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Work From Home Clinical Programmer Medidata Rave Jobs in Elgin, IL

Next Step Systems

FPGA Engineer - Work From Home

Chicago, IL · On-site +1

$133K - $172K/yr

FPGA Engineer - Work From Home We are seeking a talented and self-motivated FPGA Engineer to join a growing hardware engineering team. Our culture emphasizes teamwork and focuses on continuous ...

Globe Life Inc.

Work From Home Sales

Chicago, IL · Remote

About Us For over 70 years, we've proudly supported union members and working families as a 100% union-based organization. Our mission is clear: protect, serve, and deliver real solutions families ...

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All JobsClinical Programmer Medidata Rave JobsWork From Home Clinical Programmer Medidata Rave JobsWork From Home Clinical Programmer Medidata Rave Jobs in Elgin, IL

Work From Home Clinical Programmer Medidata Rave information

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How much do work from home clinical programmer medidata rave jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for work from home clinical programmer medidata rave in Elgin, IL is $64.03, according to ZipRecruiter salary data. Most workers in this role earn between $52.98 and $72.45 per hour, depending on experience, location, and employer.

What is a work from home clinical programmer Medidata Rave?

A Work From Home Clinical Programmer Medidata Rave is a professional who remotely designs, builds, and manages electronic data capture systems for clinical trials using Medidata Rave software. They are responsible for creating study databases, programming edit checks, and ensuring data integrity and regulatory compliance. These programmers work closely with clinical teams to support the collection, analysis, and reporting of clinical trial data, all while working from a remote location. Their expertise in Medidata Rave and clinical data management is essential for the successful execution of clinical studies.

What does a work from home clinical programmer Medidata Rave do?

As a remote Clinical Programmer specializing in Medidata Rave, you will frequently interact with data managers, clinical research associates, and biostatisticians through virtual meetings and collaboration tools. You'll be responsible for programming study databases, building and validating electronic case report forms (eCRFs), and troubleshooting data discrepancies. Effective communication and proactive problem-solving are key, as you may need to quickly address queries or implement changes based on feedback. Most organizations use platforms like Microsoft Teams, Slack, or email to facilitate real-time collaboration, ensuring that despite working remotely, you remain integrated with the wider study team.

What are the key skills and qualifications needed to thrive as a work from home clinical programmer Medidata Rave?

To thrive as a Work From Home Clinical Programmer specializing in Medidata Rave, you need a solid background in clinical data management, programming (such as SQL, SAS, or R), and a degree in life sciences or a related field. Familiarity with Medidata Rave EDC, CDISC standards (SDTM, CDASH), and certifications like Medidata Rave Certified Study Builder are often required. Strong attention to detail, problem-solving abilities, and effective remote communication are vital soft skills for excelling in this role. These competencies ensure accurate data capture, regulatory compliance, and seamless collaboration across globally distributed clinical research teams.

What is the difference between Work From Home Clinical Programmer Medidata Rave vs Work From Home Clinical Data Coordinator?

AspectWork From Home Clinical Programmer Medidata RaveWork From Home Clinical Data Coordinator
Required CredentialsBachelor's in Life Sciences, Clinical Data Management, or related field; experience with Medidata RaveBachelor's in Life Sciences, Clinical Data Management; some roles may require certification
Work EnvironmentRemote, primarily using Medidata Rave for data entry and managementRemote or hybrid, managing data entry, cleaning, and query resolution
Employer & Industry UsagePharmaceuticals, CROs, biotech firms using Medidata RavePharmaceuticals, CROs, clinical research organizations

While both roles involve clinical data management, the Clinical Programmer focuses on configuring and programming data capture in Medidata Rave, whereas the Data Coordinator handles data entry, cleaning, and query resolution. Both roles are often remote and require similar educational backgrounds, but their specific responsibilities and tools differ.

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Work From Home Clinical Programmer Medidata Rave jobs near you
Infographic showing various Work From Home Clinical Programmer Medidata Rave job openings in Elgin, IL as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 20% Part Time, and 3% Contract. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $133,183 per year, or $64 per hour.

Clinical Data Management Specialist

Hollister Incorporated

Libertyville, IL • Remote

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 8 days ago

Abercrombie & Fitch rating

6.2

Company rating: 6.2 out of 10

Based on 155 frontline employees who took The Breakroom Quiz

51st of 104 rated fashion retailers

Job description

We Make Life More Rewarding and Dignified 

Location: Libertyville
Department: Clinical Affairs 

Summary

The Specialist, Clinical Data Management (CDM) is a leader in supporting clinical studies for Hollister Incorporated medical device products and services. The CDM leads all aspects of clinical data management from study planning to database lock including EDC design, data review/cleaning, query management, data reconciliation, and data transfer. The CDM regularly collaborates with Global Clinical Affairs (GCA) study team members (Clinical Project Management, Biostatistics, Clinical Operations, Clinical Scientist) and cross-functional departments to ensure high data quality. The position operates under minimal supervision and independently evaluates, selects, and applies data management practices to a variety of research projects.

