Statistical Analyst II

HI ,

This is Gayatri, a senior recruiter at Experis IT Manpower Group. Our client, the largest pharmaceutical industry, is seeking a Statistical Analyst II  to join their team.
 
Job Details

Job title: Statistical Analyst II
Location: Columbus , OH
Pay rate: $30-$32/hr. on W2
 

Must have the correct level of degree and years of experience required

Skills: Familiar with a variety of the field's concepts, practices, and procedures. A wide degree of creativity and latitude is expected.

Education: 

Bachelor's degree in Statistics with at least 3 years of experience OR Master's degree in Statistics with at least 1 year of experience OR PhD in Statistics or related field with no prior experience.

Experience with machine learning and/or big data analytics preferred. Experience with early discovery analytics and/or clinical trials is required.

Minimum master’s degree in Statistics or equivalent

Must be proficient in SAS, R or both.

Duties: 

Analyzes and interprets data from various sources. 

Compiles reports, charts, and tables based on established statistical methods. 

Relies on extensive experience and judgment to plan and accomplish goals. 

Performs a variety of tasks. Typically reports to a supervisor or manager.
Designs, plans and executes bioscientific components of plans for research and development and/or exploratory projects that establish the conditions essential for determining safety, efficacy, and marketability of pharmaceutical and/or biological products. Uses sound scientific methodology to conduct studies relating to the life processes of immunoassay, chemiluminescence, antibodies, animals, and humans. In development-phase projects, prepares the scientific component of protocols and which meet project objectives, health authority guidelines, and clinical trial methodology standards. Develops and/or applies scientific and mathematical bioresearch theories, advanced analytics, methods, and software. Organizes and interprets medical outcomes and results into tabular forms and is responsible for the scientific and mathematical component of reports describing studies, outcomes and methods used. Provides specifications and directions to the clinical programmers. May partner in program design and in establishing standards for clinical conduct, and the collection, management and/or reporting of medical research results.