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Summary
About the Role
About You
- Ability to quickly identify key proposal and budgeting parameters based on knowledge and experience.
- Ability to prioritize workflow quickly and efficiently against deadlines.
- Strong verbal and written communication skills.
- Adept at cross-functional team collaboration, including the ability to interact with all levels of the organization.
- BA/BS in business/finance/life sciences or equivalent education and experience.
- 3-5 years of experience in early phase clinical research.
- 3-5 years of experience reading, reviewing, and understanding information contained within clinical research protocols.
- Previous experience with clinical trial proposal processes and budget generation.
Celerion, a leader in early clinical research, delivers Applied Translational Medicine. Celerion applies our expertise and experience to translating information gained in research discoveries, to knowledge of drug action and effect in humans to support early drug development decisions and the clinical pharmacology labeling of new medicines. With over 50 years of experience and 600 global clinic beds (including 24 in-hospital), Celerion conducts and analyzes First-in-Human, clinical proof-of-concept, cardiovascular safety (TQT, robust QT), ADME and NDA-enabling clinical pharmacology studies. Celerion provides expertise on modeling and simulation, study design, medical writing (protocols and reports), clinical data sciences, biostatistics, and PK/PD analysis as well as small and large molecule bioanalytical assays through clinical drug development. Regulatory, drug development and program management complement Celerion’s service offerings. Our operations are strategically located in: Lincoln, Nebraska (Corporate Headquarters) Philadelphia, Pennsylvania Phoenix, Arizona Belfast, Northern Ireland,UK Zurich, Switzerland Vienna, Austria Richmond, Virginia Montreal, Quebec, Canada For more information, visit: www.celerion.com