Responsibilities

Design and Planning

  • Lead the development of data management sections of clinical protocol and corresponding Case Report Forms (CRFs).
  • Develop and maintain data management essential documentation for the Trial Master File including, but not limited to; Data Management Plan, study-specific monitoring guidelines, edit checks, and user access forms, ensuring compliance with regulatory requirements
  • Support each clinical study and project team by ensuring data management plans, questionnaire development, and data handling activities are aligned to support the study objectives.
  • Participate in study team meetings

EDC Administration

  • Design and program clinical study databases in EDC System including but not limited to CRFs, edit checks, data dictionaries, queries/alerts, and managing user roles based on the clinical protocol
  • Lead User Acceptance Testing (UAT) to validate build specifications
  • Train clinical research personnel on the study-specific CRF, EDC/ePRO, and other project related items as needed.
  • Lead database clean, lock, export, and archiving activities.
  • Oversee data management vendor relationships including EDC partners and CROs supporting DM tasks
  • Continuously assess and enhance the EDC systems to improve efficiency and data quality

Data Monitoring

  • Monitor clinical data to resolve queries and data discrepancies throughout each study according to Clinical Protocol and/or Data Management Plan
  • Coordinates AE/DD reconciliation with PI
  • Identify and communicate data issues and/or query trends to study team and/or management.
  • Assist with developing metrics on study progress and routinely report out to study team and management.

Compliance and Process

  • Ensure data management activities comply with Good Clinical Practice (GCP), regulatory requirements, and internal standard operating procedures.
  • Contribute to the maintenance of GCA's data management procedures and work instructions
  • Responsible for leading or collaborating on process improvement initiatives within department
  • Meet study timelines with a high degree of quality
  • Other duties as needed or required. 
Essential Functions of the Role
  • Communicate effectively via email, phone, and virtual platforms.
  • Prepare reports and dashboards for internal stakeholders.
  • Ensure data accuracy and confidentiality in compliance with company and legal standards.
  • Manage multiple priorities and deadlines in a fast-paced environment.
  • Demonstrate initiative in identifying process improvements or automation opportunities.
  • Serve as a point of contact for internal and external stakeholders.
  • Resolve inquiries and issues with professionalism and discretion.
  • Adhere to company policies, including those related to ADA, data privacy, and ethics.
  • Maintain secure handling of sensitive information.
Education & Work Requirements
  • Bachelor's Degree with 2-5 years of related experience
Education & Work Preferences
  • Minimum of 2 years EDC database programming and Data Monitoring experience
  • Minimum of 2 years medical device and/or pharmaceutical clinical research experience
  • Certified Clinical Data Manager (CCDM) via SCDM or similar preferred
  • Equivalent combination of education, training and work experience may be accepted in lieu of degree.
  • Experience with EDC Systems (e.g. Medrio, Clinpal, Medidata Rave, etc.) required
  • Understanding of clinical research regulations required
  • Experience in questionnaire development, database structure, and data management processes
  • Experience with Microsoft Suite Applications (Word, PowerPoint, Excel, Teams)
  • Knowledge relating to continence care, critical care and/or ostomy a plus
Competencies
  • Be Agile - Innovates and adapts quickly, approaching change with curiosity while persisting through obstacles.
  • Be Customer Centric - Considers the needs, experiences and feedback of customers in all we do.
  • Be People-Focused - Builds trust and collaborates with an inclusive and empathetic approach.
  • Be Performance Driven - Operates with an ownership mindset, driving meaningful outcomes.
  • Live The Schneiders' Legacy, Our Noble Purpose - Passionately serves Our Mission and Vision, while demonstrating the Immutable Principles.

Benefits Statement

Our Total Rewards package in aggregate is above market and includes competitive pay, paid time off programs, peer-to-peer recognition, health and life insurance, wellness programs and incentives, and generous retirement savings.

  • The anticipated base pay range for this position is $77,000 - $120,000 yearly. The actual salary varies based on applicant's location, education, experience, skills, abilities, and other legitimate business factors.
  • If applicable: This position is also eligible to participate in the Hollister Secure Start Bonus Plan.
  • The Company's health and welfare benefits include medical, prescription, dental, vision, spending/savings accounts, disability, company paid (parental and caregiver) leaves, statutory leaves/disability programs, accident, life, wellbeing, education assistance, adoption assistance, and voluntary benefit programs. 
  • The Company's 401(k) Retirement Savings Plan includes: auto-enrollment, ROTH, vesting and eligible participants "safe harbor" matching contributions. 
  • The Company's paid time off benefits include: 11 paid holidays, paid vacation based on length of service and exempt/non-exempt status, and sick days based on statutory requirements and/or exempt/non-exempt status. 
  • The Company's additional benefits include: education assistance and adoption assistance benefit programs. 

About Hollister Incorporated
Hollister Incorporated is an independent, employee-owned company that develops, manufactures and markets healthcare products worldwide. The company spearheads the advancement of innovative products for ostomy care, continence care and critical care, and also creates educational support materials for patients and healthcare professionals. Headquartered in Libertyville, Illinois, Hollister has manufacturing and distribution centers on three continents and sells in nearly 80 countries. Hollister is a wholly owned subsidiary of The Firm of John Dickinson Schneider, Inc., and is guided both by its Mission to make life more rewarding and dignified for people who use our products and services, as well as its Vision to grow and prosper as an independent, employee-owned company, and in the process, to become better human beings.

EOE Statement
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

Job Req ID: 36304

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