Full-Time
Clinical Research Coordinator
Confirmed live in the last 24 hours
Celerion
1,001-5,000 employees
Clinical research organization for drug development
Entry, Junior
Lincoln, NE, USA
Position requires onsite presence in Lincoln, NE.
- Bachelor’s degree in a related discipline or BSN required
- Demonstrated organizational, time management and multi-tasking skills required
- Shown ability to handle multiple priorities
- Excellent oral and written communication skills
- Ability to work flexible hours required for study conduct
- You will utilize customer service skills
- Overall management of Clinical Studies
- Independently conducting bioequivalency and bioavailability studies
- Working with support divisions to ensure timelines are being met in clinical studies
- Organizing study initiation meetings to plan execution of study
- Facilitating study review meetings for pre-study, in-process and post study review
- Problem solving as needed during study conduct
- Meeting with clients as needed throughout study
- Organizing study logistics and personnel
- Present at critical events and dosings of study
- Crafting and editing reports
- Responding to client issues, concerns and requests
- Adhering to milestone guidelines
- Ensuring profitability by maintaining profitability of team through budgeting and expense control
- Industry experience and knowledge of medical terminology preferred
- Clinical Research experience useful, but not required
Celerion specializes in early phase drug development as a clinical research organization (CRO). The company provides a range of services to pharmaceutical and biotechnology companies, including clinical trial design, feasibility studies, project management, and regulatory affairs. Celerion utilizes advanced bioanalytical sciences, particularly in metabolite profiling and identification through High Resolution Mass Spectrometry (HR MS), to support critical drug development decisions. What sets Celerion apart from its competitors is its extensive experience of over 40 years and its focus on delivering swift and high-quality research. The goal of Celerion is to help clients accelerate the process of bringing new treatments to market, ultimately benefiting patients around the world.
Company Stage
Acquired
Total Funding
N/A
Headquarters
Lincoln, Nebraska
Founded
2010
6 month growth
↑ 4%1 year growth
↑ 4%2 year growth
↑ 4%
Simplify's Take
What believers are saying
- Rising demand for early-phase trials due to personalized medicine boosts Celerion's market.
- Advancements in AI enhance Celerion's bioanalytical data analysis and metabolite profiling.
- Expansion into cell and gene therapy markets aligns with Celerion's service offerings.
What critics are saying
- Emerging CROs offering similar services at lower costs threaten Celerion's market share.
- Regulatory changes in the EU and China could increase compliance costs for Celerion.
- Talent shortages in the pharmaceutical sector may hinder Celerion's ability to retain staff.
What makes Celerion unique
- Celerion specializes in early-phase drug development with over 40 years of experience.
- The company excels in metabolite profiling using High Resolution Mass Spectrometry (HR MS).
- Celerion's global operations offer comprehensive services from trial design to regulatory affairs.
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Benefits
Flexible Work Hours