Global Site Activation Analyst

hace 2 días

Buenos Aires, Argentina IQVIA A tiempo completo

**Location**: Argentina / Brazil / Chile / Colombia / Mexico
- *_**_Please send your CV in English_**_*_

The Global Site Activation unit within IQVIA has the vision to be the clear market leader in clinical trial site activation driving best in class employee, site and customer experiences, and industry-leading outcomes and we look for passionate people to join our team.

The** Global Site Activation Analyst** is a Project Coordinator during Start-up & Maintenance Phase and plays an important role in the management and delivery of site selection, activation, maintenance and regulatory activities for selected studies or multi-protocol programs, working in close collaboration with the Global Site ID Lead, Site Activation Manager, Maintenance Lead and Country teams.

**Essential Functions**:

- Responsible for study knowledge retention throughout the life-cycle of the study.
- Support the delivery of our clinical trial portfolio and belongs to a global unit with vast career growth opportunities.
- Perform start up and site activation activities according to applicable regulations, SOPs and work instructions. Distribute completed documents to sites and internal project team members.
- Support, setup and maintenance of various clinical systems
- Analyze data & monitor study metrics and compliance
- Prepare project status reports and presentation materials for internal project team and customer meetings
- Highly proficient in data extraction and report generating tools and extend support to stakeholders based on their needs
- Support study teams in timelines projection for start-up & maintenance activities
- Support project finance/EAC analysis
- Escalate quality or compliance issues, delays, risks in meeting project timelines to relevant stakeholders

**Qualifications**:

- Bachelor´s degree in Life Science or related field.
- Minimum 3 years of relevant experience in clinical, healthcare and/or Pharma companies.
- Good knowledge of clinical research domain and applicable regulatory requirements/ guidelines
- Good knowledge of Clinical Systems (CTMS, TMF, Workflows etc)
- Advanced English level is mandatory.
- Strong Analytical skills
- Strong communication and collaboration skills
- Good Project Management Skills
- Proven ability to establish and maintain effective working relationships with co-workers and managers across the globe.
- Demonstrable experience working on multiple projects/tasks balancing competing priorities.
- Understanding of study financial management would be an advantage.

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