Study Start-up Lead

Roche

Leading study start-up strategy execution
Managing regulatory submissions to ha/ec
Overseeing icf management and compliance
The primary focus of this role is to drive efficient study start-up processes to contribute to the delivery of clinical trials to patients

Job Summary

  • The primary focus of this role is to drive efficient study start-up processes to contribute to the delivery of clinical trials to patients.
  • You will lead teams in creating start-up strategies that encompass proactive risk mitigation, regulatory compliance, and stakeholder liaison.
  • Roche offers a culture that encourages personal expression, open dialogue, and genuine connections where every voice matters.

Matching Summary

The primary focus of this role is to drive efficient study start-up processes to contribute to the delivery of clinical trials to patients.

Skills & Requirements

Must-have

  • Leading study start-up strategy execution
  • Managing regulatory submissions to HA/EC
  • Overseeing ICF management and compliance
  • Negotiating clinical site budgets and contracts
  • Proficiency in Veeva Vault and CTIS systems

Nice-to-have

  • Experience with process automation and innovation
  • Strong cross-functional collaboration skills
  • Ability to lead through complexity and ambiguity
  • Participation in external industry collaborations

Key Requirements

  • Degree in life sciences or equivalent
  • Postgraduate degree highly desirable
  • Demonstrated experience in clinical trial start-up
  • Fluency in English and host country language

Work Rights

Not specified

Tailored Resume

Cover Letter