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Clinical Trial Associate

Eingestellt von Michael Bailey Associates - Munich

Gesuchte Skills: Support, Aris, Client

Projektbeschreibung

For our multinational pharma client we are looking for a Clinical Trial Associate (CTA) to assist in the operational and logistic aspects of clinical trials with accordance to ICE-GCP. You will assist in delegated tasks to support the clinical trial team, ensuring that all essential documentation is collected, maintained and filed during the study.

Experience working with Trial Master Files is a must. This is a 16-18 month contract position based in Basel.

Responsibilities:

- Assist in the smooth running of clinical trials; collaborating efficiently with team members to address issues as they aris
- In collaboration with the Trial Document Specialist responsible for setting up and maintaining Trial Master Files and ensuring all relevant study documents are filed and archived based on the appropriate guidelines.
- Manage clinical, regulatory and study-related essential documents such as study protocols, Case Report Forms, Informed Consent Forms etc.; review documents for completeness, accuracy and compliance with protocol and appropriate regulations.
- Interactions with Investigator sites to collect relevant documentation, provide study materials; Liaise with contract organisations, vendors and other suppliers of project support services to ensure study deliverables are met.
- Provide input on agendas, create materials, liaise with meeting planners and coordinate logistics for key meetings.
- Help ensure accuracy of clinical trial management databases and resource/budget tracking tools.
- Assist in the ordering of clinical trial supplies
- Assist in the compilation of the clinical study report and its appendices.
- Audit existing Paper Trial Master Files, collect outstanding documents and archive after study is completed.

Requirements:

-A bachelor's degree or equivalent qualification or work experience in life sciences or nursing.
- Fluent oral and written English
-Previous experience in clinical trials (eg clinical trial design, execution and operations)

Please send CVs or call for more information and a detailed job description.

Michael Bailey International is acting as an Employment Business in relation to this vacancy.

Projektdetails

  • Einsatzort:

    Basel, Schweiz

  • Projektbeginn:

    asap

  • Projektdauer:

    09/2019

  • Vertragsart:

    Contract

  • Berufserfahrung:

    Keine Angabe

Geforderte Qualifikationen

Michael Bailey Associates - Munich