Remote Clinical Trial Manager for Global Studies

Placements24; Cape Town; Hybrid; ZAR 900,000 - 1,300,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

Remote work

Professional development

Flexible schedule

Job summary

Placements24 is seeking an experienced Remote Clinical Trial Manager to oversee multiple clinical studies from initiation to close-out. This fully remote role is based in South Africa, offering flexibility to work from anywhere within the country.

You will plan, execute, and monitor trials, ensuring GCP/ICH compliance and efficient collaboration with investigators, sites, and CROs. Strong communication and organizational skills are essential to drive successful outcomes.

Qualifications

• Bachelor’s degree in life sciences, nursing, or related field.
• Advanced degree preferred.
• Minimum 7 years in clinical research with at least 3 years as Clinical Trial Manager.
• Proven experience in multi-center, international trials.
• Strong knowledge of GCP, ICH guidelines, and regulatory submissions.
• Proficiency with CTMS and EDC systems.

Responsibilities

• Develop and manage trial protocols, budgets, and timelines.
• Oversee investigator/site selection and management, ensuring study requirements.
• Monitor trial progress, identify risks, and implement corrective actions.
• Ensure compliance with GCP, ICH guidelines, and regulatory standards.
• Manage CROs and third-party vendors involved in trials.
• Present regular progress reports to senior management.

Skills

Project management

GCP/ICH knowledge

Multi-center coordination

Stakeholder communication

Vendor management

Education

Bachelor's degree in life sciences or related field

Advanced degree preferred

Tools

CTMS

EDC systems

Job description

Placements24 is seeking an experienced Remote Clinical Trial Manager to oversee multiple clinical studies from initiation to close-out. This fully remote role is based in South Africa, offering flexibility to work from anywhere within the country.

You will plan, execute, and monitor trials, ensuring GCP/ICH compliance and efficient collaboration with investigators, sites, and CROs. Strong communication and organizational skills are essential to drive successful outcomes.