Clinical Compliance Lead

3 days ago


Stockholm, Stockholm, Sweden TN Sweden Full time

TN Sweden is a leading Contract Research Organization (CRO) partnering with biotechnology and pharmaceutical companies throughout their entire clinical development journey.

We are seeking an experienced Clinical Compliance Lead to lead and coordinate efforts to ensure adherence to Medical Device Regulation (MDR) and related regulatory frameworks.

Key Responsibilities:
  • Develop and implement project plans to align with regulatory requirements
  • Oversee the planning, execution, and completion of projects related to MDR compliance
  • Cultivate strong relationships with cross-functional teams, including legal, quality assurance, and operations
  • Ensure timely delivery of high-quality results while managing risk assessment and mitigation strategies
  • Communicate project updates to stakeholders and regulatory bodies
Requirements:
  • Minimum three years of experience in project management with a focus on regulatory compliance
  • Proven expertise in MDR and regulatory frameworks
  • Strong knowledge of implementing regulatory policies and management systems
  • Excellent communication and problem-solving skills
  • Fluency in both Swedish and English
About Us:

We offer a competitive compensation package, comprehensive benefits, and opportunities for personal and professional growth in a collaborative environment that values innovation and making a difference in patient lives.



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