Responsibilities
- Data analysis and interpretation
- Provide input on data collection methods and coordinate customized electronic database transmissions to
Sponsors - Support the randomization process by generating randomization schedules and randomizations plans
- Develop statistical analysis plans for simple to complex studies including table shells and, when appropriate, other programming plans
- Direct and oversee the execution of planned statistical analysis and summarization for simple to complex studies (including tables, figures, and data listings) independently
- Write statistical methods and results sections of reports for assigned projects
- Review draft report for consistency and completeness
- Effectively communicate with colleagues and clients regarding timelines, deliverables, and commitments
- Provide programming assistance, as applicable
- Interact with internal departments (e.g., data management, project management, etc.)
- Lead and/or participate in functions required to ensure success of department and/or market segment team
Requirements
- Master's degree in Statistics-related field and 3+ years industry experience or the equivalent OR
Bachelor's degree in Statistics-related field and 3+ years industry related experience and 4+years SAS
programming experience of the equivalent - Proficiency with SAS programming
- Ability to organize multiple priorities
- Excellent communication and leadership skills
- Demonstrated problem solving and decision making skills
- Excellent interpersonal skills
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Skills Required
- Master's degree in Statistics or a related field and 3 or more years of industry experience, or equivalent
- Bachelor's degree in Statistics or a related field and 3 or more years of industry experience plus 4 or more years of SAS programming experience, or equivalent
- Proficiency with SAS programming
- Ability to organize multiple priorities
- Excellent communication and leadership skills
- Demonstrated problem-solving and decision-making skills
- Excellent interpersonal skills
What We Do
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
