Hybrid Cardio CRA - Trial Monitoring & Compliance

Placements24; Birmingham; Hybrid; GBP 32,000 - 45,000; Full time

Benefits offered by this job

Competitive remuneration package

Professional development

Hybrid work model

Collaborative team

Job summary

Placements24 seeks a diligent Clinical Research Associate (CRA) to join a cardiovascular trials team in Gauteng. The role centers on monitoring trials to ensure data integrity, patient safety, and regulatory compliance, with a hybrid work model balancing remote monitoring and essential site visits.

The successful candidate will conduct site visits, perform SDV, train site staff, manage trial documents, and collaborate with data management and regulatory teams to support study delivery.

Qualifications

• Bachelor's degree in a life science, nursing, or related field.
• Master's degree or equivalent experience is a plus.
• Minimum of 3 years of experience as a Clinical Research Associate.
• Solid knowledge of ICH-GCP guidelines and regulatory requirements.
• Experience monitoring cardiovascular trials is preferred.
• Proven ability to perform site visits, SDV, and ensure regulatory compliance.

Responsibilities

• Conduct site visits (initiation, routine monitoring and close-out) to assess study conduct and compliance.
• Verify data accuracy through source data verification (SDV).
• Ensure adherence to protocol, plan, and regulatory requirements (GCP, FDA, ICH).
• Train and support site staff on study procedures and regulatory needs.
• Identify and resolve site-level issues and deviations promptly.
• Manage study supplies and investigational product at sites.
• Prepare monitoring visit reports with findings and action plans.
• Collaborate with data management, regulatory affairs, and project teams.
• Serve as the primary contact for assigned sites.
• Contribute to study-related documents like protocols and CRFs.

Skills

Site monitoring

Communication

Organizational skills

CTMS/EDC proficiency

Travel willingness

Regulatory knowledge

Education

Bachelor's degree in life science or nursing

Master's degree or equivalent experience

Tools

CTMS

EDC systems

Job description

Placements24 seeks a diligent Clinical Research Associate (CRA) to join a cardiovascular trials team in Gauteng. The role centers on monitoring trials to ensure data integrity, patient safety, and regulatory compliance, with a hybrid work model balancing remote monitoring and essential site visits.

The successful candidate will conduct site visits, perform SDV, train site staff, manage trial documents, and collaborate with data management and regulatory teams to support study delivery.