Clinical Research Specialist

il y a 2 semaines


Paris, Île-de-France Excelya Temps plein

Clinical Research Role at Excelya

We are seeking a Clinical Scientist to join our team at Excelya, a people-centered Contract Research Organization (CRO). In this role, you will support and represent the Study Medical Manager in all oncology study-related activities from set up to closure.

Key Responsibilities:

  • Contribute to the elaboration of trial documents, including abbreviated protocols, informed consent forms, and medical data validation plans.
  • Review medical data on patient profiles, listings, and CIOMs.
  • Collaborate with Trial Operations, pharmacovigilance, and statistics teams for listing establishment and data consistency review.
  • Review study-related documents, including CRFs, completion instructions, and deviations lists.
  • Contribute to the review of interim and final study reports, associated statistical tables, and draft publications.
  • Medical review of files and contribution to clinical study management, including protocol writing, basic clinical analysis, and medical training.

Requirements:

  • Senior global project managers, PhDs, or PharmDs with clinical research experience.
  • Experience in GCP and reviewing patient profile data.
  • 4-7 years of experience.
  • Working language and document writing in English.


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