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Remote Registration Jobs in Wheaton, IL (NOW HIRING)

Tempus

Manager, Regulatory Submissions (Remote)

Chicago, IL · On-site +1

$110K - $150K/yr

Ex-US, CE Marking, UKCA registration, performance studies as required under IVDR and MDR * Software ... remote $110,000-$150,000 The expected salary range above is applicable if the role is performed ...

PainPoint

Customer Service Representative

Chicago, IL · On-site +1

$18/hr

Remote Looking for a rewarding career where you can make an impact every day? Join DxTx Pain ... Register and schedule new patients; send appropriate materials prior to appointments * Reschedule ...

Evangelical Covenant Church

Events Registrar

Chicago, IL · On-site +1

... registration for all Covenant Events, post-event evaluation process, and on-site events support ... Environment Conditions Able to work well in professional office settings and remote work settings.

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Showing results 21-40

All JobsRegistration JobsRemote Registration JobsRemote Registration Jobs in Wheaton, IL

Remote Registration information

See Wheaton, IL salary details

$7

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$46

How much do remote registration jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for remote registration in Wheaton, IL is $21.59, according to ZipRecruiter salary data. Most workers in this role earn between $16.01 and $22.55 per hour, depending on experience, location, and employer.

What is a remote registration?

A Remote Registration job typically involves assisting individuals or organizations with registering for services, programs, or events from a remote location, often online or by phone. Responsibilities may include collecting and verifying personal information, entering data into registration systems, answering questions, and ensuring a smooth registration process. These roles are common in healthcare, education, and event management sectors, allowing employees to work from home or another remote location. Strong communication, computer, and organizational skills are essential for success in this role.

What are the key skills and qualifications needed to thrive as a remote registration specialist?

To thrive as a Remote Registration Specialist, you need strong attention to detail, data entry accuracy, and familiarity with patient registration processes, often supported by a high school diploma or equivalent. Experience with electronic health record (EHR) systems, scheduling software, and secure communication platforms is typically required. Excellent communication, customer service, and problem-solving skills help build rapport with patients and resolve issues remotely. These competencies ensure efficient, accurate patient intake and a positive experience, which are critical for healthcare operations.

What are some common challenges faced in a remote registration role, and how can they be addressed?

In a Remote Registration role, one common challenge is ensuring clear communication with clients or patients who may have varying levels of technical proficiency. Additionally, verifying documentation and maintaining data accuracy without face-to-face interaction can be difficult. These challenges can be addressed by using secure, user-friendly platforms, providing clear instructions, and double-checking information for accuracy. Regular virtual check-ins with the team can also help maintain consistency and support.

What is the difference between Remote Registration vs On-site Registration?

AspectRemote RegistrationOn-site Registration
Work EnvironmentOnline, virtual processIn-person at event or location
Required CredentialsBasic identification, digital formsValid ID, physical documents
Usage in IndustryCommon for conferences, webinars, virtual eventsTypical for physical events, trade shows
Employer/Organizer PreferenceAllows remote access, flexible timingRequires physical presence, on-site verification

Remote Registration involves completing the registration process online from anywhere, offering convenience and flexibility. On-site Registration requires physical presence at the event location, often involving in-person verification. Both methods are used across industries, but remote registration is increasingly popular for virtual events, while on-site registration remains standard for physical gatherings.

What are the most commonly searched types of Registration jobs in Wheaton, IL?

The most popular types of Registration jobs in Wheaton, IL are:

What are popular job titles related to Remote Registration jobs in Wheaton, IL?

For Remote Registration jobs in Wheaton, IL, the most frequently searched job titles are:

What job categories do people searching Remote Registration jobs in Wheaton, IL look for?

The top searched job categories for Remote Registration jobs in Wheaton, IL are:

What cities near Wheaton, IL are hiring for Remote Registration jobs?

Cities near Wheaton, IL with the most Remote Registration job openings:

Remote Registration jobs near you
Infographic showing various Remote Registration job openings in Wheaton, IL as of August 2026, with employment types broken down into 1% As Needed, 49% Full Time, 48% Part Time, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $44,910 per year, or $21.6 per hour.

Manager, Regulatory Submissions (Remote)

Tempus

Chicago, IL • On-site, Remote

$110K - $150K/yr

Full-time

Re-posted 23 days ago

Job description

Passionate about precision medicine and advancing the healthcare industry?
Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.
At Tempus, we are building a regulatory team that will adopt creative approaches as we develop regulated medical devices and seek marketing authorization from FDA. Our Manager of Regulatory Affairs will work closely with our scientists, engineers, clinicians, quality professionals, and legal team to support our efforts to advance personalized medicine.
Responsibilities
  • Developing and leading global regulatory strategies to support business objectives
  • Leading and assisting with submissions and correspondence with global regulatory authorities, including 510(k), PMA, De Novo authorizations, IDE, MDR CE marking, UKCA marking, etc.
  • Establishing processes for efficiently addressing the requirements of multiple regulatory frameworks at scale
  • Developing and executing premarket and postmarket regulatory project plans and strategies, including assessments of change controls
  • Working closely with cross-departmental subject matter experts to guide the creation of documentation needed for regulatory applications and internal records
  • Work closely with business leadership to ensure regulatory strategy aligns with commercial goals
  • Making regular reports to our executive team, operationalizing leadership direction quickly and efficiently

What your background might look like:
  • Oncology IVD, IUO, and CDx experience required
  • Experience with complex medical devices, such as some combination of:
    • Genomics
    • NGS
    • Software and artificial intelligence based devices
    • Clinical decision support software
    • Oncology
  • Experience with:
    • Premarket Approval (PMA) applications, de novo Requests for Reclassification, 510(k)s, Investigational Device Exemption (IDE) requirements
    • Ex-US, CE Marking, UKCA registration, performance studies as required under IVDR and MDR
    • Software validation and risk management
    • Cybersecurity in medical devices
    • Machine learning validation requirements
    • Lifecycle management of medical devices/IVDs
    • Changes to medical devices or IVDs, including those that trigger reporting or regulatory submissions
    • Relevant sections of 21 CFR 820/ISO 13485, 21 CFR 812, CAP/CLIA
    • Strong communication, presentation. and interpersonal skills
    • Guiding cross-functional teams of subject matter experts
    • Working in a startup-like environment
    • Interacting with regulators
    • Ability to work well with quality, clinical, medical, bioinformatics, and laboratory teams across a variety of therapeutic areas
    • Responsive to feedback, willing to change direction, and able to identify creative solutions to meet business and regulatory needs
    • Excellent attention to detail
    • Strong project management skills and the ability to execute on project plans in a fast-paced environment
  • Scientific background
    • PhD preferred.
    • Minimum of 5+ years of experience in Regulatory Affairs experience related to medical devices
    • Knowledge of engineering concepts and biology with ability to evaluate device performance data and develop testing plans

#LI-remote
$110,000-$150,000
The expected salary range above is applicable if the role is performed from Illinois and may vary for other locations (California, Colorado, New York). Actual salary may vary based on qualifications and experience. Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and other benefits depending on the position.
We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

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