Medical Affairs Manager

2 weeks ago


Stockholm, Stockholm, Sweden TN Sweden Full time

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Our client is a dynamic medical device business at the forefront of biotechnological manufacturing methods and the promotion of cutting-edge biomaterials. Fueled with a commitment to innovate, they utilise their expertise to spearhead new biotechnologies. With robust R&D resources, the company is gearing up for expansion and is set to revolutionise various fields such as aesthetics, orthopaedics, and plastic surgery. Due to their continued growth, they are now looking for a Medical Affairs Manager to join their Stockholm office.

As a Medical Affairs Manager you will be responsible for providing medical and scientific support for the company's medical device products. You will collaborate with the company's management, regulatory affairs, and commercial teams to guarantee the safety and effectiveness of the company's products. Additionally, you'll act as the go-to authority and liaison for external stakeholders, such as KOLs and HCPs.

Key responsibilities:

  • Plan and oversee scientific and clinical studies to meet regulatory and marketing needs, including assisting in the creation of clinical study protocols and analyzing study data.
  • Work closely with the regulatory affairs team to compile regulatory submissions and aid in securing product approvals.
  • Engage in the formulation and execution of medical affairs strategies and plans to support the marketing and sales efforts.
  • Assess and appraise scientific literature pertinent to the company's products and market.
  • Develop and provide scientific training materials to both internal and external stakeholders.

To be considered for the role, you must closely match the following criteria:

  • Possession of an MD, PhD, PharmD, or a similar advanced degree in a relevant scientific field.
  • Previous experience in medical affairs, scientific communications, or clinical research in the pharmaceutical or medical device sector.
  • A solid grasp of drug and medical device development and regulatory procedures.
  • Exceptional written and spoken communication skills in English are essential. Proficiency in Swedish for business purposes is highly advantageous.
  • The ability to interpret and present scientific data to a diverse range of audiences.
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