NNIT

Senior Consultant – Regulatory Affairs (Life Sciences)

Fès-Meknès

CDI / Temps pleinHybride5–10 ansLicence / Bac+3Anglais, Allemand, Français, ItalienJuridiquePharmaceutique

L’essentiel du poste

Résumé par Postule AI

Senior Consultant role at NNIT, a leading life sciences consultancy, focused on Regulatory Affairs with emphasis on IDMP expertise. Requires 5+ years of regulatory affairs experience in pharma or consulting, bachelor's degree minimum, and strong technical skills in PMS, RIMS, and regulatory systems. Combines project delivery (75%), business development (10%), RFP management (10%), and mentoring (5%). Fluent English required; additional European languages desired. Based in UK or Europe with occasional travel.

Vos missions

  • Lead consultancy projects as advisor, project lead, or architect, managing client engagements and project delivery outcomes
  • Drive business development, pre-sales activities, and thought leadership initiatives to expand NNIT's market presence
  • Develop and deliver Requests for Proposal (RFPs) to secure new and expanded client projects
  • Coach and mentor junior consultants within the Regulatory Affairs team to build organizational capability
  • Manage relationships with clients, partners, and vendors while providing IDMP regulatory expertise

Profil recherché

  • You have 5+ years of proven regulatory affairs experience in pharma or consulting with demonstrated success
  • You possess deep IDMP expertise and stay current with EMA regulatory updates and requirements
  • You enjoy mentoring junior colleagues and contributing to business development alongside project delivery
  • You are fluent in English and interested in working in a multicultural European environment
  • You combine technical regulatory knowledge with strong client management and communication skills

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About the Role

Join NNIT's Regulatory Affairs team as a Senior Consultant, leading consultancy projects and driving business development in the life sciences sector. This role combines hands-on project delivery with strategic business growth and mentorship responsibilities.

Key Responsibilities

  • Lead consultancy projects (75% of time) in advisor, project lead, or architect roles, managing client engagements and project delivery
  • Contribute to business development, pre-sales, and thought leadership activities (10% of time)
  • Develop and deliver Requests for Proposal (RFPs) to secure new and expanded client projects (10% of time)
  • Coach and mentor junior consultants within the Regulatory Affairs team (5% of time)
  • Manage client, partner, and vendor relationships while expanding NNIT's client base
  • Provide expertise in IDMP regulatory affairs, including data transformation, PMS/RIMS systems, and EMA compliance

Essential Qualifications

  • Bachelor's degree in Pharmaceutical Compliance, Regulation, or related field (or equivalent with significant consulting/industry experience)
  • Significant experience in Regulatory Affairs within a pharmaceutical company or as a consultant
  • Proven consulting experience, ideally with a recognized life sciences consultancy
  • Demonstrated expertise in IDMP, including data transformation, PMS, RIMS, XEVMPD, and current EMA updates
  • Proficiency in PMS and Postman API
  • Excellent documentation, communication, and interpersonal skills
  • Fluency in oral and written English (required); German, Danish, Italian, or French (desired)

Preferred Qualifications

  • Master's degree in Pharmaceutical Compliance or Regulation
  • Regulatory experience within the pharmaceutical industry
  • Experience with Power BI applications
  • Python coding and scripting experience

What We Offer

  • Dynamic workplace with excellent working conditions, social activities, and work-life balance
  • Multicultural, friendly, and informal working environment
  • Competitive salary with bonus and benefits (home internet contribution, fitness funding, and more)
  • Opportunity to work with leading life sciences clients
  • Diverse project portfolio and career development opportunities
  • Personal development model supporting long-term career goals

Location: UK or Europe (travel <20% expected)

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