Tfl

60 Tfl Jobs Hiring Near You

Bell Person

Stowe, VT · On-site

$17/hr

Ensure arriving and departing guests receive immediate attention through portage, door opening, parking and information about Stowe and TFL in particular. * Maintain awareness of current events and ...

Cut in-house TFL backs, ⅝" birch drawer boxes, flat base molding, and flat crown * Self-check every part you produce: wrong cuts, missed bores, and bad edges don't move forward * Show newer crew ...

Biostatistician

West Chester, PA · On-site

$70 - $98/hr

Author and review of statistical analysis plans, analysis dataset specifications, and TFL shells. * Work with programming and other cross-functional teams in Phase-4 non-interventional study to ...

Oversee and lead the vendor/CRO biostatistics and programming teams, including activities during TFL development, Data Monitoring Safety Board meetings, interim analyses, and database locks * Execute ...

Sr. Director, Biostatistics

Cambridge, MA · On-site

$270K - $290K/yr

Oversee and lead the vendor/CRO biostatistics and programming teams, including activities during TFL development, Data Monitoring Safety Board meetings, interim analyses, and database locks * Execute ...

Perform generation, validation and QC/QA of SDTM, ADam and TFL output in accordance with SOPs, SOIs, and guidance documents. * Create and maintain specifications as per SDTM/ADaM standard and study ...

Showing results 41-60

Tfl Jobs Information

Infographic showing various job openings at Tfl in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 80% Physical, and 20% Remote job distribution.

Senior Principal Statistical Programmer

Katalyst

Paramus, NJ • On-site

Full-time

Re-posted 2 days ago


Job description

Summary of Position:
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.
Duties and 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
Must have:
  • 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
  • Ability to work independently and problem-solve
  • Ability to provide leadership for the CRO statisticians and statistical programmers