Site Activation Manager - Europe - Remote

Worldwide Clinical Trials

4 years cro experience in study start-up
Oncology therapeutic area expertise
Ich gcp and fda/eu regulatory knowledge
The company is a global midsize CRO with over 3,500 experts dedicated to pioneering approaches for curing persistent diseases

Job Summary

  • The company is a global midsize CRO with over 3,500 experts dedicated to pioneering approaches for curing persistent diseases.
  • This role serves as the primary accountability for site activation activities within the Oncology therapeutic area, ensuring milestones are met on time and within budget.
  • Candidates must demonstrate strong leadership skills and a deep understanding of ICH GCP guidelines along with FDA and EU clinical trial regulations.

Matching Summary

The company is a global midsize CRO with over 3,500 experts dedicated to pioneering approaches for curing persistent diseases.

Skills & Requirements

Must-have

  • 4 years CRO experience in Study Start-Up
  • Oncology therapeutic area expertise
  • ICH GCP and FDA/EU regulatory knowledge
  • Site identification and contract management
  • Budget tracking and change control

Nice-to-have

  • Cross-cultural communication skills
  • Business development proposal support
  • SOP development and continuous improvement
  • Risk assessment and mitigation planning
  • Digital systems aptitude

Key Requirements

  • Minimum four-year degree or nursing degree
  • Minimum 4 years CRO experience in Study Start-Up
  • Country lead or manager experience required

Work Rights

Not specified

Tailored Resume

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