Why RTI
About the Hiring Group
What You'll Do
What You'll Need
EEO & Pay Equity Statements
Equal Pay Act Minimum/Range
$125,000 - $153,000
RTI International is an independent, scientific research institute dedicated to improving the human condition. Our vision is to address the world's most critical problems with technical and science-based solutions in pursuit of a better future. Clients rely on us to answer questions that demand an objective and multidisciplinary approach—one that integrates expertise across social, statistical, data, and laboratory sciences, engineering, and other technical disciplines to solve the world’s most challenging problems.
We believe in the promise of science and technical solutions, and we push ourselves every day to deliver on that promise for the good of people, communities, and businesses in the US and around the world. If you are looking for the opportunity to make a real difference, RTI is the place for you.
About the Hiring Group
RTI International, is an independent nonprofit research institute dedicated to improving the human condition, is seeking a Contract Senior Clinical Trial Statistician (Sr. Stat) who is a strategic and hands-on leader responsible for overseeing end-to-end analysis activities across multiple clinical trials. This role ensures the integrity, accuracy, and completeness of clinical trial data in compliance with Good Clinical Practice (GCP), regulatory guidelines, and company standard operating procedures (SOPs). The Sr. Stat serves as the primary liaison between internal teams, contract research organizations (CROs)/external vendors, providing oversight, guidance, and innovation in all aspects of statistical analysis. This role plays a critical part in accelerating timelines, supporting regulated clinical trials, and driving the overall success of clinical development programs.
This is a 6-month contract position with the potential for extension or transition to regular employment.
What You'll Do
Study Leadership & Strategy
- Act as the lead trial statistician and provide the associated expertise for assigned Phase II/III trials, ensuring timely delivery of high-quality, submission-ready analyses.
- In collaboration with trial coordinators, investigators, and data managers, provide strategic input into study designs, sample size calculations, protocol development and implementation, data collection strategies, and analytic plans to optimize trial quality and efficiency.
- Ability to oversee and perform work to author, maintain, and implement study-level statistical analysis plans, analysis dataset specifications and TLF shells, randomization approaches, analysis and reporting programs, and other analysis-related deliverables and activities.
- Drive continuous alignment of analysis strategy with overall program milestones and regulatory objectives.
- Ability to translate clients’ needs into statistical practice.
Data & Analysis Quality, Oversight & Delivery
- Collaborates with data management to ensure accuracy, consistency, and completeness of trial data through ongoing review, cleaning, and reconciliation (SAE, labs, imaging, biomarkers, PK, PRO/ePRO, etc.).
- Ability to oversee and perform work to support operational reporting (e.g., sponsor/leadership status reports, DSMB reports, operational support reports).
- Coordinate and oversee interim and final analyses, collaborating on timing of database snapshots and ensuring data and analysis integrity for study monitoring, publications, and regulatory filings.
- Champion and help design and implement risk-based monitoring (RBQM) and centralized data review.
- Ability to oversee and perform work involved in adoption of CDISC standards (SDTM/ADaM) in analysis dataset creation.
Cross-Functional & Regulatory Support
- Routinely collaborate and liaise with Clinical Operations, Programming, Data Management, Medical Monitoring, and Safety throughout trial development and implementation to ensure alignment of analytic deliverables with trial and submission objectives.
- In collaboration with Clinical Operations and Data Management, design and develop data driven clinical trial surveillance reports to ensure quality of data at the trial and site level.
- In collaboration with Clinical Operations and Data Management, ensure data collection, completion and cleaning occurs per expected timelines and support escalation and resolution of identified issues.
- Collaborate with Clinical Operations, Data Managers, and Medical Monitors in pharmacovigilance data management and regulatory reporting.
- Deliver high-quality analytic results, datasets, listings, and reports to support regulatory submissions and health authority inspections.
- Collaborate on clinical study reports (CSRs), publications, and scientific presentations, ensuring analytic interpretation accuracy and consistency.
CRO & Vendor Management
- Provide oversight, governance, and quality management of CRO analytic deliverables, holding vendors accountable to timelines, budget, and quality.
- Review and approve vendor specifications and resulting deliverables.
- Proactively identify and escalate risks, implementing corrective actions to ensure successful partnership and delivery.
What You'll Need
Education & Experience
- Master’s degree in Statistics, Data Science, Mathematics, or a related field and minimum of 6 years of progressive experience in clinical trial analysis within a biotech, pharmaceutical, or CRO environment for trials conducted under INDs or equivalent experience. Equivalent experience is defined as a Bachelor’s degree and 8 years of experience.;
- Proven track record of leading statistical aspects of Phase II/III clinical trials through development, database lock, and reporting/submission.
- Deep understanding of ICH-GCP, FDA, EMA, and other global regulatory requirements, including expertise in design/analysis, CDISC standards (SDTM, ADaM), and associated electronic data submission to regulatory agencies.
- Strong leadership and project management skills, with the ability to manage multiple priorities in fast-paced environments.
- Exceptional problem-solving and analytical ability, with a focus on data integrity and risk management.
- Skilled communicator, able to influence and collaborate across cross-functional teams and with external partners.
- Able to lead meetings with both internal and external collaborators and communicate complex statistical concepts to both researchers and lay audiences.
- Vendor/CRO oversight experience.
- Technical proficiency in R is required. Additional proficiency in SAS, Python, or other data programming preferred.
- Demonstrated ability to work independently, exercise judgment, and drive outcomes with minimal supervision.
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EEO & Pay Equity Statements
For San Francisco, CA USA Job Postings Only: Pursuant to the San Francisco Fair Chance Ordinance, we will consider for employment qualified applicants with arrest and conviction records. Further information is available here.
RTI accepts applications to our job openings from candidates with criminal histories or conviction records in accordance with all applicable laws, including the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.
For Applicants in Massachusetts Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
The anticipated pay range for this role is listed below. Our pay ranges represent national averages and may vary by location as a geographic differential may be applied to some locations within the United States. RTI considers multiple factors when making an offer including, for example: established salary range, internal budget, business needs, and education and years of work experience possessed by the applicant. Further, salary is merely one element to our offer.
At RTI, we demonstrate our commitment to rewarding individual and team achievement through a total rewards package. This package includes (among other things) a competitive base salary, a generous paid time off policy, merit based annual increases, bonus opportunities and a robust recognition program. Other benefits include a competitive range of insurance plans (including health, dental, life, and short-term and long-term disability), access to a retirement savings program such as a 401(k) plan, paid parental leave for all parents, financial assistance with adoption expenses or infertility treatments, financial reimbursement for education and developmental opportunities, an employee assistance program, and numerous other offerings to support a healthy work-life balance.
Equal Pay Act Minimum/Range
$125,000 - $153,000
Master's degree in Statistics, Data Science, Mathematics or related field with 6+ years clinical trial analysis experience (or Bachelor's with 8 years); proven leadership in Phase II/III trials; ICH-GCP, FDA, EMA, CDISC standards; R proficiency required; vendor oversight experience.
Key Responsibilities
- leading statistical analyses
- overseeing trial data
- managing CRO vendors
Skills & Tools
R, SAS, Python
Job Details
- Category: Data and Analytics
- Seniority: Senior Level
- Commitment: Contract
- Workplace: Remote — United States
- Salary: USD 125,000 – 153,000 / year
- Languages: English
Benefits
- Generous paid time off
- Tuition reimbursement
- Retirement plan
- Generous parental leave
About RTI International
An independent nonprofit research institute dedicated to improving the human condition through science and technical solutions. — Industry: Research and Development