Clinical Research Associate II – Greece

Excelya>All job opportunites>Full-time, Permanent Contract>Clinical Research Associate II – Greece

Job description

Excelya is one of the leading independent CRO in Europe. Created in 2014, Excelya is a people-centered Contract Research Organization (CRO) that excels with care.

We offer a personal and authentic experience within a young, ambitious health company on the path to becoming the clinical research leader in Europe thanks to our 900 Excelyates. Our unique one-stop provider service model – leveraging full-service, functional service provider and consulting – allows our Excelyates to evolve through a diverse array of projects. In collaboration with preeminent experts, Excelya advances scientific, managerial and human knowledge to improve the patient journey.

For our team members, excelling with care means benefitting from a stimulating professional environment that encourages personal, intellectual, and operational participation so that together we can be the best in our field. We commit to giving each Excelyate the means to express their natural talents, develop their full potential and invest their unique selves in our unique project.

Excelya is looking to hire a Clinical Research Associate II based in Athens.

What we offer:

  • Quick growth and opportunity for leadership positions – Lead CRA and Managerial roles
  • Highly competitive remuneration package
  • Company car / car allowance
  • Mobile phone/internet
  • Laptop
  • Medical private insurance
  • Food vouchers

Main responsibilities and tasks:

Accompanied by Project Managers, the Clinical Research Associate II will be responsible for the following tasks:

  • Monitoring of international clinical trials on phases I to IV
  • Conduct monitoring of clinical studies
  • Ensure the monitoring and scientific, technical and regulatory quality of international studies
  • Perform investigational product (IP) inventory, reconciliation and reviews storage and security. Verifies the IP has been dispensed and administrated to the subjects / patients according to the protocol. Verifies issues or risks associated with blinded or randomized information related to IP. Applies knowledge of GCP / local regulations and organizational procedures to ensure IP is appropriately re( labelled), imported and released / returned.
  • Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness. Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator / physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations
  • Contribute to the administrative missions required to set up and monitor clinical studies
  • Carry out monitoring and co-monitoring visits with local CRAs to ensure the quality of the data collected, source documents and archiving of investigative documents
  • Interpret the information collected by the various stakeholders in the study and contribute to the implementation of corrective or preventive actions if necessary
  • Be in contact with the study investigators
  • Revise the study sites if necessary
  • Prepare the centers and contribute to the audits and inspections
  • Write visit reports in English
  • Ensure the traceability of the deviations encountered according to a CAPA procedure

Experience and Education:

  • Bachelor’s degree in a life science or any related field
  • Minimum of 1 years’ experience in monitoring activities as a CRA in clinical trials (Phase 2 / Phase 3 studies)
  • Knowledge of Good Clinical Practice / ICH Guidelines and other applicable regulatory timelines
  • Knowledge of the following systems: E-TMF, E-CRF
  • Excellent communication, presentation and interpersonal skills
  • Fluency in written and oral English essential



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