6 people are interested
6 people are interested
Do good for your community while using your professional expertise. Work with talented peers on a rewarding non-profit cause related program. Rare Genomics Institute is making a difference. Rare Genomics Institute is a non-profit organization that helps families in need of genome research.
The IT Department is responsible for supporting and maintaining the company’s IT systems and for providing support to all users. The department is also responsible for data governance security and resolving any IT-related faults quickly and efficiently, including a broad range of queries from how to set up an email account to system diagnostics, plus enhancing and developing the IT provision extended within the business.
We are seeking an IT intern to consolidate multiple Excel Files into one file for further analysis.
Complete short term project to achieve following objectives:
Phase 1: Write Python program to Cleanse, and Consolidate Multiple excel file into one excel or CSV file.
Create one or more scripts to create a Final Excel/CSV file from multiple excel files.
The script must be:
- Repeatable, so that it can be run with addition of more excel files in future.
- All logic in one place so can change with the business
- Can be handed off to others
Goal is to deliver script/code and related artifacts.
Possibility to extend the project to Phase 2 to Analyze using PowerBI to perform data analytics.
About Rare Genomics Institute
8504 Firestone Blvd., #198, Downey, CA 90241, US
At RG, we are more than just an organization. We are a community dedicated to helping rare disease patients find hope for a cure. We work alongside patients and their families, providing them with the necessary tools, knowledge, and connections so that they can better understand the cause of their disease. We believe that every patient deserves more out of life.
Rare Genomics Institute (RGI) is a nonprofit organization dedicated to helping rare disease
patients find a diagnosis, treatment, and pathway to a cure. Through personalized research
projects, RGI provides access to world leading medical institutions and scientists to conduct
genomic sequencing, coordinates with clinicians and counselors to interpret findings, and offers an
online crowd-funding platform to deliver financial solutions. RGI also supports rare disease
advocacy by fostering an online community of rare disease patients and supporting rare disease
research through a yearly grant competition.
Since being founded in 2011, RGI has completed over 300 genetic sequencing and analysis
projects, assisted patients fund over $3.5 million worth of genomic sequencing, discovered 8
unique genetic mutations in-house, given over $2 million dollars in grants to researchers on rare
disease, and developed an online community with over 10,000 rare disease members.
Through volunteers, RGI is able to slowly push science and health care forward to meet the needs
of patients affected by rare diseases. To learn more about RGI check out our website, like us on
Facebook, and follow us on Twitter!
This is a Virtual Opportunity with no fixed address.
October 12, 2021
- 5 hours per week