Site Activation Intern — Global Health Trials

IQVIA Argentina; Fatih; On-site; TRY 28,000 - 39,000; Full time

Job summary

IQVIA in Turkey offers a 6‑month internship in the Country Site Activation team. Under supervision you will assist regulatory maintenance activities, prepare and review site submissions, and help manage project documentation to support safe clinical trial operations.

You will work with Maintenance Specialists, gain exposure to MOH/EC submissions, and contribute to a global network focused on quality, patient safety, and timely activation of trial sites in a collaborative office environment.

Qualifications

• BSc in Health Sciences or related field, or currently pursuing.
• Strong verbal and written communication.
• Evidence of effective problem solving, analytical, and critical thinking skills.
• Ability to work well in a team and communicate effectively.

Responsibilities

• Work with Maintenance Specialists for preparation, submission, and shipment of Maintenance MOH, EC submissions, and CTA folder preparation.
• Review documents for completeness and accuracy under supervision.
• Prepare site submission documents and review for completeness and accuracy.
• Inform team members of completion of regulatory documents for individual sites.
• Distribute completed documents to sites and internal project team members.
• Update internal systems, databases, tracking tools, timelines and project plans with accurate information.
• Review, track and follow up on progress and approvals of regulatory, ethics, ICs, and IP release documents.

Skills

Communication skills

Problem solving

Teamwork

Education

BSc in Health Sciences

Job description

IQVIA in Turkey offers a 6‑month internship in the Country Site Activation team. Under supervision you will assist regulatory maintenance activities, prepare and review site submissions, and help manage project documentation to support safe clinical trial operations.

You will work with Maintenance Specialists, gain exposure to MOH/EC submissions, and contribute to a global network focused on quality, patient safety, and timely activation of trial sites in a collaborative office environment.