Kani Solutions Inc
Principal Statistician
⭐ - Featured Role | Apply direct with Data Freelance Hub
This role is for a Principal Statistician in Paramus, NJ, on a 6+ month contract, offering competitive pay. Requires a Ph.D. or MS in Statistics/Biostatistics, 4-6 years of pharmaceutical/CRO experience, and expertise in SAS, ICH guidelines, and CDISC standards.
🌎 - Country
United States
💱 - Currency
$ USD
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💰 - Day rate
Unknown
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🗓️ - Date
May 15, 2026
🕒 - Duration
More than 6 months
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🏝️ - Location
On-site
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📄 - Contract
Unknown
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🔒 - Security
Unknown
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📍 - Location detailed
Paramus, NJ
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🧠 - Skills detailed
#Leadership #Licensing #SAS #CDISC (Clinical Data Interchange Standards Consortium) #Statistics
Role description
Job Title: Sr Principal Statistics
Location: Paramus, NJ 07652 (Onsite)
Hire Type: Contract (6 months+)
Job Description:
The Senior Manager in Statistics will be responsible to perform statistical activities in clinical trials from protocol development to final study report and statistical activities in drug in-licensing, regulatory filings and marketing.
Required Skills:
• Education: Ph.D. or MS in Statistics or Biostatistics
• Minimum of 4 years (Ph. D) or 6 years (MS) Pharmaceutical/CRO industry experience
• Excellent knowledge of SAS computer package
• Excellent knowledge of industry standards, such as the ICH guidelines, CDISC data structures and FDA guidelines
• Excellent organizational skills, time management, and ability to meet established deadlines
• Excellent communication and interpersonal skills to effectively interface with others
• Exceptional interpersonal skills and problem-solving capabilities
• Ability to work independently and collaboratively
• Ability to provide leadership for the CRO statisticians and statistical programmers.
Job Title: Sr Principal Statistics
Location: Paramus, NJ 07652 (Onsite)
Hire Type: Contract (6 months+)
Job Description:
The Senior Manager in Statistics will be responsible to perform statistical activities in clinical trials from protocol development to final study report and statistical activities in drug in-licensing, regulatory filings and marketing.
Required Skills:
• Education: Ph.D. or MS in Statistics or Biostatistics
• Minimum of 4 years (Ph. D) or 6 years (MS) Pharmaceutical/CRO industry experience
• Excellent knowledge of SAS computer package
• Excellent knowledge of industry standards, such as the ICH guidelines, CDISC data structures and FDA guidelines
• Excellent organizational skills, time management, and ability to meet established deadlines
• Excellent communication and interpersonal skills to effectively interface with others
• Exceptional interpersonal skills and problem-solving capabilities
• Ability to work independently and collaboratively
• Ability to provide leadership for the CRO statisticians and statistical programmers.
