Oncology Clinical Research Associate - Sponsor Monitoring

IQVIA; Centurion; On-site; ZAR 500 000 - 700 000; Full time

Job summary

A global clinical research organization seeks a Site Monitor to ensure adherence to study protocols in oncology clinical trials. Candidates must hold a Bachelor’s degree in a scientific discipline and have at least 2-3 years of on-site monitoring experience. Key responsibilities include conducting monitoring visits, managing regulatory submissions, and ensuring quality site practices. Strong communication and organizational skills are essential, as well as proficiency in Microsoft Office tools. This role contributes to improving patient outcomes and population health globally.

Qualifications

• At least 2-3 years of on-site monitoring experience.
• Good knowledge of clinical research regulatory requirements.
• Experience in Inflammatory Bowel Disease (IBD) is an advantage.

Responsibilities

• Perform site monitoring visits including selection, initiation, and close-out.
• Work with sites to track subject recruitment plan.
• Administer protocol training to assigned sites.

Skills

Oncology experience

Communication skills

Organizational skills

Problem-solving skills

Time management

Computer proficiency

Education

Bachelor's Degree in scientific discipline or health care

Tools

Microsoft Word

Excel

PowerPoint

Job description

A global clinical research organization seeks a Site Monitor to ensure adherence to study protocols in oncology clinical trials. Candidates must hold a Bachelor’s degree in a scientific discipline and have at least 2-3 years of on-site monitoring experience. Key responsibilities include conducting monitoring visits, managing regulatory submissions, and ensuring quality site practices. Strong communication and organizational skills are essential, as well as proficiency in Microsoft Office tools. This role contributes to improving patient outcomes and population health globally.