Junior Cta Sponsor Dedicated Barcelona
hace 2 días
TFS is a Global CRO headquartered in Sweden. We genuinely believe that “Global in mind and local at heart” is the core of our success; we operate in a global environment while retaining an in-depth knowledge of regulatory requirements in every country where we operate.
TFS HealthScience are currently recruiting an experienced CTA/Clinical Study Administrator.
**Responsibilities**:
- Assists in coordination and administration of clinical studies from the start-up to execution and close-out.
- Interfaces with Investigators, external service providers and CRAs during the document collection process to support effective delivery of a study and its documents.
- Serves as local administrative main contact and works closely with the CRAs and/or the LSM for the duration of the study.
- Operational responsibility for the correct set-up and maintenance of the local eTMF and ISF including document tracking in accordance with ICH- GCP and local requirements.
- Ensures essential documents under their responsibility are uploaded in a timely manner to maintain the eTMF “Inspection Readiness”.
- Ensures that all study documents are ready for final archiving and completion of local part of the eTMF and supports the CRA in the close out activities for the ISF.
- Contributes to the production and maintenance of study documents, ensuring template and version compliance.
- Sets-up, populates and accurately maintains information in TFS tracking and communication tools (e.g. CTMS such as IMPACT, SharePoint, etc) and supports others in the usage of these systems (with the exception of countries where there is a specific role dedicated to set up and update the systems).
**Requirements**:
- High school/Secondary school qualifications (*),that supports skills and capabilities of the position and ensures successful conduct of responsibilities and appropriate interactions with internal and or external customers.
- At least 1 year of experience working as a CTA.
- Proven organizational and administrative skills.
- Computer proficiency.
- Good knowledge of spoken and written English.
- Working knowledge of the Clinical Study Process and an understanding of the range of working procedures relating to it, together with an understanding of the ICH-GCP guidelines.
- Ability to develop advanced computer skills to increase efficiency in daily tasks.
- Good verbal and written communication.
- Good interpersonal skills and ability to work in an international team environment
**Benefits**:
- The opportunity to be part of a friendly, supportive team and work with exciting technologies
- Competitive salary
- Opportunity to work on a complex trial in challenging therapeutic area
- Private Health Coverage
- Global General Liability Insurance
- Global Travel Insurance
- Flexible working schedule
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