UK Regulatory & Start-Up Specialist

Precision Medicine Group; United Kingdom; Remote; GBP 40.000 - 68.000; Vollzeit

Benefits dieser Stelle

Equal opportunity employer

Reasonable accommodation

Zusammenfassung

Precision for Medicine is seeking a Regulatory and Start Up Specialist in the UK to join our growing regulatory team. You will drive site activation readiness, prepare regulatory submissions, and support contract and budget negotiations within the UK.

The ideal candidate has a life sciences degree, English fluency, and at least two years of relevant regulatory/start-up experience in CRO/pharmaceutical settings. Collaboration with cross-functional teams is essential to ensure timely approvals.

Qualifikationen

• Bachelor’s degree in life sciences or RN/healthcare background.
• Pharmacist qualification would be beneficial.
• At least 2 years of relevant regulatory/start-up experience.
• Fluency in English.

Aufgaben

• Deliver timely site activation readiness in the assigned country/sites.
• Prepare and submit Clinical Trial Applications and documentation to authorities.
• Provide regular updates to Start Up Lead/Regulatory Lead and Project Manager.
• Maintain project plans, trackers and regulatory intelligence tools.
• Coordinate translations and essential documents for site activation.

Kenntnisse

Communication

Organizational skills

English fluency

Ausbildung

Bachelor's degree in life sciences

RN qualification

Pharmacist background

Jobbeschreibung

Precision for Medicine is seeking a Regulatory and Start Up Specialist in the UK to join our growing regulatory team. You will drive site activation readiness, prepare regulatory submissions, and support contract and budget negotiations within the UK.

The ideal candidate has a life sciences degree, English fluency, and at least two years of relevant regulatory/start-up experience in CRO/pharmaceutical settings. Collaboration with cross-functional teams is essential to ensure timely approvals.