Senior Clinical Trial Manager — Remote, Global

Placements24; Klerksdorp; A distancia; ZAR 900.000 - 1.500.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Health insurance

Retirement planning

Life assurance

Employee assistance program

Descripción de la vacante

ICON Strategic Solutions is seeking a Senior Clinical Trial Manager based in Johannesburg to lead day-to-day management of clinical trials within a sponsor-dedicated model. You will oversee study delivery, timelines, budgets, and quality across programmes.

You will partner with cross-functional teams, investigators, and stakeholders to implement protocols, manage risks, and ensure regulatory and ethical compliance. Travel about 25% is required; a medical or science degree is essential.

Formación

• University degree in medicine, science, or equivalent combination of education & experience.
• Demonstrated ability to drive the clinical deliverables of a study.
• Subject matter expertise in the designated therapeutic area.
• Prior monitoring experience is preferred.
• Willingness to travel as required (approximately 25%).

Responsabilidades

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

Conocimientos

Clinical trial management

Project leadership

Regulatory compliance

Travel readiness

Educación

University degree in medicine or science

Descripción del empleo

ICON Strategic Solutions is seeking a Senior Clinical Trial Manager based in Johannesburg to lead day-to-day management of clinical trials within a sponsor-dedicated model. You will oversee study delivery, timelines, budgets, and quality across programmes.

You will partner with cross-functional teams, investigators, and stakeholders to implement protocols, manage risks, and ensure regulatory and ethical compliance. Travel about 25% is required; a medical or science degree is essential.