Clinical Trial Support Specialist

Pharmaxi LLC.

Warszawa

Ibrido

PLN 60.000 - 80.000

Tempo pieno

6 giorni fa
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Descrizione del lavoro

Pharmaxi LLC. is seeking a Clinical Trial Assistant to support day-to-day organisation of clinical trials within a CRO environment. You will assist with project documentation, coordinate meetings, and ensure regulatory and site communications run smoothly.

Ideal candidates are accurate, well organised, with English able to work with documentation, and eager to learn. This role offers growth in clinical research and exposure to national and international projects.

Competenze

  • Interest in clinical trials and development in the area of clinical research.
  • Very good work organisation and attention to detail.
  • Ability to work with documents and deadlines.
  • Communication skills and readiness to cooperate with different team members.
  • Knowledge of English sufficient to work with documentation.
  • Responsibility, accuracy and willingness to learn.

Mansioni

  • Administrative and operational support for the clinical trial team.
  • Preparing, completing and organising project documentation.
  • Cooperation with CRA, Project Manager, regulatory affairs and data management departments.
  • Supporting communication with investigational sites, sponsors and project partners.
  • Assistance in organising meetings, training sessions, visits and project activities.
  • Monitoring deadlines, task lists and document status.
  • Supporting the preparation of documentation for archiving.

Conoscenze

Clinical trials
Documentation
Communication
Organisational skills

Formazione

Education related to medical/pharmaceutical/biological sciences

Descrizione del lavoro

Pharmaxi LLC. is seeking a Clinical Trial Assistant to support day-to-day organisation of clinical trials within a CRO environment. You will assist with project documentation, coordinate meetings, and ensure regulatory and site communications run smoothly.

Ideal candidates are accurate, well organised, with English able to work with documentation, and eager to learn. This role offers growth in clinical research and exposure to national and international projects.

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