Temp Biostatistician

Pay Range: $70.52 - $95.27/hr

Remote Role (US Only)

12 Month Contract

This position is for a qualified statistician/biostatistician to support Clinical Biostatistics within Global Development. The incumbent will work with cross-functional teams to articulate drug development questions, assess the feasibility of endpoints and frame statistical approaches to address those questions, design clinical experiments and interventional studies to generate and analyze the resulting data, and work with teams to appropriately interpret the results and make

decisions. The incumbent will co-author clinical study protocols, statistical analysis plans, and perform statistical analyses for interim and final reports. The incumbent will also develop and deliver training to non-statistical colleagues,

collaborate on development of new infrastructure and processes, and influence the external pharmaceutical industry and regulatory environment through participation in professional associations, conferences, and publications.

As a Temp Manager Biostatistician, a typical day may include:

Interacts with Medical Directors, Clinical Scientists, Regulatory Affairs, Preclinical scientists, Statistical Programming,

Data Management, Medical Writing, and others to design and analyze clinical trials.

Develops individual protocols and statistical analysis plans and determines appropriate statistical methodology for data analysis.

Collaborates with Statistical Programming on the programming of tables, figures and listings to support decision making and for regulatory reporting.

Evaluates appropriateness of available software for planned analyses and determines needs for use of novel statistical methodology or tools.

Analyzes data and interprets results from clinical trials and of data from non-trial sources to facilitate program-level decision making.

Prepares presentations and written reports to effectively communicate results to the project team, management, and regulatory agencies. Co-presents findings to management.

Is involved in research activities for innovative statistical methods and applications in clinical trial development as well as providing training to non-statisticians.

To be considered for this job, you must have the following:

PhD or equivalent degree in statistics/biostatistics with >2 years’ experience in the pharmaceutical industry

This is a contract position at Regeneron with Magnit Global being the Employer.

To do our best work we need different viewpoints.  Therefore, we celebrate diversity and embrace inclusion. As an equal opportunity employer, we are dedicated to building a team that represents a variety of backgrounds, perspectives, and skills.  We strive to ensure that we maintain a positive and enriching work environment for all.

W2 only, no third party solicitation