Person2Person, LLC
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| Biostatistical Programer Based in Northern, NJ |
| Outstanding Contract opportunity with a global pharmaceutical Company focused on multiple therapeutic areas including Neurology, Oncology and Critical Care. They continue to move forward with an entry into biologics with the development of therapeutic antibodies and other such agents, which contributes to their innovate drug discovery process. Be a part of this global market leader! |
| SCOPE & DUTIES |
• Review protocols, statistical analysis plans and case report forms, and provide SAS data specifications
for clinical trials
• Ensure programming deliverables are consistent and comply with study protocols, statistical analysis
plans and case report forms
• Work under the supervision of project statistician to coordinate with data management and clinical
operation to ensure quality of clinical trial databases
• Develop standard programs to facilitate general programming requirement in clinical trials
• Provide ad-hoc analysis programming to explore repository databases and to support publications
• Ensure implementation of corporate standardized programming conventions and working guidance
for clinical trials
• Ensure programming deliverables are consistent and comply with study protocols, statistical analysis
plans and case report forms
• Work under the supervision of project statistician to coordinate with data management and clinical
operation to ensure quality of clinical trial databases
• Develop standard programs to facilitate general programming requirement in clinical trials
• Provide ad-hoc analysis programming to explore repository databases and to support publications
• Ensure implementation of corporate standardized programming conventions and working guidance
| REQUIREMENTS |
Master’s or equivalent degree in Biostatistics, Statistics, Epidemiology, Mathematics, Computer Science,
Life Sciences or related field
• 5+ years of pharmaceutical experience
• Good interpersonal, communication, problem solving, and analytical skills
• Work independently with minimum or none supervision
• Ability to collaborate and communicate with cross-functional team members
• Flexible and excellent ability to work on multiple studies with competing priorities
• Expert technical skills in SAS Base/Macro/Graph/Stat
• Excellent knowledge of CDISC-compliant SAS data structures and other related regulatory guidance
Life Sciences or related field
• 5+ years of pharmaceutical experience
• Good interpersonal, communication, problem solving, and analytical skills
• Work independently with minimum or none supervision
• Ability to collaborate and communicate with cross-functional team members
• Flexible and excellent ability to work on multiple studies with competing priorities
• Expert technical skills in SAS Base/Macro/Graph/Stat
• Excellent knowledge of CDISC-compliant SAS data structures and other related regulatory guidance
| Executive Recruiting Specialists in the NY/NJ/CT Region |
Apply today! For immediate consideration, please email resume to: lsydor@person2personllc.com |