Clinical Trial Site Coordinator Specialist

21 hours ago


Çankaya, Ankara, Turkey Milestone One Full time

Milestone One is a Site Enabling Services organization with global headquarters in Zug, Switzerland. We support trial sites in all related activities according to ICH-GCP and protocol requirements within study-specific defined timelines and enrollment goals.

Key Responsibilities

As a Milestone One Site Coordinator, you will act as the main line of communication between the Sponsor or CRO and the site. This includes ensuring response to feasibility questions are provided in due time, scheduling and preparation for monitoring visits at the medical institution/research center, and being present and available to respond to monitors during all types of monitoring visits conducted at the medical institution.

You will also track patient enrollment and actively support the medical site and CRO/Sponsor team in meeting project timelines and enrollment goals. Additionally, you will maintain study-specific and general tracking of documents at the site level, accurately and timely data entry into study-specific EDC systems, and timely resolution of data clarification queries issued for the site.

Further responsibilities include timely reporting and follow-up on Reportable Adverse Events and Protocol Deviations, proper handling, accountability, and reconciliation of investigational products and clinical supplies, collecting, handling, and maintaining all site-specific regulatory documents as needed, facilitating and supporting contract and budget negotiations at the site level, and supporting Investigator and Site payments and processes as needed.



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