UK Regulatory & Start-Up Specialist (Remote)

Precision Medicine Group, LLC.; United Kingdom; Remote; GBP 45,000 - 65,000; Full time

Job summary

Precision for Medicine, part of Precision Medicine Group, is seeking a Regulatory and Start Up Specialist based in the UK. The role focuses on regulatory submissions, site activation, and contract/budget negotiations within CRO/pharma environments.

We value strong communication and organizational skills, English fluency, and 2+ years of related experience. This remote UK position requires knowledge of local regulations and cross-functional collaboration with Clinical Operations and Regulatory

Qualifications

• Bachelor’s degree in life sciences or RN; pharma/healthcare experience preferred.
• 2+ years of regulatory/start-up experience in CRO or pharma.
• Strong communication and organizational skills.
• Fluent in English.
• Experience with regulatory submissions and site contracts is a plus.

Responsibilities

• Prepare Clinical Trial Application forms and submission dossiers for authorities and ethics committees.
• Interact with CA/EC for study purposes and respond to inquiries.
• Provide updates on submissions to study leadership and project teams.
• Maintain project plans, trackers, and regulatory intelligence tools.
• Support start-up plans, IMP release requirements, and essential document review.

Skills

Regulatory submissions experience

Budget negotiations

Communication skills

Organizational skills

English fluency

Education

Bachelor’s degree in life sciences or RN

Advanced degree in medical or life sciences (MD/PhD/PharmD) / RAC

Job description

Precision for Medicine, part of Precision Medicine Group, is seeking a Regulatory and Start Up Specialist based in the UK. The role focuses on regulatory submissions, site activation, and contract/budget negotiations within CRO/pharma environments.

We value strong communication and organizational skills, English fluency, and 2+ years of related experience. This remote UK position requires knowledge of local regulations and cross-functional collaboration with Clinical Operations and Regulatory