Regulatory and Start Up Specialist (Portuguese speaker)

Key Responsibilities:

• Prepare and submit Clinical Trial Application forms and dossiers to Competent Authorities, Ethics Committees, and other local bodies, ensuring all necessary approvals.
• Act as a Subject Matter Expert for site activation, including critical path data, budgets, and contract negotiations.
• Provide regular updates to Start Up leads and project teams, maintain regulatory intelligence tools, and support audits and inspections.

Qualifications:

• Bachelor's degree in life sciences or related field, or RN, with experience in regulatory and start-up roles in CRO/pharma.
• Strong negotiation skills for contracts and budgets, and fluency in English and Portuguese.
• Excellent communication, organizational skills, and proficiency in computerized systems.

Work Details:

• This is a remote position based in Spain, collaborating with global teams.
• You will work closely with Clinical Operations, Project Management, and other key functions.

About the Team:

• Precision for Medicine is committed to advancing precision medicine and offers a dynamic, collaborative environment.
• They are an Equal Opportunity Employer and support professional growth.