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Senior Clinical Research Associate
Michael PageIstanbul, TR30+ gün önce
İş tanımıPerforming 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!
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Clinical Associate • Istanbul, TR