Medizin und Pharma

Freelance Digital Lead for Medical Platforms (m/f/d)

Remote,  Spanien60% RemoteFreiberuflichStart 1/2026Dauer 6 Monate100% Auslastung
Eingestellt von
Aristo Group
Ansprechpartner
Aneta Strzelecka
Projekt-ID
2942309
21 CfrProzessoptimierungComplianceVertragsmanagementDigitale TechnologiePharmakovigilanzSteuerungMedizinische VersorgungTechnologiestrategienVerhandlungQualitätsmanagementRegulatorischen AnforderungenRessourcenallokationService ManagementStakeholder ManagementWeb-PlattformenAris SoftwareDatenanalytikDigitalstrategieProjektlieferungRegulatory AffairsMedizinische AngelegenheitenSicherheitsbestimmungen

Beschreibung

Job title: Freelance Digital Lead for Medical Platforms (m/f/d)
Start of project: 01.01.2026
Duration of the project : 6 months
Project volume: approx. 1.020 hours
Location: Remote

Tasks:
  1. Serve as the central liaison between scientific, medical, regulatory, and safety functions and technology providers, including the establishment of governance frameworks for digital solutions.
  2. Develop and execute a comprehensive digital strategy across medical, regulatory, and safety domains.
  3. Lead the assessment, design, and development of scalable, compliant, and efficient technology solutions.
  4. Build and lead a cross-functional team of digital specialists, fostering innovation and high-quality delivery.
  5. Oversee the execution of the digital technology roadmap, ensuring delivery of required development and validation documentation.
  6. Drive the enhancement and optimization of core digital platforms used across medical, regulatory, and safety operations.
  7. Collaborate closely with relevant stakeholders to ensure alignment and seamless integration of digital initiatives.
  8. Manage application operations and ensure high-quality service management throughout daily and scheduled activities.
  9. Oversee vendor and service provider relationships in line with defined quality and performance expectations.
  10. Utilize data analytics to inform decision-making and support continuous improvement of processes.
  11. Ensure compliance of digital platforms and processes with applicable regulatory and quality standards.
  12. Manage budgets for digital initiatives and optimize resource allocation.
  13. Ensure that digital solutions are developed and maintained in accordance with required compliance and validation standards, without referencing specific systems or platforms.
Qualifications:
  1. 10+ years of experience in digital leadership roles within the life sciences or consumer healthcare sector.
  2. Proven background in implementing and managing digital platforms supporting medical, regulatory, and safety operations.
  3. Strong understanding of Medical Affairs, Regulatory Affairs, and Pharmacovigilance processes.
  4. Demonstrated leadership capabilities with experience in managing and developing high-performing teams.
  5. Excellent communication skills and the ability to engage effectively with diverse stakeholders.
  6. Solid experience in evaluating, negotiating, and managing contracts and Statements of Work with technology vendors and service partners.
  7. Comprehensive knowledge of quality and regulatory requirements, including industry standards such as 21 CFR Part 11.
  8. Strong problem-solving skills and a consistent record of successful project execution.
  9. Proven know-how with Veeva and ARIS global systems

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