Statistical Analyst (Experienced, SAS)

				Overview:

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

Responsibilities:

* Development of detailed Medpace Data Analysis Plan for assigned projects;
* Development of analysis databases;
* Communication of project requirements for CRF design, database design, and database clean-up to ensure the key study variables are suitable for analysis; 
* Programming of study analysis, review of study results, and preparation of statistical methods section for clinical/statistical reports, and related regulatory submission documents;
* Communication of statistical results to medical writing personnel to ensure accurate interpretation; and
* Collaboration with Global Statistics team members and programmers to ensure study outputs are produced to a high quality and in a timely fashion.

Qualifications:

* Master's Degree in statistics, biostatistics, or equivalent areas and strong relevant industry or equivalent experience;
* SAS Programming experience;
* Excellent communication and leadership skills;
* Familiarity with regulatory requirements/guidelines for data submission and analysis;
* Expertise in biostatistical methodologies applicable to Clinical Trials; and
* Knowledge of advanced programming methods.
			

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