Empleos actuales relacionados con Freelance Clinical Trial Site Coordinator - Mendoza - Milestone One


  • Mendoza, Mendoza, Argentina PSI CRO A tiempo completo

    Clinical Trial Site Coordinator ResponsibilitiesMain point of contact between Sponsor/CRO and siteEnsure timely response to feasibility questionsSchedule and prepare for monitoring visitsAssist with data entry and trackingReport Adverse Events and Protocol DeviationsManage investigational products and suppliesFacilitate contract and budget negotiations


  • Mendoza, Argentina Milestone One A tiempo completo

    Company Overview:Milestone One is a Site Enabling Services organization with global headquarters in Switzerland. Our mission is to support clinical study sites in stronger study delivery.We understand what clinical study sites need, and we strive to provide exceptional services to our clients.About the Role:The Clinical Trial Site Coordinator will play a...


  • Mendoza, Mendoza, Argentina PSI CRO A tiempo completo

    Job OverviewMilestone One is a Site Enabling Services organization with a global presence.We support clinical study sites in achieving stronger study delivery.


  • Mendoza, Mendoza, Argentina PSI CRO A tiempo completo

    Qualifications and RequirementsCollege degree in Life Science (pharmacy, nursing, lab analytics)Prior experience in clinical trial coordinationAbility to work in fast-paced environmentEffective communication and problem-solving skillsIf you're looking for a dynamic company that values its people, Milestone One may be the right fit.


  • Mendoza, Mendoza, Argentina PSI CRO A tiempo completo

    About the CompanyWe are a leading provider of Site Enabling Services, headquartered in Zug, Switzerland.We understand the needs of clinical study sites and aim to enhance their capabilities.


  • Mendoza, Argentina Solvo Solutions LLC A tiempo completo

    Job Overview:Solvo Solutions LLC is seeking an experienced Clinical Operations Coordinator to manage medical records and ensure seamless communication with healthcare providers.Responsibilities:Manage medical records, including setup, reminders, and updates.Coordinate with healthcare providers to obtain medical records and bills.Prepare medical recaps and...

  • Purchasing Supervisor

    hace 7 días


    Mendoza, Argentina Flowserve Corporation A tiempo completo

    Company Overview: If a culture of excellence, innovation and ownership is what you’re searching for, consider putting your experience in motion at Flowserve. As an individual contributor, or as a leader of people, your enterprise mindset will ensure Flowserve’s position as the global standard in comprehensive flow control solutions. Here, your...

Freelance Clinical Trial Site Coordinator

hace 1 semana


Mendoza, Argentina Milestone One A tiempo completo

Milestone One is a Site Enabling Services organization with global headquarters in Zug, Switzerland.
We understand what clinical study sites need and our overall mission is to support sites in stronger study delivery.

Please submit CV in English. Job DescriptionMilestone One Site Coordinator supports trial sites in all related activities according to ICH-GCP, protocol requirements within study specific defined timelines and enrollment goals.
In this role you will:
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.QualificationsCollege or university degree in Life Science, preferably in pharmacy, nursing or lab analytics.Prior experience in coordinating clinical trials on site.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.Additional InformationIf 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.

#J-18808-Ljbffr