Overview

As a Senior Clinical Trial Manager, you will oversee site management, monitoring, and data integrity for oncology trials from a home base in Spain. You'll coordinate a cross-functional clinical team to achieve study milestones, manage risks, and ensure protocol and regulatory compliance. You'll act as a key liaison with investigators, sites, and sponsors, driving quality and delivery while supporting inspections readiness.

This role offers impact across the drug development continuum, with opportunities to shape trial delivery and processes in a fast-paced, inclusive environment.

Compensaciones / Beneficios career development inclusive culture total rewards program technical and therapeutic area training

Responsabilidades

Oversee site management, clinical/central monitoring deliverables with emphasis on patient safety and data integrity

Manage site interactions from activation to closeout, including recruitment and investigator payments

Identify and mitigate risks using data, escalating issues to project management as needed

Coordinate and review study scope, budget, and protocol content to align with contractual obligations

Lead and participate in key meetings (e.g., Kick Off) and provide status updates on deliverables and risks

Develop and maintain study tools/templates (e.g., Clinical Monitoring Plan) and ensure CTMS and dashboards are usable

Provide initial and ongoing training to study teams on protocols, CRFs, SOPs, data plans,



and timelines

Oversee resourcing allocations for CRAs and Central Monitors and monitor team conduct and delivery quality

Review monitoring documentation and ensure timely updates in CTMS and other systems

Interact with client and other functions to resolve obstacles and ensure compliance with protocol and regulatory requirements

Support inspections readiness and implement corrective action plans as needed

Mentor and coach CTMs on clinical delivery, risk assessment, and action implementation

May coordinate activities across a portfolio of projects or larger, more complex trials

Requisitos principales Bachelor's degree or RN in a related field or equivalent

Proven vendor management experience

Integral study management experience

Experience in Oncology clinical trials

Strong experience reviewing and overseeing study plans and documentation

Ability to lead and align teams to milestones

Experience in international environments

Expertise in site management and monitoring (clinical or central)

Knowledge of risk-based monitoring (preferred)

Budget management and understanding of clinical trial financial principles

Knowledge of GCP/ICH and regulatory requirements

Strong computer and data skills; conflict resolution and problem-solving abilities

Willingness to travel ~20%

leadership communication problem solving

CTMS

EDC eDiary

📌 Global Sr CTM - Home Based in SPAIN. FSP. Oncology experience is required.. (León)
🏢 Syneos Health
📍 León