Site Activation Specialist II – Min 2 years of regulatory experience in Mexico

This is a fully remote position, open to applicants in Mexico.

📋 Description

• Accountable for ensuring high-quality deliverables at the national level.

• Operates within the established submission and approval timelines while monitoring milestone progress.

• Oversees fundamental financial components of the project.

• Reviews and adheres to Standard Operating Procedures (SOPs) and Work Instructions (WI).

• Aids in the ongoing enhancement of quality across all Site Start-Up (SSU) elements at the national level.

• Serves as a Subject Matter Expert for in-country performance within Site Start-Up activities.

⛳️ Requirements

• Minimum of 2 years of regulatory experience in Mexico.

• Bachelor’s Degree.

• Comprehensive knowledge of the clinical trial process across Phases II-IV and ICH GCP.

• Proficient in understanding clinical protocols and related study specifications.

• Excellent organizational skills with the capacity to manage multiple tasks effectively.

• Quality-focused in all activities undertaken.

🏝️ Benefits

• We are dedicated to nurturing our employees through career development and advancement opportunities.

• Supportive and engaged management team.

• Technical and therapeutic training provided.

• Peer recognition along with a comprehensive rewards program.

• Commitment to fostering an inclusive workplace culture.