Senior Consultant, Life Sciences & Clinical Operations

Devote Consulting

Lisboa

Híbrido

EUR 55 000 - 75 000

Tempo integral

Há 10 dias
Gerador de candidaturas

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Resumo da oferta

Devote Consulting seeks a Senior Consultant with expertise in clinical operations, data, and GxP systems to help life sciences clients optimize processes and compliance documentation. You will deliver changes across R&D, clinical operations, and regulatory affairs, guiding projects in a fast-paced consulting environment.

You hold a master’s degree in business administration, IT, or life sciences, have 5+ years of regulated-industry consulting experience, and excel at stakeholder management and

Qualificações

  • A master's degree in business administration, IT, life sciences or equivalent.
  • 5+ years of experience as a consultant, business analyst, project manager, or equivalent in regulated industries such as Pharma, Biotech, or MedTech.
  • Proven analytical and problem-solving skills, with a passion for making an impact.
  • Experience in creating compliance and validation documentation.
  • Fluent in English, with excellent verbal and written communication skills.
  • Expertise in Clinical R&D systems (CTMS, eTMF, eSource, RBM, EDC, QMS, LIMS, etc.) and/or medical devices.

Responsabilidades

  • Deliver changes in life sciences processes, data and systems within R&D, clinical operations, and regulatory affairs.
  • Design and optimize business workflows for greater efficiency.
  • Lead project planning, change management, and delivery of compliance documentation.
  • Ensure project progress and maintain high-quality standards for deliverables.

Conhecimentos

Analytical thinking
Problem solving
English (fluent)

Formação académica

Master's degree in Business Administration, IT, Life Sciences or equivalent

Descrição da oferta de emprego

Devote Consulting seeks a Senior Consultant with expertise in clinical operations, data, and GxP systems to help life sciences clients optimize processes and compliance documentation. You will deliver changes across R&D, clinical operations, and regulatory affairs, guiding projects in a fast-paced consulting environment.

You hold a master’s degree in business administration, IT, or life sciences, have 5+ years of regulated-industry consulting experience, and excel at stakeholder management and

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