strategies and initiatives
- Provide input to strategic planning, where requested and under supervision, which may be shared with stakeholders
- Informs supervisor and matrix leaders of appropriate progress and activities
- Oversee the work of contractors/placement students
Why you? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals:
- BS in mathematics, statistics, computer science (or related discipline)
- 2+ years of experience with SAS and/or R programming
- Experience with programming language(s)
- Experience with oncology
- Support or validation programming experience
- Experience with writing and applying Metadata Specifications/Derivations
Preferred Qualifications: If you have the following characteristics, it would be a plus:
- Extensive working knowledge of GxP, ICH requirements, internal processes and external regulations that govern drug development (where applicable)
- Takes responsibility for oversight of others work as assigned by manager
- Demonstrated effectiveness in both oral and written communications, able to express ideas and incorporate feedback to produce a completed quality deliverable
- Able to explain technical approaches to peers and non-technical colleagues/settings
- Deliver presentations with clarity in internal forums and/or external professional industry meetings
- Experience with R and Tidyverse programming
Why GSK? Our values and expectationsare at the heart of everything we do and form an important part of our culture.
These include Patient focus, Transparency, Respect, Integrity along with Courage, Accountability, Development, and Teamwork. As GSK focuses on our values and expectations and a culture of innovation, performance, and trust, the successful candidate will demonstrate the following capabilities:
- Operating at pace and agile decision-making - using evidence and applying judgement to balance pace, rigour and risk.
- Committed to delivering high quality results, overcoming challenges, focusing on what matters, execution.
- Continuously looking for opportunities to learn, build skills and share learning.
- Sustaining energy and well-being.
- Building strong relationships and collaboration, honest and open conversations.
- Budgeting and cost-consciousness.
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.
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