About VitalMetrics

VitalMetrics is a Swedish performance-focused wellness technology platform combining biomarker insights, training data and lifestyle analytics into a unified digital Health OS.

We operate within a wellness and performance framework and collaborate with certified laboratory partners for biomarker analysis.

The Role

We are seeking a licensed physician in Sweden for an external regulatory collaboration.

This is not a clinical employment role. The collaboration is designed to support laboratory-related regulatory requirements connected to biomarker testing performed by accredited laboratory partners.

The role involves:

• Acting as external medical signatory where required

• Reviewing specific laboratory cases when necessary

• Ensuring regulatory compliance within Swedish frameworks

• Being available for limited case-based consultation

The physician will act as responsible remitting doctor for predefined, recurring biomarker test panels within a structured operational framework.

The role includes medical sign-off of standardized test packages and individual medical assessment in cases of laboratory-reported deviations.

The collaboration does not involve ongoing patient treatment or continuous clinical workload beyond the defined laboratory-related scope.

Scope & Commitment

• Remote

• Very low time commitment (estimated 5–30 minutes per month depending on volume)

• Contract-based collaboration

• Flexible structure

Compensation

• Fixed monthly compensation

• Additional compensation per reviewed case

The structure is designed to reflect minimal time commitment while ensuring professional accountability.

Details are discussed individually.

Requirements

• Licensed physician in Sweden

• Valid Swedish medical license (Legitimerad läkare)

• Understanding of regulatory and laboratory frameworks

• Professional independence

• Ability to invoice through own company (F-tax registered) or via freelance invoicing service

Ideal Profile

This role may suit a physician who:

• Prefers clearly defined, low-volume regulatory responsibilities

• Has experience with laboratory-related processes

• Values remote, structured collaboration with minimal time commitment

• Is interested in a predictable supplemental professional income alongside primary clinical or non-clinical work