Full-Time
Senior Biostatistician
Integrated Resources
501-1,000 employees
No salary listed
Paramus, NJ, USA
In Person
Category
 Biology & Biotech (2) |
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Required Skills
SAS
biostatistics
Requirements
- Must have a MS in Biostatistics/Statistics with at least 10-12 years of experience or a PhD in Biostatistics/Statistics with at least 6 years of experience in the pharmaceutical, CRO or biotech industry.
- Strong SAS programming skills. – At least 3-5 years.
- Oncology experience is highly preferred.
- Good technical writing skills.
- Good communication skills (verbal and written).
- Strong teamwork ability/commitment and individual initiative.
- Strong organizational skills with ability to effectively manage multiple projects.
- We need is an experienced statistician who can do SAS programming at the same time can clearly interpret statistical concept and results to non-statisticians and key medical opinion leaders
Responsibilities
- Work closely with clinicians, programmers, and publication managers to generate and QC outputs for publications; review publication (abstract/manuscripts) to ensure accuracy, quality and soundness of statistical methodologies; coordinate internal resource utilization for publication and generate activities metrics for management review.
- Work with the clinical study team on study design, development and/or review of clinical study protocols.
- Develop and/or review statistical analysis plans, including Table/listing/figure shells, and final study report for clinical studies; perform post-hoc statistical analyses as needed.
- Work with the project statistician and clinical data managers on design/review of case report form, data transfer specification, edit check specification, and participation in user acceptance testing (UAT); generate/review data tables/listings and coordinate data review meetings during the course of the study to ensure data quality.
- Oversee CRO programming activities, perform quality assurance checks on internally or externally produced SAS tables, listings, and figures, and ensure the quality of CRO deliverables.
- May work with the Health Outcome team on the design/analysis/validation of projects.
- May work on submission teams as a statistician and/or a programmer.
- Act as lead Statistician on complex trials and across multiple studies.
- Act as a lead representative of the of the biostatistics department on project teams.
Desired Qualifications
- Oncology experience is highly preferred
Company Size
501-1,000
Company Stage
N/A
Total Funding
N/A
Headquarters
Edison, New Jersey
Founded
1996
Simplify's Take
What believers are saying
- Certification boosts appeal to quality-focused healthcare organizations.
- Reskilling programs cut time-to-hire amid workforce shortages.
- Positions IRI among 15,000 Joint Commission-accredited elite firms.
What critics are saying
- Certification lapses in 12-18 months from failed onsite review.
- Patient complaints trigger decertification and client losses in 6-12 months.
- AMN Healthcare captures IRI's mid-sized clients in 12-24 months.
What makes Integrated Resources unique
- Joint Commission Gold Seal certifies IRI's staffing compliance since 2009.
- AI tool Nova hybridizes with reskilling to close healthcare skills gaps.
- Focuses on diversity hiring and performance monitoring for elite placements.
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Benefits
Wellness Program
Mental Health Support
Flexible Work Hours
Phone/Internet Stipend
Home Office Stipend
Conference Attendance Budget
Company News
Integrated Resources, Inc.
Jan 3rd, 2024
Edison, New Jersey - Integrated Resources Inc. has earned The Joint Commission's Gold Seal of Approval(R) for Health Care Staffing Services Certification by demonstrating continuous compliance with its performance standards.
Integrated Resources, Inc.
Feb 1st, 2023
Integrated Resources Inc. has earned The Joint Commission’s Gold Seal of Approval ® for Health Care Staffing Services Certification by demonstrating continuous compliance with its performance standards.