Senior Clinical Research Site Monitor & Mentor

IQVIA Argentina; Bloemfontein; On-site; ZAR 400 000 - 600 000; Full time

Job summary

A leading global clinical research provider in Bloemfontein is seeking a qualified Clinical Research Associate to perform site monitoring and manage study compliance. The ideal candidate holds a Bachelor's degree and has at least 4 years of on-site monitoring experience. Strong knowledge of GCP and ICH guidelines is essential. The role offers opportunities for professional growth in a dynamic environment.

Qualifications

• Requires at least 4 years of on-site monitoring experience.
• In-depth knowledge of clinical research regulatory requirements.

Responsibilities

• Perform site monitoring visits as per regulatory requirements.
• Work with sites on subject recruitment plans.
• Evaluate quality and integrity of study site practices.

Skills

On-site monitoring experience

Knowledge of GCP and ICH guidelines

Computer skills (Microsoft Word, Excel, PowerPoint)

Communication skills (English)

Organizational skills

Problem-solving skills

Education

Bachelor's Degree in scientific discipline or healthcare

Job description

A leading global clinical research provider in Bloemfontein is seeking a qualified Clinical Research Associate to perform site monitoring and manage study compliance. The ideal candidate holds a Bachelor's degree and has at least 4 years of on-site monitoring experience. Strong knowledge of GCP and ICH guidelines is essential. The role offers opportunities for professional growth in a dynamic environment.