SENIOR DIGITAL REGULATORY CONSULTANT LIFE SCIENCES in London

CompanyA leading international organization specializing in consulting and digital solutions for the Life Sciences sector, with headquarters in Italy. Established in 2010, the company supports pharmaceutical and biotech organizations across regulatory affairs, pharmacovigilance, clinical trials, medical affairs, and quality assurance. It delivers innovative digital tools and high value-added services, with a strong focus on regulatory compliance and operational efficiency.

The RoleAs a Senior Digital Regulatory Consultant, you will act as a key point of contact for international clients, with responsibility for requirements analysis, technology solution design, implementation coordination, and change governance.

You will work closely with internal IT teams, developers, product specialists, and regulatory functions, ensuring alignment between client needs, regulatory compliance, and technical deliverables.

Key Responsibilities

Lead the design and implementation of digital regulatory systems (RIM, eCTD, IDMP, PV systems, Quality Systems)

Coordinate internal and external technical and functional teams, ensuring quality, timelines, and compliance with requirements

Translate regulatory requirements into implementable technical specifications

Analyze existing regulatory processes (submission management, labelling, safety, clinical) to identify inefficiencies, risks, and opportunities for digital transformation

Advise clients on technology architecture, digital tools, system integrations, and evolutionary roadmaps

Monitor KPIs, project progress, budgets, and the impact of implemented solutions

Contribute to the definition of the digital portfolio and the development of new, high-tech services

You Are the Ideal Candidate If You

Have at least 7–10 years of experience in the Life Sciences sector, in technical or digital/IT transformation roles

Have worked in regulatory affairs, pharmacovigilance, QA, or clinical environments, preferably within pharmaceutical, biotech, or CRO organizations

Hold a degree in Computer Science, Engineering, Bioengineering, Chemistry, or Pharmacy, with strong digital expertise

Have solid knowledge of RIM systems, eCTD, IDMP, digital platforms for regulatory and PV, API integrations, workflow automation, data governance, GxP, and EMA/FDA guidelines

Have at least 5 years of consulting experience, including client management and delivery of complex projects

The Company Offers

Permanent employment contract

Competitive salary and benefits package

Flexible working arrangements (full remote or hybrid options)

Collaboration with multidisciplinary teams on international projects

Opportunities to contribute to business growth and the development of the digital offering

All vacancies are open to candidates of all genders (Law 903/77).

To check whether this position is still open, please visit https://cpltaylor.it/annunci/#/ and enter the job reference code.

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