Associate Director, Biostatistics – Orbis Clinical

Title of the Job: Associate Director, Biostatistics

Location: Washington DC

Job Description: The Associate Director, Biostatistics will be responsible for providing statistical expertise to all company studies, and is primarily responsible for the development of protocol and statistical analysis plan, data analysis, data presentation and report writing. S/he may also be responsible for providing mentorship to junior biostatisticians.Primary Responsibilities:

• Working as leading statistician on multiple studies/projects across different therapeutic areas. Contribute to clinical trial design, protocol development and Clinical Study Report (CSR)
• Participate study related activities and provide statistical consultation, input and guidance to cross-functional groups
• Develop and/or review statistical documents or deliverables for clinical trials including Statistical Analysis Plan (SAP) and integrated summaries of drug efficacy and safety, TFLs, interim analysis plan and others.
• Manage CRO statisticians and internal biostatistics team, including junior statistician, contract statistician and programming team in support of biostatistics operational activities.
• Work as biostatistics function representative in clinical projects and studies. Attend project and study team meetings as needed. Support and participate activities related to regulatory requests and meetings as needed. Close communication with functional manager is expected.
• Provide statistical expertise by identifying potential issues, providing recommendations and bring in statistical experts external for relevant issues as needed.

Compensation Details:

• The Pay Range for this position is $175,000 -$225,000. It is possible that this position can be hired outside of this salary range based on experience.

EEO and Reasonable Accommodation Statement:Orbis Clinical provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, housing, age, disability or genetics.We will consider all qualified applicants for employment, including those with criminal histories, in a manner consistent with the requirements of applicable federal, state, and local laws.By applying for this position, you agree that any calls from Orbis Clinical and its subsidiaries may be monitored or recorded for training and quality assurance purposes.Additional skills : -Ph.D. in Biostatistics or statistics -At least 4 years of pharmaceutical clinical trial experience -In-depth knowledge of clinical trials methodology, regulatory requirements, statistics -Comprehensive experience of SAS programming and R/S language

Company Name: Orbis Clinical

Salary:

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