Clinical Trial Manager

hace 1 semana

Barcelona, España Recruiting Erasmus A tiempo completo

**AstraZeneca** is an innovation-driven global biopharmaceutical company focused on the discovery, development and commercialization of prescription medicines, primarily for the treatment of cardiovascular, renal and metabolic, respiratory and immunological, oncological and rare diseases.

In line with our firm commitment to training and developing exceptional talent, this person will join our **Clinical Trial Manager/Clinical and TMF Operations area** to learn and grow through active collaboration with our team.

The Clinical Trial Management (CTM/TMF) team supports Global Clinical Operations across the portfolio throughout the clinical trial life cycle with a focus on planning, implementation, operational execution and inspection readiness of clinical trial activities.

**Conditions**:
**Duration**:1 year

**Hours per day**:Full time

**Location**:Barcelona, Spain

**Training through practical experience**:
The Clinical Trial Management Intern will be an integral part of the Development Operations team. In this role, they will support Clinical Project Leads (CPLs) and Clinical Trial Managers (CTMs) for business administrative tasks, especially for trial master file creation, maintenance, closure, and transfer for a single product and multiple studies per company or CRO SOPs. Assist with centralized business process tasks, e.g., administrative support around meeting management, obtaining insurance documentation, safety letter tracking, CSR appendix generation, and patient safety card procurement and printing to support the study. May assist in the management of all Safety Reports in TMF and Investigator portal systems, including QC, distribution, and tracking.

You will gain experience and participate in:

- Providing support to CTM team members related to day to day work and assisting with organization i.e updates to internal or study related trackers
- Creating, organizing, and standardizing CTM workspaces
- Presenting and tracking status of project activities
- Setting up and participating in career coaching 1:1s.
- Attending functional role related meetings and/or therapeutic area trainings to gain knowledge in rare diseases.
- Assisting with periodic review of study files and for completeness and compliance to the scope of work and standard operating procedures
- May be responsible for performing assigned administrative tasks to support team members with clinical trial activities such as preparation, handling, distribution, filing, and archiving of clinical documentation

**Requirements**:

- Enrolled in an Associates, Bachelors or post graduate degree program.
- Advanced level of spoken and written English.
- Effective communication skills
- the ability to accurately convey information and project objectives to different parts of the business, both written and verbal.
- Microsoft Office Suite skills - Excel, Word, and PowerPoint.
- _

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