Clinical Trial Management System Specialist

hace 4 semanas

Barcelona, Barcelona, España Veeva Systems A tiempo completo

Position Overview

Are you proficient in the implementation or upkeep of a Clinical Trial Management System? Do you have a passion for addressing clinical trial challenges through innovative CTMS solutions? Are you knowledgeable about monitoring visits, recruitment strategies, or site payment processes?

As a key member of our Professional Services team, your role will involve comprehending our clients' challenges and clinical requirements, translating those needs into effective solution designs within our Clinical Vault, providing training, and assisting clients during application validation.

If you are a Senior Consultant, you will also take on the responsibility of guiding and mentoring skilled project team members in the implementation and configuration of the tailored solutions you design.

This position offers the flexibility to work remotely from any location within Europe, or from one of our offices if preferred.

Key Responsibilities

  • Engage in workshops to explore Clinical Trial Management System requirements with clients.
  • Advise clients on optimal design choices.
  • Document design choices and configure Veeva Vault or provide guidance on its configuration to align with client needs.
  • Assist clients during validation processes.
  • Deliver training sessions, either onsite or remotely.
  • Collaborate with our product team on enhancement requests informed by project insights.
  • Enjoy working with a talented and dynamic team.

Qualifications

  • Experience in implementing or maintaining a CTMS solution from a vendor, business, or IT perspective.
  • Familiarity with systems such as IMPACT CTMS, Medidata Rave, Bioclinica CTMS, or other smaller CTMS providers.
  • Demonstrated ability to work autonomously in a fast-paced environment.
  • Willingness to travel as necessary.
  • Bachelor's degree or higher.
  • Strong communication skills in English.
  • Eligible candidates must have legal authorization to work within the European Union.

Preferred Qualifications

  • Degree in life sciences or computer science.
  • Experience in clinical trial management.
  • Understanding of technical concepts such as web services or SQL queries.
  • Knowledge of Software Validation in the life sciences sector.
  • Experience with SaaS/Cloud solutions.
  • Familiarity with Agile project methodologies.
  • Experience in demonstrating software applications during pre-sales activities.
  • Fluency in additional languages such as German, French, Italian, or Spanish is a plus.

Benefits

  • Competitive compensation package.
  • Opportunities for continuous learning and professional development.
  • Health and wellness initiatives.

Veeva Systems is committed to fostering a culture of inclusion and building a diverse workforce. We value individuals for their unique contributions and experiences.

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