Sr. Clinical Trial Specialist, Poland

175

Warsaw, Poland
Base: 173,000.00 zł - 284,000.00 zł; bonus: discre...
Bachelor's degree in life sciences
5 years clinical research experience
Sponsor or cro experience required
The role involves planning, executing, and managing clinical study projects to help change how the world prevents and detects cancer

Job Summary

  • The role involves planning, executing, and managing clinical study projects to help change how the world prevents and detects cancer.
  • Candidates must ensure operational and regulatory integrity of assigned studies while supporting FDA or other regulatory authority inspections.
  • The position offers a purpose-driven career with an inclusive culture and robust benefits to support employees working to help others.

Matching Summary

The role involves planning, executing, and managing clinical study projects to help change how the world prevents and detects cancer.

Salary

Base: 173,000.00 zł - 284,000.00 zł; Bonus: Discretionary bonus eligible; Benefits: Robust benefits package included

Skills & Requirements

Must-have

  • Bachelor's degree in life sciences
  • 5 years clinical research experience
  • Sponsor or CRO experience required
  • Good Clinical Practices knowledge
  • FDA submission process expertise
  • English fluency C1 or above

Nice-to-have

  • International study experience
  • IVDR and GDPR implementation
  • European language proficiency
  • Vendor oversight experience
  • Fast-paced environment adaptability
  • Strong problem-solving skills

Key Requirements

  • Minimum 5 years clinical research experience
  • At least one year sponsor/CRO experience
  • Authorization to work in Poland
  • No visa sponsorship available
  • Fluency in English (C1+)

Work Rights

Must be currently authorized to work in Poland

Tailored Resume

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