Ctis (clinical Trial Information System) - Team Specialist

Roche UK

Riga, Latvia
2,400 eur grosspmnthly; not specified; not specifi...
Hybrid
Manage eu cta submission portal
Coordinate cta compilation and submission
Monitor and handle regulator information
As a CTIS-team Specialist, you will manage the administration of the EU CTA submission portal, coordinate and support the compilation, completion and submission of EU Clinical Trial Applications (CTAs)

Job Summary

  • As a CTIS-team Specialist, you will manage the administration of the EU CTA submission portal, coordinate and support the compilation, completion and submission of EU Clinical Trial Applications (CTAs).
  • Roche provides constant development opportunities, free language courses & training, the possibility of international assignments, and internal position changes.
  • Work in a hybrid model (2 days/week from the office) within a global diverse community where we learn from each other.

Matching Summary

As a CTIS-team Specialist, you will manage the administration of the EU CTA submission portal, coordinate and support the compilation, completion and submission of EU Clinical Trial Applications (CTAs).

Salary

2400 EUR gross/monthly; Not specified; Not specified

Skills & Requirements

Must-have

  • Manage EU CTA submission portal
  • Coordinate CTA compilation and submission
  • Monitor and handle regulator information
  • Track and archive HA inquiries
  • Proficiency in IT skills
  • Data and document management skills

Nice-to-have

  • Embraced for unique qualities
  • Open dialogue and genuine connections
  • Additional languages a plus
  • Assess automation opportunities
  • Shape your own career

Key Requirements

  • Minimum BA or BS degree in relevant field
  • Experience in similar role
  • Strong communication skills in English

Work Rights

Not specified

Tailored Resume

Cover Letter