Celerion Jobs Hiring Now
Celerion is hiring for 31 open roles on Migrate Mate as of July 16, 2026, concentrated in laboratory research and clinical trials & medical research. Migrate Mate updates Celerion's live openings daily. Celerion is a clinical research organization specializing in early-phase drug development, bioanalytical science, and pharmacokinetic studies for pharmaceutical and biotech clients.
Find Celerion JobsOverview
Celerion hiring data on Migrate Mate, as of July 16, 2026.
- Open jobs
- 31
- Top team
- Laboratory Research
- Seniority
- Mid to senior level
- Work type
- 26% remote or hybrid
- Top location
- Lincoln
Open Roles at Celerion
Showing 25 of 31+ Celerion jobs
- Review protocol and Investigator Brochure for subject safety, scientific, and operational feasibility of study. Provide input to sponsor as indicated.
- Complete FDA 1572 and financial disclosure forms.
- Attend study initiation meetings with sponsor.
- Communicate with Institutional Review Board during protocol approval process and subject safety issues.
- Explain study to subject and answer questions, ensure proper consent, and perform screening examination.
- Final review of all screening data and authorization of subjects to be enrolled in the study.
- 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. Review pre-dose lab work, ECGs, and other study data and determine appropriate action plan based on these results. Review safety data with sponsor.
- Compose SAE and other reporting documents as indicated.
- Review and sign Case Report Forms and final Clinical Study Reports.
- Review all serious adverse events and SUSARs to the Sponsor and IRB within statutory timelines
- Data review of all end-of-study data to determine if re-checks are necessary
- Safety-monitoring – perform end-of-study physical exams and follow-up ongoing adverse events
- Case Report Forms review – review and sign all case report forms at end of study
- Assist in on-site client review of case report forms
- Assist with identifying and maintaining a network of physician specialists to contract on studies.
- Present Celerion’s capabilities and experience during sponsor meetings and events.
- Assist in the design of study and time/event schedules involving special medical procedures
- Function as a medical/clinical informational resource for the site.
- Assist other departments with development of SOPs, training plans, etc.
- Facilitate emergency response training and review of clinical safety procedures.
Qualifications
- MD or DO degree and current state license.
- 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
- Clinical research experience preferred
- Able to work a flexible schedule
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.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
- Review protocol and Investigator Brochure for subject safety, scientific, and operational feasibility of study. Provide input to sponsor as indicated.
- Complete FDA 1572 and financial disclosure forms.
- Attend study initiation meetings with sponsor.
- Communicate with Institutional Review Board during protocol approval process and subject safety issues.
- Explain study to subject and answer questions, ensure proper consent, and perform screening examination.
- Final review of all screening data and authorization of subjects to be enrolled in the study.
- 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. Review pre-dose lab work, ECGs, and other study data and determine appropriate action plan based on these results. Review safety data with sponsor.
- Compose SAE and other reporting documents as indicated.
- Review and sign Case Report Forms and final Clinical Study Reports.
- Review all serious adverse events and SUSARs to the Sponsor and IRB within statutory timelines
- Data review of all end-of-study data to determine if re-checks are necessary
- Safety-monitoring – perform end-of-study physical exams and follow-up ongoing adverse events
- Case Report Forms review – review and sign all case report forms at end of study
- Assist in on-site client review of case report forms
- Assist with identifying and maintaining a network of physician specialists to contract on studies.
- Present Celerion’s capabilities and experience during sponsor meetings and events.
- Assist in the design of study and time/event schedules involving special medical procedures
- Function as a medical/clinical informational resource for the site.
- Assist other departments with development of SOPs, training plans, etc.
- Facilitate emergency response training and review of clinical safety procedures.
Qualifications
- MD or DO degree and current state license.
- 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
- Clinical research experience preferred
- Able to work a flexible schedule
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.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
Job Roles at Celerion
Working at Celerion
Celerion's 31 open roles are mid to senior level, and about 26% are remote or hybrid. The most active teams are laboratory research, clinical trials & medical research, and biotech & life sciences. Celerion is a contract research organization focused on early-phase clinical trials, bioanalytical testing, and drug metabolism studies that support pharmaceutical development programs. Roles span clinical research, data science, quality assurance, pharmacokinetics, and laboratory science. Most Celerion roles are based in Lincoln, with some in Tempe and Phoenix.
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Browse jobs by roleCelerion Jobs: Frequently Asked Questions
How many jobs is Celerion hiring for right now?
Celerion is hiring for 31 open roles on Migrate Mate as of July 16, 2026, updated daily, concentrated in laboratory research and clinical trials & medical research. Positions range from clinical research coordinators and principal investigators to data management, quality assurance, and laboratory science roles across multiple sites.
What kinds of roles does Celerion hire for?
The most active teams are laboratory research, clinical trials & medical research, and biotech & life sciences. Celerion hires across clinical research, bioanalytical science, pharmacokinetics, data management, quality assurance, and technology functions. Roles include clinical research nurses, coordinators, associate scientists, instrument scientists, EDC programmers, and clinical data managers. Most postings are mid to senior level, though entry-level and senior leadership positions also appear regularly.
Are Celerion jobs remote or in-person?
A mix of remote and on-site. About 26% of Celerion's open roles on Migrate Mate are remote or hybrid as of July 16, 2026, with the rest based in Lincoln. Each Celerion listing shows its work location so you can filter before applying.
How do I apply to a job at Celerion?
Find a Celerion role on Migrate Mate, then follow the listing directly through to Celerion's own careers page to complete your application. Celerion manages its own hiring process, including screening, interviews, and offers. Migrate Mate keeps the listings current so the role you click is open at that moment.
Does Celerion hire entry-level?
Most of Celerion's open roles on Migrate Mate are mid to senior level as of July 16, 2026. Entry-level openings are limited. Check individual Celerion listings for stated experience requirements.
Where is Celerion hiring?
Most Celerion roles are based in Lincoln, with some in Tempe and Phoenix, and about 26% offer remote or hybrid work as of July 16, 2026. Migrate Mate shows the location on each listing.