Full-Time
Associate Scientific /Technical Writer
Posted on 11/28/2024
Celerion
1,001-5,000 employees
Clinical research organization for drug development
Entry, Junior
No H1B Sponsorship
Lincoln, NE, USA
Office-based position; candidates must be local to Lincoln, NE.
- Bachelor’s degree or an Associate degree in a science-related field
- Medical, clinical or bioanalytical laboratory experience is highly preferred
- Must be proficient with Microsoft Word and Excel
- Excellent writing skills
- Strong attention to detail
- Ability to adapt to change
- Experience working with Watson LIMS system or other databases
- Knowledge of bioanalytical testing a plus
- Ensure all scientific documents are prepared, maintained and controlled at the highest standard of quality and compliance before they are submitted to both external and internal clients
- Work with multiple electronic databases to extract data and generate quality scientific documents to follow existing style guides and templates
- Work with various departments moving the physical files from one location to another as the document works through the life cycle
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
N/A
6 month growth
↑ 11%1 year growth
↑ 11%2 year growth
↑ 13%
Simplify's Take
What believers are saying
- Celerion's expansion into GLP/GCP compliant molecular and cell biology testing positions it well to support the growing field of cell and gene therapies.
- The appointment of Jo Goodman as VP of Bioanalytical Services brings extensive industry experience, potentially driving innovation and enhancing service delivery.
- H.I.G. Capital's acquisition of Celerion could provide additional resources and strategic direction, fostering further growth and development.
What critics are saying
- The acquisition by H.I.G. Capital may lead to changes in company culture or strategic priorities, potentially causing uncertainty among employees.
- The competitive landscape of CROs requires Celerion to continuously innovate and maintain high standards to retain its leadership position.
What makes Celerion unique
- Celerion's expertise in early phase drug development and advanced bioanalytical sciences, particularly in metabolite profiling using HR MS, sets it apart from other CROs.
- The company's consistent recognition with CRO Leadership Awards highlights its reputation for quality, capabilities, and reliability in the industry.
- Celerion's recent CLIA certification enhances its bioanalytical laboratory capabilities, allowing it to conduct high-complexity testing and diagnostic services.
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