Site Coordinator

PSI CRO · psi-cro.com

Olsztyn, Warmian-Masurian Voivodeship, Poland Full-time 2 days ago
Workplace
On-site
Location
Olsztyn, Warmian-Masurian Voivodeship, Poland
Who can apply
Based in Poland: you usually need the right to work there

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About the role

Job Description

The Milestone One Site Coordinator role supports a Clinical Study Site in clinical trial related activities according to ICH-GCP, protocol requirements within Study specific defined timelines and enrollment goals.

The function of the role may include, but not limited to, any/all of the following:

* Act as the main line of communication between the Sponsor or CRO and the site. * Ensure response to feasibility questions are provided in due time. * Assist in scheduling and preparation for all types of monitoring visits at the medical institution/research center. * Be present and available to respond to monitors during all types of monitoring visits conducted at the medical institution. * Track patient enrollment and actively support the medical site and CRO/Sponsor team in meeting project timelines and enrollment goals. * Maintain study specific and general tracking of documents at the site level. * Accurate and timely data entry into study specific EDC systems and timely resolution of data clarification queries issued for the site. * Timely reporting and follow up on Reportable Adverse Events and Protocol Deviations. * Proper handling, accountability and reconciliation of investigational products and clinical supplies. * Collect, handle and maintain all site-specific regulatory documents as needed. * Facilitate and support the contract and budget negotiations at the site level. * Support Investigator and Site payments and processes as needed. * Schedule and/or perform study procedures as per study requirements and delegation of responsibilities. * Prepare for and participate in onsite study audits or regulatory agency inspections.

Qualifications

* A university degree in Life Science, preferably in pharmacy, nursing or lab analytics. * Minimum of 2 years of on-the-job experience as a site coordinator * Ability to work in a fast-paced environment, with short timelines and multiple tasks to be completed simultaneously. * Ability to effectively communicate in stressful situations and demonstrate the ability to problem-solve in an effective and efficient manner. * Flexibility in working hours may be required depending on the schedule of study procedures and/or patient visits. * Fluent Polish and English

Additional Information

If you feel it is time to make your skills and knowledge visible within a developing company with true focus on its people, then Milestone One is the right choice for you.

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