Medical Affairs Manager

Guided Solutions; Sweden; On-site; SEK 600 000 - 900 000; Full time

Job summary

A leading medical device company in Sweden seeks a Medical Affairs Manager for their Stockholm office. This role involves providing critical medical and scientific support for products, collaborating across teams to ensure compliance and safety. Candidates must possess an advanced scientific degree and relevant experience in the medical device or pharmaceutical industry.

Qualifications

• Advanced degree in a relevant scientific field is required.
• Experience in medical affairs or clinical research is essential.
• Exceptional written and spoken English; proficiency in Swedish is a plus.

Responsibilities

• Provide medical and scientific support for medical device products.
• Plan and oversee scientific and clinical studies.
• Collaborate with regulatory affairs to secure product approvals.

Skills

Scientific communication

Data interpretation

Medical knowledge

Education

MD, PhD, PharmD or similar degree

Job description

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Our client is a Sweden-headquartered medical device business that focuses on biotechnological manufacturing methods and the promotion of cutting-edge and forward-looking biomaterials. Powered by a commitment to change and advancement, they harness their exceptional expertise and distinct capabilities to pioneer new biotechnologies. Due to their continued growth, they are now looking for aMedical Affairs Managerto 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.