Senior Statistical Programming Lead - Trials & Submissions
Ipsen Group
Ipsen Innovation is seeking a Sr. Manager, Statistical Programming to lead programming on multiple compounds/studies within Oncology, Rare Disease, or Neuroscience. The role combines hands-on SAS work with leadership to ensure quality and timely results for global regulatory submissions. The ideal candidate has 8+ years in pharmaceutical/biotech CRO environments, familiarity with CDISC standards, SDTM/ADaM, and strong reporting skills. English required; French language knowledge is a plus. #J-18808-Ljbffr Ipsen Group
- Alnylam Pharmaceuticals seeks an Associate Director, Statistical Programming to lead programming activities for clinical trials and NDA submissions. You will ensure SAS programs are developed, validated, and aligned with ICH and regulatory requirements. Role requires SAS...Senior
- ...Inc. is seeking an Associate Director, Statistical Programming to lead and contribute to statistical programming and analysis of clinical trial data. This role ensures quality and... ...ADaM standards, and support regulatory submissions (FDA/EMA). Travel is periodic; hybrid...Suggested
- Regeneron is seeking a Manager, Statistical Programming to join our Statistical Programming team, supporting a study from initial analysis through... ..., NJ or Cambridge, MA with an onsite work model. You will lead the development and QC of tables, listings, and graphs, manage...Senior
- ...expertise in biostatistics, data management, and regulatory submissions. This role focuses on statistical design, analysis, and CDISC-compliant reporting for diverse clinical trials. The candidate will lead SAS programming efforts, collaborate with protocol design teams, and...Senior
- ...Vor Biopharma seeks a Senior Manager of Statistical Programming to lead SAS programming efforts for clinical studies evaluating an autoimmune disease... ...quality, consistency, and timely completion of clinical trial submissions Requirements Advanced experience in clinical...Senior
$128.6k - $210k
Regeneron in Cambridge, Massachusetts is seeking a Manager to lead programming efforts for clinical studies. This role involves managing all programming deliverables, ensuring quality support for analysis, and overseeing documentation in a regulated environment. The ideal...Senior- A biotechnology company in Cambridge, MA is looking for a Senior Director of Biostatistics to lead statistical activities for clinical programs, provide input during regulatory submissions, and mentor junior statisticians. This role demands expertise in statistical analysis...Senior
$190k - $205k
...functions and geographies. Senior Manager, Statistical Programming The Senior Manager,... ...report, and submit clinical trial data. The Senior Manager will serve as lead programmer for assigned studies... .... Support regulatory submissions through preparation and validation...SeniorWorldwideFlexible hours$195k - $255k
...collaborate with leading academics in our... ...firm).About the Senior Biostatistician Position... ...regulatory submissions in a pharmaceutical... ...contributing statistical expertise to a major... ...advising on clinical trial design, analysis... ...Develop tools, programming standards, and...SeniorWork experience placementWork at officeLocal areaVisa sponsorship$132k - $172k
...our vision of becoming a leading biopharmaceutical company... ...Position Summary: The Senior Manager, Statistical Programming will work closely with... ...progress reports, electronic submissions and other internal and... ...for phase I-IV clinical trials in a pharmaceutical/CRO environment...SeniorTemporary workFor contractorsRemote work$136.96k - $205.44k
...Summary:The Principal Statistical Programmer works... ...the role of project lead Statistical... ...dataSolves complex clinical trial reporting problems... ...providing data and submission-related activities, often at Senior Management... ...educational assistance programs including student loan...Full timeWork experience placementSummer workWork at officeRemote workFlexible hours2 days per week- Sanofi in Cambridge, MA is seeking a Statistical Project Leader to steer statistical leadership for one or more late-phase rare disease projects. You will guide trial design, analysis plans, and regulatory interactions, while mentoring junior statisticians and collaborating...
