Clinical Trial Manager, FSP - Lead High-Impact Trials

MAV Healthcare; Santiago; Vor Ort; CLP 48.000.000 - 62.000.000; Vollzeit

Zusammenfassung

Santiago ThermoFisher Scientific is seeking a Sr CTM to oversee clinical trials from setup to delivery. You will lead the clinical team, ensure data quality, and maintain adherence to contract terms and regulatory standards.

The role involves coordinating with sites, vendors, and internal groups to meet project milestones. Ideal candidates will have a strong background in clinical monitoring, budgeting, and regulatory submissions, with proven leadership in multi-site studies and global teams.

Qualifikationen

• Leadership and mentoring experience within cross-functional teams.
• Strong planning and organizational abilities for prioritizing workload.
• Solid communication and problem-solving in a multicultural matrix environment.

Aufgaben

• Manage all clinical operations and quality aspects of allocated studies in compliance with ICH GCP.
• Develop clinical tools and assist in Master Action Plan and Trial Master File readiness.
• Lead team meetings, coordinate start-up activities, and ensure timely regulatory submissions where appropriate.
• Monitor timelines and budgets, provide status updates, and manage CRF collection and query resolution.
• Collaborate with sites and internal departments to meet project deliverables and client expectations.

Kenntnisse

Leadership

Planning

Interpersonal skills

Communication

Budgeting

Attention to detail

Clinical monitoring knowledge

Ausbildung

Bachelor's degree or equivalent

Tools

Outlook

Excel

Word

Jobbeschreibung

Santiago ThermoFisher Scientific is seeking a Sr CTM to oversee clinical trials from setup to delivery. You will lead the clinical team, ensure data quality, and maintain adherence to contract terms and regulatory standards.

The role involves coordinating with sites, vendors, and internal groups to meet project milestones. Ideal candidates will have a strong background in clinical monitoring, budgeting, and regulatory submissions, with proven leadership in multi-site studies and global teams.