Biostatistician II (Clinical Trial Experience Required)

CTI; Covington (KY); Hybrid; USD 120,000 - 180,000; Full time

Benefits offered by this job

Hybrid work from home opportunities

Tuition reimbursement

Health benefits and paid vacation

Paid parental leave

Job summary

CTI Clinical Trial and Consulting Services seeks a Lead Biostatistician to guide studies, serve as primary statistical contact, and develop IAPs/SAPs, SDTM/ADaM datasets, and TLFs for analysis. You will contribute to RSS, CSRs, and publications with strong regulatory awareness.

The role requires 2+ years in pharma/CRO biostatistics, a Master’s degree, CDISC SDTM/ADaM experience, and ICH/GCP compliance. CTI offers hybrid work arrangements, competitive benefits, and a global collaboration

Qualifications

• 2 years of related biostatistics experience in pharma or CRO
• Master’s degree in Biostatistics, Statistics, or related field
• CDISC SDTM and ADaM mapping experience; regulatory knowledge

Responsibilities

• Serve as primary statistical contact for internal and external project team members
• Communicate and maintain project budgets and timelines with Biostatistics management
• Review case report forms (CRFs) and completion instructions
• Develop SDTM/ADaM dataset specifications and mock tables/figures (TLFs)
• Perform statistical analyses by programming derived datasets and TLFs and validate programs
• Develop/review statistical methods and results sections of reports, CSRs, or publications
• Assist in planning/designing clinical studies (design, endpoints, sample size, randomization)
• Follow CTI SOPs and GCP/ICH guidelines; maintain accurate records in eTMF

Skills

Biostatistics experience

Regulatory submissions experience

Communication of statistics

Education

Master’s degree in Biostatistics or related field

Tools

CDISC SDTM/ADaM mapping

Job description

What You'll Do:

• As the lead Biostatistician on the studies assigned, perform the following tasks:
  • Act as primary statistical contact for internal and external project team members.
  • Communicate and work with Biostatistics management to maintain the project budget and timelines.
  • Review case report forms (CRFs) and completion instructions
  • Give input to database design and data edit considerations necessary to collect and clean data
  • Develop, or assist in the development of, Interim Analysis Plans (IAPs) and Statistical Analysis Plans (SAPs) as needed per the protocol
  • Develop program specifications – SDTM and ADaM dataset specifications and mock tables, listings and figures (TLFs) – needed to perform the analysis defined in the IAP/SAP
  • Perform the statistical analysis by independently programming derived datasets and TLFs and validate the developer’s corresponding programs per department SOPs
  • Develop or review statistical methods and results sections of statistical reports, clinical study reports (CSRs), or publications
  • Assist in planning and designing clinical studies, including:
    • overall study design development
    • outcome / endpoint determination
    • power analysis / sample size estimation reports
    • randomization and blinding procedures development
    • statistical methods section development in the protocol
    • Develop, or assist in the development of, Randomization Plans and randomization programs or lists
• Carry out all activities according to CTI SOPs and project-specific conventions within the framework of Good Clinical Practice (GCP) / International Conference on Harmonization (ICH) guidelines
• Rely on instructions and Biostatistics SOPs to ensure timely, standard, and quality deliverables to customers
• Maintains accurate records of all work performed and ensure all relevant statistics documents are filed in the eTMF per the project-specific eTMF Plan

What You'll Bring:

• 2 years of related biostatistics experience in either a pharmaceutical or CRO environment or other relatable statistical experience
• Master’s degree in Biostatistics, Statistics, or related field
• CDISC SDTM and ADaM dataset mapping experience
• Knowledge of ICH guidelines and regulatory requirements as they relate to biostatistics activities
• Experience providing ability to explain complex statistical concepts to other project team members
• BLA/NDA Submission experience; regulatory representation (i.e., meeting preparation/attendance, follow-up with regulatory communication)
• Therapeutic experience in transplantation, autoimmune diseases, and kidney and liver disease

About CTI

CTI Clinical Trial and Consulting Services is a global, privately held, full‑service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development, from drug concept to commercialization. CTI is headquartered in the Greater Cincinnati, OH region with global operations in collaboration with pharmaceutical, biotechnology, and medical device firms. For more information, visit www.ctifacts.com

Why CTI?

• Advance Your Career – We support career progression through a structured mentoring program and leadership courses that provide the support needed to grow. We also value ongoing education and training through tuition reimbursement and a dedicated training department.
• Join an Award-Winning and Valued Team – We have an award‑winning unparalleled culture that can be felt by our employees across 60 countries. We support a work‑life balance and the importance of time with family by offering generous health benefits and vacation packages, hybrid work from home opportunities, and paid parental leave. We also encourage care for the world around us through our unique CTI Cares program.
• Make a Lasting Impact – We focus on moving medicine forward by working on treatments for chronically and critically‑ill patients, who depend on us to bring life‑changing therapies to market.

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