Orthopedic Surgery Scheduler: Patient Care & Ops

Sourcefit; South Africa; On-site; ZAR 450,000 - 850,000; Full time

Job summary

IQVIA in Bellville, South Africa, is seeking a Senior Site Activation Coordinator to lead country‑level site activation activities, under general supervision, ensuring compliance with local and international regulations, SOPs and study requirements while coordinating with the Site Activation Manager, Project Management and other departments.

You will prepare site documents, review progress, and maintain trackers and timelines, supporting feasibility assessments, regulatory submissions, and

Qualifications

• Bachelor's degree in Life Science or related field.
• Minimum 1 year work experience; experience in healthcare beneficial.
• Good interpersonal, communication and organisational skills to establish and maintain effective working relationships with co-workers, managers and sponsors.
• Strong administration skills.
• Ability to work on multiple projects.

Responsibilities

• Lead country-level site activation activities under general supervision.
• Ensure activities comply with applicable regulations, SOPs, project requirements and budget guidelines.
• Prepare site documents such as questionnaires, CDAs, regulatory and ethics documents and Investigator Pack releases.
• Update and maintain internal systems, databases and tracking tools with project information.

Skills

Interpersonal skills

Organisational skills

Administration skills

Multitasking

Communication

Education

Bachelor's degree in Life Science or related field

Job description

IQVIA in Bellville, South Africa, is seeking a Senior Site Activation Coordinator to lead country‑level site activation activities, under general supervision, ensuring compliance with local and international regulations, SOPs and study requirements while coordinating with the Site Activation Manager, Project Management and other departments.

You will prepare site documents, review progress, and maintain trackers and timelines, supporting feasibility assessments, regulatory submissions, and