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Manager Bioinformatics Jobs in Illinois (NOW HIRING)

Tempus

Manager, Regulatory Submissions (Remote)

Chicago, IL · On-site +1

$110K - $150K/yr

Our Manager of Regulatory Affairs will work closely with our scientists, engineers, clinicians ... Ability to work well with quality, clinical, medical, bioinformatics, and laboratory teams across a ...

Saransh Inc

Lead Quality Engineer

Mettawa, IL · On-site

Tosca Administration & Support · Run and validate test cases and modules. · Manage sync settings ... Domain Application · Apply knowledge of Bioinformatics, R&D, Preclinical, and Clinical domains to ...

Tempus

Senior Software Engineer II, Data Products

Chicago, IL · On-site

$126K - $166K/yr

... bioinformatics scientists, ML and Agent developers to rapidly develop, deploy, and operate their ... Use exemplary stakeholder management skills to work closely with Product Managers to translate ...

Tempus AI, Inc.

Senior Scientist R&D

Chicago, IL · On-site

$94 - $135/hr

... bioinformatics, quality control, regulatory affairs, and the clinical lab. What you'll do ... Manage and lead generation of R&D design documents * Lead validation team from project inception ...

New

University of Utah

Research Science Management

Campus, IL · On-site

$91K - $209K/yr

Build strong partnerships with related shared resources (e.g., bioinformatics, research informatics ... Proven leadership experience managing teams and complex operations. * Strong communication and ...

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All JobsBioinformatics JobsManager Bioinformatics JobsManager Bioinformatics Jobs in Illinois

Manager Bioinformatics information

What is the difference between Manager Bioinformatics vs Bioinformatics Scientist?

AspectManager BioinformaticsBioinformatics Scientist
Required CredentialsBachelor's or Master's in Bioinformatics, Biology, or related field; leadership experienceMaster's or PhD in Bioinformatics, Computational Biology, or related field
Work EnvironmentTeam leadership, project management, cross-department collaborationData analysis, algorithm development, research-focused
Employer & Industry UsageBiotech, pharma, research institutions, biotech startupsResearch labs, academia, biotech companies
Common Search & ComparisonYesYes

The main difference between a Manager Bioinformatics and a Bioinformatics Scientist lies in their roles. Managers oversee teams, coordinate projects, and handle leadership responsibilities, while Bioinformatics Scientists focus on data analysis, developing algorithms, and conducting research. Both roles require strong technical skills, but the Manager Bioinformatics position emphasizes leadership and project management within the bioinformatics field.

What are the most commonly searched types of Bioinformatics jobs in Illinois?

The most popular types of Bioinformatics jobs in Illinois are:

What cities in Illinois are hiring for Manager Bioinformatics jobs?

Cities in Illinois with the most Manager Bioinformatics job openings:

Manager Bioinformatics jobs near you

Manager, Regulatory Submissions (Remote)

Tempus

Chicago, IL • On-site, Remote

$110K - $150K/yr

Full-time

Re-posted 6 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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