Principal Investigator

41 Premier Research Group Limited

England

On-site

GBP 90,000 - 120,000

Full time

14 days+

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Job summary

Premier Research is seeking a Principal Investigator to join our Virtual Research Group focused on infant formula growth monitoring studies in England.

You will conduct and supervise decentralized clinical research trials, obtain ethics approvals, review data and ensure participant safety, while providing medical expertise and regulatory input to protocol development.

Qualifications

  • Must hold a medical degree with an active, unrestricted license.
  • Pediatric experience preferred and knowledge of infant milestones.
  • Experience with decentralized or remote trial conduct.
  • Familiar with WHO growth charts and growth percentiles.

Responsibilities

  • Lead and supervise decentralized clinical trials ensuring patient safety and data integrity.
  • Obtain ethics approvals and regulatory documentation.
  • Provide medical input into protocol design and development plans.
  • Present at meetings as needed.
  • Maintain medical and regulatory accountability for study conduct.

Skills

Clinical research
Telehealth experience
Regulatory compliance
Data monitoring

Education

Medical degree with active license
Pediatric specialization (preferred)

Tools

Telehealth platforms

Job description

Premier Research is looking for a Principal Investigator to join our Virtual Research Group team.

What You'll Be Doing:
  • As the Principal Investigator for decentralized clinical research trials you will personally conduct and supervise research activities for infant formula growth monitoring studies in England in accordance with applicable local, regional, and international regulations and ethics committee requirements while ensuring the rights, safety, and welfare of the participants are protected at all times.
  • Will be comfortable with a decentralized (also known as a direct‑to‑subject or site‑less) clinical research trial in which subject consent and review of inclusion/exclusion criteria will be performed through telehealth video conferencing.
  • Obtaining ethics approval prior to any participant enrollment.
  • Routinely performs data and study records review to ensure participant safety and data integrity.
  • Providing medical expertise and support.
  • Providing medical input into the protocol design and clinical development plans.
  • Contributing to the medical input and review of regulatory documents.
  • May present at Investigator, Customer, training, and/or bid defense meetings, as needed.
  • Maintaining ultimate medical and regulatory accountability for study conduct, including oversight of decentralized and remote activities performed by delegated personnel, vendors, and home healthcare providers.
What We Are Searching For:
  • Medical degree with an active, unrestricted medical license.
  • Preferably a Pediatrician.
  • Should be familiar with infant milestones and infant formula.
  • Should be experienced with telehealth, plotting growth curves, understanding percentiles and be familiar with WHO growth charts for under 2 year olds.
  • Should have 3-5 years of principal investigator experience.
  • The target to hire for this role is early September with anticipated weekly hours ramping up to between 4-6 by February 2027.
  • Ahead of then there will be a hold on activities / expected hours other than SIV and training between September to January, when consent begins.
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