1

Stage En Audit Jobs (NOW HIRING)

The work sits at the architecture and design stage, where protection is layered into the system ... Own laser safety standards for the team across ANSI Z136, IEC and BS EN 60825, and JIS C 6802, and ...

The work sits at the architecture and design stage, where protection is layered into the system ... Own laser safety standards for the team across ANSI Z136, IEC and BS EN 60825, and JIS C 6802, and ...

Observability & Audit - a multi-pipeline telemetry architecture (operational + security ... Guardrails Runtime - a multi-stage safety pipeline (input moderation prompt-injection defense PII ...

... with PMO stage-gate requirements. * Manage variation orders, engineering changes, and baseline ... Ensure ERP, SharePoint, and PMO systems remain accurate, current, and audit-ready. * Prepare ...

Audit performance quality and build training plans for direct reports. Ensure staff is motivated ... stage. * Utilize Engineering skills and applicable codes and standards to implement electrical ...

Showing results 21-40

Stage En Audit information

See salary details

$11K

$90K

$140.5K

How much do stage en audit jobs pay per year?

As of Sep 11, 2026, the average yearly pay for stage en audit in the United States is $89,997.00, according to ZipRecruiter salary data. Most workers in this role earn between $48,000.00 and $130,000.00 per year, depending on experience, location, and employer.

What cities are hiring for Stage En Audit jobs?

Cities with the most Stage En Audit job openings:

What are popular job titles related to Stage En Audit jobs?

For Stage En Audit jobs, the most frequently searched job titles are:

Infographic showing various Stage En Audit job openings in the United States as of June 2026, with employment types broken down into 92% Full Time, 5% Part Time, 1% Temporary, and 2% Contract. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution, with an average salary of $89,997 per year, or $43.3 per hour.

Sr. Manager, Statistical Programming

Cambridge, MA โ€ข On-site

Other

Posted 24 days ago


Key responsibilities

  • Ensure the quality and timeliness of statistical programming deliveries for studies they lead.

  • Oversee programming preparation activities for global regulatory submissions and respond to health authority questions.

  • Contribute to the oversight of outsourced programming work to ensure quality, budget, and timeline compliance.


Job description

## Sr. Manager, Statistical ProgrammingApplylocations: Paris: Cambridge One Main: Londontime type: Full timeposted on: Posted 9 Days Agojob requisition id: R-21927**Title:**Sr. Manager, Statistical Programming**Company:**Ipsen Innovation (SAS)**About Ipsen:**Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology, Rare Disease and Neuroscience. Supported by nearly 100 years of development experience, with global hubs in the U.S., France and the U.K, we tackle areas of high unmet medical need through research and innovation. Our passionate teams in more than 40 countries are focused on what matters and endeavor every day to bring medicines to patients in 88 countries. We build a workplace that champions human-centric leadership and fosters a culture of collaboration, excellence and impact. At Ipsen, every individual is empowered to be their true selves, grow and thrive alongside the companyโ€™s success. Join us on our journey towards sustainable growth, creating real impact on patients and society!For more information, visit us at **https://www.ipsen.com/**and follow our latest news on **LinkedIn** and **Instagram**.**Job Description:****WHAT -** **Summary & Purpose of the Position**The Senior Manager is responsible to perform as a lead programmer on multiple compounds/studies within the Statistical Programming function to support Ipsenโ€™s Asset under a specific Therapeutic area (Oncology, Rare Disease, or Neuroscience). The role requires hands on and managerial and technical expertise to ensure the quality and timelines of statistical programming deliveries are met either by CRO oversight or through in house production.**WHAT -** **Main Responsibilities & Technical Competencies*** Ensure the quality and timeliness of all the deliveries (in house or outsourced) are met for the studies they lead;* Ensures consistency of process and executional excellence of services for the studies they lead;* Oversees programming preparation activities for global regulatory submissions and responding to health authority questions for the studies he/she leads;* Contributes to ensuring the oversight of all outsourced programming work to quality, budget, and timeline;* Ensures the quality of Statistical Programming deliverables, including tables, listings, figures, datasets, and associated documentation, e.g. DEFINE.XML. Participate in the development and implementation of SAS programming standards, SOPs and work instructions, including program validation and documentation;* Ensures their study related documentation according to Ipsen processes and in a ready state acceptable for audit;* Looks for opportunities to continually improve ways of working, adapt to/ adopt cutting edge approaches and manage programming needs for evolving and complex study design methodologies.**HOW - Behavioural Competencies Required*** Collaborates and communicates without boundaries, continuously removes organizational barriers;* Seeks relevant stakeholder views/expertise and coaches/ensures decisions are made by consent vs. consensus;* Takes personal accountability for decisions, actions, successes and failures, and fosters the same for others;* Plans and aligns effectively (steps, resources, timelines etc.);* Approaches priority setting and setting the stage through the lens of execution;**HOW - Knowledge & Experience**Knowledge & Experience (essential):* Proficiency in statistical programming package(s), SAS is required;* Familiar with Global Clinical Data Interchange Standards Consortium (CDISC);* Experience in SDTM and ADaM specification and programming;* Experience in reporting and TFL programming.* 8+ yearsโ€™ programming experience in pharmaceutical/biotech/CRO environment in drug discovery/clinical trials / drug developmentKnowledge & Experience (preferred):* R or other packages are desired;* Understand clinical data flow. Experience in NDA/sNDA submission is desired.Education / Certifications (essential):* Bachelor or MSc in Statistics, Mathematics, or Scientific DisciplineLanguage(s) (essential):* EnglishLanguage(s) (preferred):* FrenchNous nous engageons ร  crรฉer un lieu de travail oรน chacun se sent รฉcoutรฉ, valorisรฉ et soutenu, oรน nous incarnons ยซ The Real Us\*ยป. La valeur que nous accordons aux diffรฉrentes perspectives et expรฉriences motive notre engagement en faveur de l'inclusion et de l'รฉgalitรฉ des chances. Lorsque nous intรฉgrons des modes de pensรฉe diversifiรฉs, nous prenons des dรฉcisions plus rรฉflรฉchies et dรฉcouvrons des solutions plus innovantes. Ensemble, nous nous efforรงons de mieux comprendre les communautรฉs que nous servons. Cela signifie que nous voulons รฉgalement vous aider ร  donner le meilleur de vous-mรชme lorsque vous postulez ร  un poste chez nous. Si vous avez besoin d'amรฉnagements ou d'aide pendant le processus de candidature, veuillez en informer l'รฉquipe de recrutement. Ces informations seront traitรฉes avec soin et n'auront aucune incidence sur le rรฉsultat de votre candidature. \*Soyons nous-mรชme #J-18808-Ljbffr