Associate Clinical Information Analyst (on-site)
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About this role
JOB DESCRIPTION:
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to:
- Career development with an international company where you can grow the career you dream of.
- Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
- An excellent retirement savings plan with high employer contribution
- Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.
- A company recognized as a great place to work in dozens of countries around the world and named
- one of the most admired companies in the world by Fortune.
- A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.
For years, Abbott’s medical device businesses have offered technologies that are faster, more effective, and less invasive. Whether it’s glucose monitoring system, innovative therapies for treating heart disease, or products that help people with chronic pain or movement disorders, our medical device technologies are designed to help people live their lives better and healthier. Every day, our technologies help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine fingersticks.
The Opportunity
Our location in Maple Grove, MN currently has an on-site opportunity for an Associate Clinical Information Analyst. The Associate Clinical Information Analyst is responsible for supporting the development and optimization of reporting solutions which support and advance data-driven problem solving in the conduct of clinical trials. This individual will work under Good Clinical Practices, Good Clinical Data Management Practices, and other FDA regulations and guidelines, and must demonstrate solid oral and written communication skills and analytical/problem-solving skills at various levels of the organization.
What You’ll Work On
- Participate in discussions with shared service functions such as Site Management, Study Management, Data Review, Safety, etc. to gather operational, analytical, and study-specific reporting requirements.
- Support the development of elegant and efficient reporting solutions (primarily SQL queries in Oracle RDBMS and Power BI visualizations) to meet reporting requirements.
- Support ongoing maintenance and enhancement of reporting portfolio.
- Peer Review and QC of products.
- Support and train end-users of reporting portfolio.
- Support the development and standardization of reporting conventions.
Required Qualifications
- Bachelor’s degree in Computer Science, Health Sciences or related field or an equivalent combination of education and work experience
- Organizational and basic project management skills, as well as attention to detail.
- Highly skilled with Microsoft office products including Word, Excel, and Access.
- Basic ability to work with database management systems.
- Basic knowledge of database terminology and technology.
- Basic knowledge and experience in supporting the building of clinical trial databases using Oracle Clinical or equivalent.
- Basic knowledge and experience building/customizing Clinical Trial Management Software Applications.
- Ability to work in a highly matrixed and geographically diverse business environment.
- Basic ability to work within a team and as an individual contributor in a fast-paced, changing environment.
- Strong oral and written communication skills.
- Ability to meet deadlines and handle multiple assignments in a timely manner and meet assigned deadlines.
- Basic understanding of human physiology or any prior involvement with medical field.
Preferred Qualifications
- Experience in Agile Development
- Working knowledge in Data Science, Statistics, data visualization tools (e.g., PowerBI, Tableau, etc.)
- Experience with SQL, Python, Vega/Vega-Lite
Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott, and on Twitter @AbbottNews.
The base pay for this position is
$50,700.00 – $101,300.00In specific locations, the pay range may vary from the range posted.
JOB FAMILY:
Clinical Affairs / Statistics
DIVISION:
MD Medical Devices
LOCATION:
United States > Maple Grove : 6820 Wedgwood Road N.
ADDITIONAL LOCATIONS:
United States > Santa Clara : Building A - SC
WORK SHIFT:
Standard
TRAVEL:
Yes, 5 % of the Time
MEDICAL SURVEILLANCE:
No
SIGNIFICANT WORK ACTIVITIES:
Awkward/forceful/repetitive (arms above shoulder, bent wrists), Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf
EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf
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