Clinical Trial Manager – Sponsor Dedicated

About the role

The Clinical Trial Manager – Sponsor Dedicated will oversee local clinical trial operations from start‑up through close‑out, ensuring compliance with sponsor SOPs, GCP and local regulations.

Key responsibilities

• Prepare high‑level budget estimates and detailed proposals, manage contracts with external service providers and monitor financial performance.
• Act as the primary contact for the trial at country level, track project timelines, patient recruitment rates and implement contingency plans.
• Maintain trial management systems, generate progress reports, and support health authority inspections and internal audits.
• Develop and review country‑specific informed consent documents and contribute to site recruitment strategies.

Required profile

• Bachelor’s degree in a health or science‑related field.
• Minimum 2 years of local/regional trial management experience in pharma or CRO, including work as a Clinical Research Associate.
• Strong knowledge of ICH‑GCP, sponsor SOPs, local regulations and therapeutic area specifics.
• Excellent decision‑making, financial management and communication skills in English and Spanish.

Required skills

• ICH‑GCP compliance
• Clinical trial management systems
• Budgeting and contract management
• Proficiency with standard office and trial‑related software