Hours: Part-time (up to 20 hours per week)
Location: Chelsea, London
Company Overview:
The Thrombosis Research Institute is a renowned institution dedicated to advancing research in the field of thrombosis and cardiovascular health outcomes. The institute has been involved in laboratory studies, randomised clinical trials and large international observational registries. The institute is now moving into the area of large national and regional databases, as well as studies that use administrative claims, laboratory results, EHR data, and large-scale biomedical databases like UK Biobank. For further information on the scope of our research, please visit: https://www.tri-london.ac.uk/.
The Thrombosis Research Institute is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, or any other characteristic protected by law. We encourage candidates from all backgrounds to apply.
Role Overview:
You will ensure TRI studies are planned and implemented to the highest standards, in compliance with ICH-GCP guidelines, TRI SOPs, and all applicable regulatory guidelines. Develop, modify, and maintain computer programs required to enhance clinical care and research; analyze research needs to determine feasibility of adapting manual procedures to computer applications.
Key Responsibilities:
1. Specify, develop, modify, maintain and validate computer programs
2. Specify and develop programs to support research needs
3. Validate computer applications
4. Analyze manual processes to convert to computer applications
5. Select software for statistical analysis environment
6. Help design database through CRF and database design review
7. Design project directory architecture
8. Select electronic file transfer technologies
9. Prepare and maintain project documentation
10. Follow SOP documentation standards
11. Maintain analysis programming notebook
12. Estimate and manage project workload
13. Provide status updates to supervisor
14. Estimate time required to complete various tasks
15. Attend and contribute to team meetings as required
16. Coordinate statistical programming efforts of others on project
17. Learn, apply and share new techniques to increase efficiencies
18. Become an advanced SAS programmer
19. Understand industry trends (regulatory, technical)
20. Assist in mentoring junior staff as needed
21. Educate others in formal and informal settings
22. Answer analysis programming questions that others may have
23. Perform other related duties incidental to the work described herein
Desired Skills and Experience:
1. A Bachelor’s degree in mathematics or a computer-related field, or equivalent coursework or technical training
2. Two years of programming or analytical experience with knowledge of the SAS computer language and systems. Preferred experience includes previous clinical trials experience, proficiency with SAS software, and exposure to the UNIX operating system
3. Good SAS programming skills with knowledge in SAS/Macro, SAS Proc reports, and ODS
4. Good working knowledge in SAS/Graph and Proc SQL
5. Knowledge of R programming language would be an advantage
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