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Sr. Principal Statistics Paramus, NJ
Job in
Paramus, Bergen County, New Jersey, 07653, USA
Listed on 2025-12-27
Listing for:
ESR Healthcare
Full Time
position Listed on 2025-12-27
Job specializations:
-
IT/Tech
Data Scientist, Data Analyst, Data Security
Job Description & How to Apply Below
Sr. Principal Statistics Paramus, NJ
Experience level:
Mid-senior
Experience required:6 Years
Education level:
Doctorate
Job function:
Management
Industry:Pharmaceuticals
Total position:1
Relocation assistance:
No
Visa sponsorship eligibility:
No
JOB DESCRIPTION:
- The Senior Manager in Statistics responsible for perform statistical activities in clinical trials from protocol development to final study report and statistical activities in drug in-licensing, regulatory filings and marketing.
RESPONSIBILITIES:
- Review protocol, understand study requirements, prepare statistical sections, design study elements including sample size calculation, analysis methods, study duration, etc.
- Review CRF, database design, and edit check specs
- Review study quality surveillance plan and monitor study conduct
- Prepare and/or review SAP, TFL shells and specifications for variable derivation
- Work closely with Statistical Programmers and Clinical Data Manager in identify data quality issues for key efficacy and safety variables
- Provide statistical and validation support for statistical analysis, analysis datasets and TFL Review study report, manuscripts and other documents related to statistics
- Work on responses to health authorities and execute new analysis required for responses, review statistical inputs for regulatory documents
- Perform other ad-hoc statistical activities as needed
- Works effectively with cross functional groups, study team, and vendors. Proactively control and monitor timelines related to statistics and statistical programming
- Participates in monitoring CRO activities and reviewing CRO deliverables
- Other duties as assigned
QUALIFICATIONS:
- 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
PHYSICAL AND MENTAL REQUIREMENTS:
- Ability to multitask
- Adapts to change
- Maintain composure under pressure
- Ability to follow verbal or written instructions and use of effective verbal communications
- Adapts change, adjust change and grasps information quickly
- Examine and observe details
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