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Summary
About the Role
About You
- Bachelor's degree and/or professional license in a medical or scientific field (RN, BS, MS, MPH) or equivalent experience.
- 1-3 years experience in a hospital/clinical setting or interpreting medical or clinical results.
- Professional writing and editing skills for accurate and concise reporting of clinical trial results.
- Detail-oriented, thorough, and methodical.
- Ability to work without close supervision and under pressure.
- Excellent communication/interpersonal skills.
- Knowledge of medical, pharmaceutical, and/or clinical research concepts.
- Ability to multi-task and respond rapidly to changing priorities and aggressive timelines.
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