Lead Global Clinical Trial Manager – CVRM

KCR Placement; Buenos Aires; Vor Ort; ARS 1.800.000 - 3.200.000; Vollzeit

Benefits dieser Stelle

Annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme (

Life assurance

Flexible country-specific benefits

Zusammenfassung

ICON Strategic Solutions seeks a Clinical Trial Manager to oversee day-to-day trial operations across global programmes. You will guide your team, coordinate cross-functional efforts, and ensure adherence to timelines, budget, and quality standards while maintaining regulatory and ethical compliance.

You will collaborate with investigators and stakeholders, manage vendor relationships, and address risk and design considerations to deliver high-quality outcomes for patients worldwide.

Qualifikationen

• University degree in medicine, science, or equivalent, with proven global trial experience.
• Experience managing global clinical study projects.
• Strong track record leading local, regional, and international vendors.
• Previous experience as a Senior CRA.
• Advanced English proficiency.

Aufgaben

• Plan and manage all aspects of clinical trials, ensuring timelines, budget, and quality.
• Collaborate with cross-functional teams to establish trial protocols and procedures.
• Build and manage relationships with trial investigators and stakeholders.
• Ensure trials comply with local, national, and international regulations and ethical guidelines.
• Problem-solve and make critical decisions on trial design, vendor selection, and risk management.

Kenntnisse

Clinical trial management

Vendor management

Team leadership

Regulatory compliance

English proficiency

Ausbildung

University degree in medicine, science, or equivalent

Jobbeschreibung

ICON Strategic Solutions seeks a Clinical Trial Manager to oversee day-to-day trial operations across global programmes. You will guide your team, coordinate cross-functional efforts, and ensure adherence to timelines, budget, and quality standards while maintaining regulatory and ethical compliance.

You will collaborate with investigators and stakeholders, manage vendor relationships, and address risk and design considerations to deliver high-quality outcomes for patients worldwide.