Associate Clinical Data Manager

hace 3 semanas

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 **Data Management area** to learn and grow through active collaboration with our team.

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

**Hours per day**:Full time

**Location: Barcelona**

**Focus area**:
Associate Clinical Data Manager - Intern is primarily responsible for providing Data Management support to the activities related to clinical studies. May work under direction of an experienced Clinical Data Manager.

**Training through practical experience**:

- Day to day responsibilities may include but are not limited to
- Conducting manual data review for Clinical Data.
- Issuing and closing queries based on manual data review requirements for each assigned study.
- Generating metrics and reports for current state of study database.
- Participating in project team meetings as necessary.
- Provide work status to study Data Management team.
- Reviewing local lab data
- Adhering to Clinical Data Management processes and standards by using implemented systems.
- Highlight potential and technical issues to the Study Data Management team.
- Responsible for the reporting in CDM specified systems and types of deliverables, milestone achievements, risks and mitigations and data transfer agreements, and other study administrative needs.
- Performs User Acceptance Testing of internal and external electronic Data Capture systems as required.
- Provides support to the resolution of issues related to Clinical Data Management deliverables and inputting ideas to help resolve issues and contribute to continuous improvement.
- Performs any CDM related ad-hoc requests from Line Manager or superior.

**Requirements**:

- Knowledge of MS Office is a plus.
- Advanced English (oral and written).
- Attention to detail to ensure quality.
- Good verbal and written skills.
- Ability to work flexibly on simultaneous projects and proactively manage time to meet own deadlines.
- Strong interpersonal skills and ability to communicate effectively in a global environment.
- Good team player.
- Interest on clinical research and clinical trials.
- Interest on Clinical Data Management.

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