Senior Implementation Consultant – RIMS

🕒 il y a 5 mois

🇬🇧 Royaume-Uni – Télétravail

⏰ Temps Plein

🟠 Senior

🛠️ Spécialiste de l'Implémentation

🇬🇧 Parrain de Visa de Travailleur Qualifié UK

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👻 Score fantôme 18%

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🗣️🇩🇪 Allemand requis

🗣️🇪🇸 Espagnol requis

🗣️🇮🇹 Italien requis

🗣️🇺🇸🇬🇧 Anglais requis

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Logo of Veeva Systems

Veeva Systems

1001 - 5000 employés

🏥 Santé

💼 Conseil

📦 Logistique

Healthcare • Consulting • Logistics

Veeva Systems Inc. est un leader des logiciels cloud pour l’industrie mondiale des sciences de la vie. Animée par l’innovation, l’excellence produit et la réussite de ses clients, Veeva compte plus de 875 clients, des plus grands groupes pharmaceutiques aux biotechs émergentes. Le siège de Veeva est situé dans la région de la baie de San Francisco, avec des bureaux au Canada, en Europe, en Asie et en Amérique latine. Veeva vise 10 000 collaborateurs d’ici 2025 : consultez la section Offres d’emploi pour nos postes ouverts et notez que toute correspondance adressée aux nouveaux candidats ou aux candidats en cours ne proviendra que d’une adresse e‑mail officielle @veeva.com.

Description

• Lead software implementation projects at life sciences companies ranging from the world's largest pharmaceutical companies to emerging biotechs • Lead the solution design for implementation and use of the Vault Regulatory suite (Veeva Registrations, Veeva Submissions, Veeva Submissions Archive, Veeva Publishing) • Lead configuration requirements workshops, design, prototype, configure, and document content solutions • Program and project management, including resource planning, leading and motivating a cross-functional team • Primary customer liaison managing communication between the project team, customer, and internal stakeholders • Mentor project team and consultants, helping others improve their consulting skills

🎯 Exigences

• 8+ years experience performing system implementations for life sciences or healthcare companies, either as a consultant, business or IT representative • In-depth knowledge of drug development processes and regulatory submissions; including, Labeling, Submission Publishing and/or Viewing systems • Proven ability to collaborate and communicate excellently with diverse stakeholders and ensure delivery to a high degree of satisfaction • Influential; experience leading teams through hard decisions and negotiating compromises • Technical abilities and willingness to “roll up your sleeves” to design, configure and implement a RIM solution • Expert on life sciences compliance and computer systems validation requirements • Ability to work independently in a fast-paced environment • Ability to travel as required by the business

🏖️ Avantages

• Work Anywhere • Flexibility to work from home or in the office

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