Senior Pharma Clinical Research Associate - Impactful Trials

Placements24; Soweto; Hybrid; ZAR 600,000 - 800,000; Full time

Benefits offered by this job

Competitive salary

Travel allowances

Health insurance

Professional development

Collaborative work environment

Job summary

Placements24 is seeking a Senior Pharmaceutical Clinical Research Associate to support trials in Soweto, Gauteng. The role focuses on site selection, initiation, monitoring, and close-out visits, ensuring data integrity and participant safety.

You will monitor adherence to protocols and regulatory requirements, train site staff, manage trial supplies, and collaborate with cross-functional teams to drive quality and regulatory compliance across multiple sites in the Soweto area.

Qualifications

• Bachelor's degree in life science, nursing, pharmacy or related field.
• 4–6 years as a Clinical Research Associate with ICH-GCP knowledge.
• Experience monitoring Phase II/III clinical trials and site management.

Responsibilities

• Conduct site selection, initiation, monitoring and close-out visits per GCP and protocol.
• Ensure data quality and integrity across study sites.
• Verify adherence to protocol, plan and regulatory requirements.
• Maintain relationships with investigative sites and staff.
• Train and mentor site personnel on study procedures and regulatory requirements.
• Identify and address site risks and issues.
• Prepare monitoring visit reports and track action items.
• Manage investigational product accountability and supplies.
• Collaborate with project managers, data managers and study physicians.
• Stay updated on clinical research best practices and regulatory updates.

Skills

Site monitoring

GCP/ICH knowledge

CTMS experience

EDC experience

Travel readiness

Education

Bachelor's degree in life sciences

Tools

CTMS

EDC systems

Job description

Placements24 is seeking a Senior Pharmaceutical Clinical Research Associate to support trials in Soweto, Gauteng. The role focuses on site selection, initiation, monitoring, and close-out visits, ensuring data integrity and participant safety.

You will monitor adherence to protocols and regulatory requirements, train site staff, manage trial supplies, and collaborate with cross-functional teams to drive quality and regulatory compliance across multiple sites in the Soweto area.