Clinical Trial Associate - 3 months
Michael Page Switzerland
Infos sur l'emploi
- Date de publication :18 septembre 2024
- Taux d'activité :100%
- Type de contrat :Temporaire
- Lieu de travail :Genève
This 3-month contract role involves supporting the Clinical Project Manager with administrative tasks related to clinical trial operations, including maintaining inspection-ready Trial and Sponsor Master Files and ensuring accurate document management in the eTMF.
Our client is a fast-growing medical device company.
Description
- Support the Clinical Project Manager with administrative tasks related to clinical operations, including essential document signatures and coordination.
- Help establish and maintain the Trial Master File (TMF) in a constant inspection-ready state.
- Ensure timely and accurate quality control (QC) of clinical trial documents, with proper filing in the electronic Trial Master File (eTMF).
- Assist in maintaining the Sponsor Master File, ensuring it remains compliant and inspection-ready.
- Coordinate and manage the preparation and shipping of study materials and essential documents.
- Collaborate with the Clinical Project Manager to ensure full adherence to internal SOPs, policies, local regulatory requirements, and department processes.
Profile
- High School Diploma or Bachelor's degree in Life Sciences preferred.
- Minimum of 2 years of clinical trial experience, ideally in the medical device or pharmaceutical industry.
- Proficiency with Microsoft Office and similar technology tools.
- Strong organizational skills and attention to detail.
- Fluent in both French and English.
Job Offer
This is a great opportunity to gain hands-on experience in clinical operations within a dynamic team. If you're detail-oriented, proactive, and ready for a challenge, this could be the role for you!
Contact
Michael Page Switzerland