Company Overview

We are the company that cares – for our staff, our clients, our partners, and the quality of our work. Founded in 1995, our global team of over 2,800 driven individuals operates at the forefront of medical science, changing lives with new medicines.

Job Description

Join our international team and be the key support to clinical research projects, enhancing communication and managing essential documents and information.

Only CVs in English will be accepted.

Key Responsibilities

• Primary contact between site personnel and CRA for query resolution and EDC completion.
• Manage vendor communication, study supplies, and access management.
• Ensure completion of pre-study testing of local site facilities.
• Assist Monitors with subject and site event information in CTMS.
• Oversee order, receipt, and reconciliation of clinical supplies.
• Ensure compliance with regulatory and ethics committee submissions.
• Coordinate site audits and inspections.
• Manage TMF at the site and country level, updating Investigator Site Files (ISF).
• Facilitate project training for site teams.
• Review document management and translations status.
• Ensure safety information flows to investigative sites.

Qualifications

• Degree in Life Sciences.
• Experience in administrative roles, preferably in international settings.
• Prior experience as a CTA for CROs.
• Experience in Clinical Research.
• Knowledge of local regulations.
• Full proficiency in English.
• Proficiency in MS Office.
• Ability to plan and work in a dynamic team.
• Strong communication and collaboration skills.

Additional Information

Advance your career in clinical research by coordinating a variety of tasks and learning new skills while growing with the company.