$206.25k - $297.92k
Job title: Senior Director, Americas Region Lead, Diversity & Inclusion in Clinical Trials (DICT)Location: Morristown, NJAbout the jobJoin our Global Diversity & Inclusion... ...to monitor diversity KPIs and drive program-level accountability.Partnership & Stakeholder...SeniorFull timeLocal area- ...Coordinator for a nationwide Alzheimer's platform trial within the McCance Center. You will serve as the Center’s regulatory expert, leading regulatory risk management, planning, and... ...operations for the clinical trial program. Working closely with leadership, investigators...Senior
$142.16k - $213.24k
...professional disciplinary areas. Leads and directs a team of... ...negotiate internally, often at a senior level. Some external communication... ...(e.g., Lean, reengineering programs), or in a senior operations,... ...such as Mathematics, Statistics, Quantitative Finance, Economics...SeniorFull timeTemporary work$150.5k - $245.5k
...Regeneron seeks a Senior Manager of Statistical Programming to lead clinical programming teams across multiple studies from trial through regulatory submission and product launch. The role combines technical expertise in SAS programming with people management, mentoring...Senior$109.9k - $179.3k
...Responsibilities Lead or support programming and quality control of analysis datasets, tables, listings... ...Support creation and validation of submission requirements including annotated... ...support for presentations and statistical ad hoc requests Coordinate activities...- ...Writer (equivalent to Associate Director) to lead medical writing on multi-disciplinary... ...contract writers on the clinical program. You will develop key clinical documents... ...functions to ensure timely, high-quality submissions. #J-18808-Ljbffr Alnylam PharmaceuticalsSeniorContract work
$150.5k - $245.5k
...serious diseases. We are seeking a Senior Manager, Statistical Programming to join our Statistical Programming... ...and outputs in support of regulatory submissions Mentor others on the use of... ..., and information retention Enjoy leading programming work independently while...SeniorShift work$136.4k - $253.2k
...Science is recognized as a leading hub for top industry talent... ...exploratory analyses, and align statistical programming practices across both early... ...Program Lead serves as a senior leader within the... ...milestones and health authority submissions. In addition to overseeing...Full timeLocal area- ## Sr. Manager, Statistical ProgrammingApplylocations... ..., Statistical Programming**Company:**Ipsen... ...Position**The Senior Manager is responsible... ...to perform as a lead programmer on... ...global regulatory submissions and responding to... .../clinical trials / drug developmentKnowledge...Senior
$109.9k - $179.3k
...Regeneron seeks a Principal Statistical Programmer to lead clinical trial data programming and quality control activities supporting regulatory submissions and study launches. The role involves designing analysis datasets, specifications, and validation documents while...- Regeneron is seeking a Senior Manager of Statistical Programming to lead programming deliverables across a therapeutic portfolio. You will oversee analysis... ..., CROs, and internal partners to drive regulatory submissions and launches. The position is onsite in Warren, NJ or...
$155k - $225k
...establishing the leading, fully integrated... ...of base editing programs. Beam is a values... ...Beam is seeking a Senior Manager/Associate... ...Biostatistics to support the statistical design, execution... ...of clinical trials across Beam’s... ...regulatory submissions and responses to...SeniorFull time$126k - $234k
...at Novartis. A dynamic group of Clinical Trial Leaders (Clinical Scientists) who plan and... ...member of our team, you will support or lead the clinical science and operations of planning... ...data reviewContribute to project/program level plansMay mentor junior team membersSupport...SeniorFull timeWorldwide$90k - $135k
...Rhythm is seeking a Senior Statistical Programmer to join our... ...Biostatistics and Statistical Programming team. This role will... ...studies, regulatory submissions, and cross-functional... ...and Duties Lead or support statistical... ...of clinical trial reporting and regulatory...SeniorWork at office- ...The Biostatistics, Senior Manager is... ...responsible for providing statistical support for early... ...phase clinical trials in the Oncology... ...project objectives Lead and be... ...trials and regulatory submissions. Statistical leadership... ...statistical programming skills (SAS and/or...SeniorFull time
$150.5k - $245.5k
...diseases. We are seeking a Senior Manager, Statistical Programming to join our Statistical... ...Discover your role: Lead programming support across... ...guide programmers Lead submission-ready programming... ...— preferably in clinical trial data within biotechnology,...SeniorWorldwide- ...Biometrics, you will lead the quantitative disciplines... ...own Biostatistics, Statistical Programming and Data Science... ...statistical judgement to trial design, endpoints,... .... Serve as Hemab’s senior statistical voice with... ...regulatory interactions and submissions and representing our...
- ...experienced, hands‑on Senior Biostatistician for... ...who owns the statistical thinking on a trial end to end, from design... ...bear on real clinical programs. What You’ll Do... ...having personally led a submission High autonomy and... ...and engineers from leading pharma and top tech,...Senior
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