This job offer is not available in your country.

Senior Clinical Research Associate

Michael PageIstanbul, TR

30+ days ago

Job description

Performing site selection, initiation, monitoring and close-out visits

Supporting the development of a subject recruitment plan

Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution

Collaborating with experts at study sites and with client representatives

Array

University degree in a scientific discipline or health-related field
At least 2 years of independent on-site monitoring experience
Solid understanding of ICH-GCP guidelines and local regulatory landscape
Proficiency in Microsoft Office applications
Excellent command of Turkish and English
Strong communication, organizational, and problem-solving skills
Ability to establish effective working relationships with site staff, colleagues, and sponsor contacts
Willingness to travel; valid driver's license
We are supporting a leading global clinical research organization in their search for an experienced Senior Clinical Research Associate to lead site monitoring and clinical operations in Turkey.

If you are passionate about clinical research and seeking a rewarding opportunity in Istanbul, we encourage you to apply today!

Create a job alert for this search

Clinical Associate • Istanbul, TR