
Scientific Liaison Manager
4 days ago
As a Medical Affairs Manager at TN Sweden, you will play a crucial role in supporting the company's growth and innovation in the medical device industry.
Your primary responsibility will be to provide medical and scientific support for the company's products, ensuring that they meet regulatory requirements and effectively communicate their value to customers and stakeholders.
To achieve this, you will work closely with the management, regulatory affairs, and commercial teams to develop and implement medical affairs strategies that align with the company's overall goals.
You will also be responsible for planning and overseeing scientific and clinical studies, working closely with the regulatory affairs team to compile regulatory submissions, and evaluating and assessing relevant scientific literature.
In addition to these key responsibilities, you will create and provide scientific training materials to both internal and external stakeholders.
Key Responsibilities:- Plan and oversee scientific and clinical studies to meet regulatory and marketing needs.
- Work closely with the regulatory affairs team to compile regulatory submissions.
- Develop and execute medical affairs strategies and plans.
- Evaluate and assess relevant scientific literature.
- Create and provide scientific training materials.
- Possession of an MD, PhD, PharmD, or similar advanced degree in a relevant scientific field.
- Previous experience in medical affairs, scientific communications, or clinical research.
- Strong understanding of drug and medical device development and regulatory procedures.
- Exceptional written and spoken communication skills in English.
- Able to interpret and present scientific data to diverse audiences.
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