This is a fully remote position, open to applicants in Mexico, +3 more countries.

📋 Description

• Identify and analyze issues and trends in operational and patient clinical trial data utilizing analytical or statistical methodologies.

• Utilize operational expertise and knowledge to assess issues and derive conclusions from analyzed data.

• Inform project team members about issues and potential risks for necessary follow-up actions.

• Perform risk assessments, develop monitoring plans, ensure sponsor oversight, conduct trend analysis, identify signals, strategize site monitoring, and maintain regulatory compliance and readiness for inspections.

• Collaborate within a Functional Service Partnership dedicated to a particular pharmaceutical client.

⛳️ Requirements

• A degree in Life Sciences or a related discipline, or equivalent professional experience as allowed by the approved job description.

• A minimum of 3 years of experience, as specified in the client's job description, subject to verification against the requirements for the Sr CM Analyst II role.

• In-depth understanding of Site Monitoring and Site Management.

• Excellent communication abilities.

• Proven leadership skills.

• Experience collaborating with cross-functional teams.

• Familiarity with risk assessments, monitoring plans, sponsor oversight, trend analysis, signal detection, site monitoring strategies, regulatory compliance, and inspection readiness activities.