Senior Manager, Statistical Programming in England

Senior Manager, Statistical Programming in England

England Full-Time 60000 - 80000 £ / year (est.) No working from home possible
Ipsen

At a Glance

  • Tasks: Lead statistical programming for innovative biopharmaceutical studies in Oncology, Rare Disease, or Neuroscience.
  • Company: Ipsen, a global biopharmaceutical company focused on transformative medicines.
  • Benefits: Empowering workplace culture, opportunities for growth, and impactful work on patient health.
  • Other info: Join a diverse team committed to innovation and inclusion.
  • Why this job: Make a real difference in patients' lives while advancing your career in a dynamic environment.
  • Qualifications: 8+ years in statistical programming, proficiency in SAS, and experience in clinical trials.

The predicted salary is between 60000 - 80000 £ per year.

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 endeavour 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 company’s success. Join us on our journey towards sustainable growth, creating real impact on patients and society!

Job Description 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 Ipsen’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.

Main Responsibilities & Technical Competencies

  • Ensure the quality and timeliness of all the deliveries (in house or outsourced) are met for the studies they lead;
  • Ensure consistency of process and executional excellence of services for the studies they lead;
  • Oversee programming preparation activities for global regulatory submissions and responding to health authority questions for the studies he/she leads;
  • Contribute to ensuring the oversight of all outsourced programming work to quality, budget, and timeline;
  • Ensure 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;
  • Ensure their study related documentation according to Ipsen processes and in a ready state acceptable for audit;
  • Look 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.

Behavioural Competencies

  • Collaborate and communicate without boundaries, continuously remove organizational barriers;
  • Seek relevant stakeholder views/expertise and coach/ensure decisions are made by consent vs. consensus;
  • Takes personal accountability for decisions, actions, successes and failures, and fosters the same for others;
  • Plan and align effectively (steps, resources, timelines etc.);
  • Approach priority setting and setting the stage through the lens of execution;

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+ years’ programming experience in pharmaceutical/biotech/CRO environment in drug discovery/clinical trials / drug development.

Knowledge & 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 Discipline.

Language(s) (Essential)

  • English.

Language(s) (Preferred)

  • French.

EEO Statement

Nous nous engageons à créer un lieu de travail où chacun se sent écouté, valorisé et soutenu, où nous incarnons « The Real Us». La valeur que nous accordons aux différentes perspectives et expériences motive notre engagement en faveur de l'inclusion et de l'égalité des chances. Lorsque nous intégrons des modes de pensée diversifiés, nous prenons des décisions plus réfléchies et découvrons des solutions plus innovantes. Ensemble, nous nous efforçons de mieux comprendre les communautés que nous servons. Cela signifie que nous voulons également vous aider à donner le meilleur de vous-même lorsque vous postulez à un poste chez nous. Si vous avez besoin d'aménagements ou d'aide pendant le processus de candidature, veuillez en informer l'équipe de recrutement. Ces informations seront traitées avec soin et n'auront aucune incidence sur le résultat de votre candidature.

Senior Manager, Statistical Programming in England employer: Ipsen

Ipsen in Wrexham is an excellent employer, offering a collaborative work culture that prioritises innovation and excellence. Employees benefit from a supportive environment with opportunities for professional growth, all while working in a state-of-the-art packing facility that operates on a convenient Monday to Friday schedule. Join us to be part of a team that values your expertise and contributions in mechanical engineering and vision systems.

Ipsen

Contact Details:

Ipsen Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Senior Manager, Statistical Programming in England

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We think you need these skills to ace Senior Manager, Statistical Programming in England

SAS Programming
Statistical Programming
CDISC Standards
SDTM and ADaM Specification
TFL Programming
Regulatory Submissions
Programming Standards Development

Some tips for your application 🫡

Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Ipsen!

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How to prepare for a job interview at Ipsen

Understand the Science

Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Ipsen that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.

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If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.

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