
Clinical Lead MDR
16 hours ago
At TN Sweden, we are a leading global Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service capabilities, resourcing and Functional Service (FSP) solutions.
The Clinical Lead MDR is responsible for leading and coordinating efforts to ensure adherence to Medical Device Regulation (MDR) and related regulatory frameworks. This includes developing project plans, setting goals, managing resources, mitigating risks, and ensuring timely delivery within scope.
As part of our SRS/FSP team, you will be dedicated to one sponsor.
Key Responsibilities:- Oversee the planning, execution, and completion of projects related to MDR compliance
- Develop and implement strategies to align with regulatory requirements
- Coordinate with cross-functional teams, including legal, quality assurance, and operations
- Ensure project milestones are met while maintaining high-quality standards
- Manage risk assessment and mitigation strategies
- Communicate project updates to stakeholders and regulatory bodies
Qualifications:
- Minimum three years of experience in project management
- Strong knowledge of MDR and regulatory compliance frameworks
- Experience in implementing regulatory policies and management systems
- Proven ability to lead teams and engage stakeholders
- Strong communication and problem-solving skills
- Fluency in both Swedish and English
We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment. You'll be joining a team that values collaboration, innovation, and making a difference in the lives of patients.
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