Remote Regulatory & Start-Up Specialist (Spain)

Precision for Medicine; United States; Remote; USD 104,000 - 150,000; Full time

Benefits offered by this job

Equal Opportunity Employer

Professional growth

Job summary

Precision for Medicine, a global CRO, seeks a remote regulatory Start-Up expert based in Spain to drive site activation, manage regulatory submissions, and lead contract negotiations with global teams. This role engages with clinical operations, project management, and other functions to ensure regulatory excellence.

The candidate will coordinate with ethics committees and authorities, maintain regulatory intelligence tools, and support audits and inspections.

Qualifications

• Bachelor's degree in life sciences or RN; regulatory/start-up experience in CRO/pharma preferred.
• Fluent in English and Portuguese.
• Strong communication and organizational skills; proficiency with regulatory tools.

Responsibilities

• Prepare and submit Clinical Trial Applications to authorities and ethics committees.
• Act as SME for site activation, including critical path data, budgets and contracts.
• Provide updates to Start Up leads, maintain regulatory intelligence tools, and support audits/inspections.

Skills

Regulatory submissions

Contract negotiations

English and Portuguese fluency

Communication

Education

Bachelor's degree in life sciences or RN

Tools

Regulatory databases

Computerized systems

Job description

Precision for Medicine, a global CRO, seeks a remote regulatory Start-Up expert based in Spain to drive site activation, manage regulatory submissions, and lead contract negotiations with global teams. This role engages with clinical operations, project management, and other functions to ensure regulatory excellence.

The candidate will coordinate with ethics committees and authorities, maintain regulatory intelligence tools, and support audits and inspections.