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
You match the following Celerion's candidate preferences
Employers are more likely to interview you if you match these preferences:
- 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 uses advanced bioanalytical techniques, particularly High Resolution Mass Spectrometry (HR MS), for metabolite profiling and identification, which enhances their research capabilities. This focus on bioanalytical sciences and their extensive experience allows Celerion to assist clients in making informed decisions during the early stages of drug development. Unlike many competitors, Celerion emphasizes speed and quality in their research processes, aiming to help clients bring new treatments to market more quickly, 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
- Growing demand for early-phase trials due to personalized medicine boosts Celerion's market.
- Advancements in bioanalytical technologies align with Celerion's expertise, enhancing service precision.
- Expansion in cell and gene therapy markets increases demand for Celerion's specialized services.
What critics are saying
- Emerging CROs in Asia offer cost-effective solutions, threatening Celerion's market share.
- AI advancements in drug discovery may reduce demand for traditional CRO services.
- Pharmaceutical industry consolidation could lead to fewer clients and larger contracts.
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