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From Home Clinical Database Programmer Jobs in Chicago, IL

Ametek

Database Engineer

Mount Prospect, IL · On-site

Our solutions support clinicians and patients when it matters most, and data is at the heart of ... Exposure to SSIS tool or ETL/ELT processes (development, support, migration from one tool to ...

Ametek

Database Engineer

Mount Prospect, IL

Our solutions support clinicians and patients when it matters most, and data is at the heart of ... Exposure to SSIS tool or ETL/ELT processes (development, support, migration from one tool to ...

Trova Search

Database Engineer

Oakbrook Terrace, IL · On-site

Build and manage scalable data pipelines for collecting, transforming, and processing data from ... database administration and data engineering. * Contribute to additional projects and ...

Joint Commission

Database Engineer

Villa Park, IL

$89K - $114K/yr

Design, build, and maintain robust data pipelines to ingest, process, and transform data from ... and best practices in database and data engineering. * Perform additional duties and ...

Joint Commission

Database Engineer

Villa Park, IL · On-site

$89K - $114K/yr

Design, build, and maintain robust data pipelines to ingest, process, and transform data from ... and best practices in database and data engineering. * Perform additional duties and ...

Ardmore Roderick

Database Developer-2506270RV14

Chicago, IL · On-site

$124K - $154K/yr

As a Database Developer , you join a team of infrastructure solutions experts working to solve our ... Participate in all stages of the development life cycle, from concept planning to build, testing ...

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All JobsClinical Database Programmer JobsFrom Home Clinical Database Programmer JobsFrom Home Clinical Database Programmer Jobs in Chicago, IL

From Home Clinical Database Programmer information

See Chicago, IL salary details

$71.6K

$122.5K

$218.4K

How much do from home clinical database programmer jobs pay per year?

As of Sep 1, 2026, the average yearly pay for from home clinical database programmer in Chicago, IL is $122,548.00, according to ZipRecruiter salary data. Most workers in this role earn between $82,400.00 and $185,400.00 per year, depending on experience, location, and employer.

What is the difference between From Home Clinical Database Programmer vs On-Site Clinical Data Coordinator?

AspectFrom Home Clinical Database ProgrammerOn-Site Clinical Data Coordinator
CredentialsTypically requires a degree in health informatics, computer science, or related field; certifications like CDMP or SAS are commonUsually holds a degree in health sciences, nursing, or related field; certifications like CDMP may be preferred
Work EnvironmentRemote, home-based setting with flexible hoursOn-site at clinical trial sites or healthcare facilities
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, clinical research organizations, healthcare providers

While both roles involve managing clinical data, the From Home Clinical Database Programmer works remotely focusing on database development and programming, whereas the On-Site Clinical Data Coordinator handles data collection and management directly at clinical sites. The choice depends on your preference for remote work versus on-site responsibilities.

What are the most commonly searched types of Clinical Database Programmer jobs in Chicago, IL?

The most popular types of Clinical Database Programmer jobs in Chicago, IL are:

What are popular job titles related to From Home Clinical Database Programmer jobs in Chicago, IL?

For From Home Clinical Database Programmer jobs in Chicago, IL, the most frequently searched job titles are:

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The top searched job categories for From Home Clinical Database Programmer jobs in Chicago, IL are:

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Cities near Chicago, IL with the most From Home Clinical Database Programmer job openings:

From Home Clinical Database Programmer jobs near you

Clinical Data Manager

ProPharma Group

Western Springs, IL • On-site

Full-time

Posted 19 days ago

Job description

For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners' most high-profile drug and device programs.
Clinical Data Manager
The Clinical Data Manager performs activities pertaining to the conduct of Phase I-III clinical trials in accordance with ICH/Good Clinical Practices (GCP) and other relevant procedures and guidelines. The CDM ensures, from a data management perspective, assigned trials on time, within budget, and with highest achievable quality.
Summary of the Essential Functions of the Job
  • Participate as the primary data management representative on Incyte multidisciplinary project teams and ensure effective communication exchange.
  • Responsible for communicating key clinical data management metrics (e.g., data entry status, query resolution and a1ging, etc.) and determining appropriate actions in conjunction with study team.
  • Responsible for the review, development and/or writing of clinical trial documents and manuals, including but not limited to Case Report Forms, Edit Checks, Data Management Plans, Clinical Data Review Plans and eCRF Completion Guidelines.
  • Participate in User Acceptance Testing (UAT), as needed.
  • Participate in Quality Control (QC), as needed.
  • Responsible for working with the assigned Clinical Database Programmer(s) to ensure the development of the Data Flow Chart(s), Data Transfer Specifications and Import Guidelines.
  • Assist with site and/or third party vendor training on CDM-related topics.
  • Responsible for providing data review training and guidance to Sr. Clinical Data Coordinators that are supporting their trial(s).
  • Perform data review and discrepancy resolution, as needed.
  • Responsible for archiving trial(s) and associated documentation upon trial(s) completion.
  • Ensure adherence to Good Clinical Practice and all applicable local and international regulations.

Minimum Requirements
  • Minimum of 5 years of data management experience is required.
  • Bachelor's degree OR certification in a related allied health profession from an appropriately accredited institution (i.e. RN, MT, PA, RT) is preferred, but individuals with commensurate experience will be considered.
  • Experience with Electronic Data Capture (EDC) system(s) is required.
  • Experience with Oracle Inc.'s Inform™ EDC system is preferred.
  • Oncology and/or inflammatory therapeutic area experience is preferred.
  • Project management experience (within Data Management) is preferred.
  • Work history at a Clinical Research Organization (CRO) or CRO management experience in data management is preferred.

#LI-AP1
#LI-REMOTE
We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.
All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not.
Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office.
***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***

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