Principal Investigator (Medtech)

TL;DR

Principal Investigator (Medtech): Conducting and supervising decentralized clinical research trials for infant formula growth monitoring studies with an accent on regulatory compliance, participant safety, and data integrity. Focus on performing telehealth-based subject consent, reviewing inclusion/exclusion criteria, and providing medical oversight for decentralized clinical activities.

Location: Must be based in the United Kingdom

Company

A research organization helping biotech, medtech, and specialty pharma companies transform breakthrough science into new medicines, devices, and diagnostics.

What you will do

• Conduct and supervise research activities for infant formula growth monitoring studies in accordance with local and international regulations.
• Perform subject consent and review inclusion/exclusion criteria via telehealth video conferencing.
• Obtain ethics approval prior to participant enrollment and ensure ongoing compliance.
• Review study data and records to maintain participant safety and data integrity.
• Provide medical expertise and input into protocol design and clinical development plans.
• Maintain medical and regulatory accountability for study conduct and oversight of delegated personnel.

Requirements

• Medical degree with an active, unrestricted medical license.
• Must be based in the United Kingdom.
• 3-5 years of experience as a Principal Investigator.
• Experience with telehealth, growth curves, and WHO growth charts for children under 2 years old.
• Familiarity with infant milestones and infant formula.
• Preferably a Pediatrician.

Culture & Benefits

• Flexible work environment focused on work-life balance.
• Opportunity to contribute to life-changing medical innovations.
• Supportive team culture where individual ideas and contributions are valued.
• Part-time role with anticipated weekly hours ramping up to 4-6 by February 2027.