Clinical Trial Coordinator II: Site Activation

Prolific

Quilmes

Hybrid

ARS 69,543,000 - 115,905,000

Full time

5 days ago
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Job summary

Thermo Fisher Scientific in Buenos Aires is seeking a Clinical Trial Coordinator II to provide administrative and technical support to the Project Team. You will oversee trial activities, review regulatory documents, and assist with site activation and study management within SOPs.

The role requires strong organizational skills, excellent English proficiency, and experience with MS Office. Collaboration with global teams and vendors is expected in a fast-paced research environment.

Qualifications

  • Bachelor's degree preferred.
  • High/Secondary school diploma or equivalent required.
  • Excellent English language and grammar skills.
  • Strong organizational skills and attention to detail.
  • Experience with MS Office and data/document management.

Responsibilities

  • Coordinate, oversee and complete trial activities as detailed in the task matrix.
  • Perform file reviews and document findings in appropriate systems.
  • Ensure tasks are completed on time and within budget; communicate risks to leads.
  • Provide administrative support for site activation and regulatory submissions.
  • Maintain site files, ISF/Pharmacy binder materials and related study documents.
  • Support translation materials and translation QC as requested.
  • Train new staff and support process improvements and SOPs.

Skills

Organizational skills
Attention to detail
English proficiency
Communication skills
MS Office

Education

Bachelor's degree preferred
High/Secondary school diploma or equivalent

Tools

MS Office

Job description

Thermo Fisher Scientific in Buenos Aires is seeking a Clinical Trial Coordinator II to provide administrative and technical support to the Project Team. You will oversee trial activities, review regulatory documents, and assist with site activation and study management within SOPs.

The role requires strong organizational skills, excellent English proficiency, and experience with MS Office. Collaboration with global teams and vendors is expected in a fast-paced research environment.

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