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
Lincoln, NE, USA
Position requires onsite presence in Lincoln, NE.
- You will have a Bachelor’s degree in a related discipline or BSN required. Celerion experience may be considered in lieu of degree in some situations.
- Industry experience and knowledge of medical terminology preferred.
- Demonstrated organizational, time management and multi-tasking skills required
- Shown ability to handle multiple priorities
- Excellent oral and written communication skills
- You will work without close supervision
- Ability to work flexible hours required for study conduct
- You will utilize customer service skills
- Clinical Research experience useful, but not required
- You are responsible for the overall management of Clinical Studies to include: on-time performance with defect-free execution, independently conducting bioequivalency and bioavailability studies, working with support divisions to ensure timelines are being met in clinical studies (i.e. recruiting, data management, statistics), 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, and organizing study logistics and personnel.
- In addition, you will be present at critical events and dosings of study.
- You will build client relationships that result in additional business, you will craft and edit reports, respond to client issues, concerns and requests, adhere to milestone guidelines, and ensure profitability by maintaining profitability of team through a budgeting and expense control on a total and individual study basis.
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
↑ 11%1 year growth
↑ 11%2 year growth
↑ 15%
Simplify's Take
What believers are saying
- Celerion's global capabilities support the growing trend of decentralized clinical trials.
- The rise of precision medicine aligns with Celerion's expertise in specialized bioanalytical services.
- Expansion into GLP/GCP compliant testing positions Celerion well in cell and gene therapy markets.
What critics are saying
- Emerging CROs in Asia offer cost-effective solutions, threatening Celerion's market share.
- H.I.G. Capital's acquisition may disrupt client relationships or alter service offerings.
- Regulatory hurdles could delay the rollout of new GLP/GCP compliant testing services.
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 offers comprehensive services including trial design, bioanalytical sciences, and regulatory affairs.
Help us improve and share your feedback! Did you find this helpful?