Celerion

Celerion

Principal Investigator

Lincoln, NE · Principal

Sponsorship not specifiedDetected 597 days ago
SwiftGCPClinical TrialsClinical ResearchFDA RegulatoryResearch

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odds of building a lasting career here

37Risky
Cap-exempt (no lottery)0
Sponsors this role80
Entry-level history0
PERM / green-card track0
Lottery odds40
Fits your clock70

Thin sponsorship signal and lottery-bound. A low-probability bet with your clock running. Prioritize cap-exempt roles and proven entry-level sponsors first.

Lottery odds assume a STEM candidate.

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Employer immigration record

from this employer's Department of Labor filings

Files H-1B transfers

2 transfer filings in the last year, covering 2 workers. Median labor-condition decision: 22 days. An employer that already files transfers is one that can take over an existing H-1B.

Sourced from Department of Labor LCA, PERM and prevailing-wage disclosure data. Employer matching is by name, so figures may be split across an employer's legal entities. Absence of a filing means none appears in our copy of the data, not that none exists.

Community outcomes

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About the role

  • Celerion is committed to swift, exceptional clinical research through translational medicine.
  • Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
  • The PI is responsible for the safety of subjects who participate in clinical trials and for executing the study according to the IRB-approved protocol and applicable FDA and GCP regulations.

Responsibilities

  • Perform scheduled per protocol, and unscheduled per adverse event, physicals during study conduct. · Manage adverse events/clinical evaluation of subjects and determine adverse event relationship to investigational product, severity, and etiology.

Requirements

  • MD or DO degree and current state license.
  • If you are a Gmail user and you chose to receive e-mails from @celerion.com, please check your Spam folder regarding the status of your application, including requests for availability and interview invitations.
  • Basic Life Support and Advanced Cardiac Life Support certification
  • Successful completion of an ACGME residency program in family medicine, internal medicine, or emergency medicine.
  • Hold a DEA certificate for schedule II medications
  • 3-5 years of medical/clinical experience preferred
  • Able to work a flexible schedule
  • If you are a Gmail user and you chose to receive e-mails from @celerion.com, please check your Spam folder regarding the status of your application, including requests for availability and interview invitations. Additionally, ensure you mark Celerion e-mails as "Not Junk". Celerion Values: Integrity Trust Teamwork Respect Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability. Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as "Not Junk" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.

Nice to have

  • Clinical research experience preferred

Equal opportunity

  • Celerion Values: Integrity Trust Teamwork Respect Celerion is an Equal Opportunity Employer.

Visa & Work Authorization

  • Provide input to sponsor as indicated

This listing is sourced directly from Celerion's careers page and normalized into a canonical job model.