Portugal Site Activation Specialist - Drive Clinical Trial

Iqvia Llc

Lisboa

Presencial

EUR 38 000 - 60 000

Tempo integral

14 dias+
Gerador de candidaturas

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Resumo da oferta

IQVIA's Global Site Activation team in Portugal seeks a Site Activation Specialist to support feasibility, site activation and maintenance activities within assigned studies.

You will review regulatory documents, coordinate with the Site Activation Manager, Project Management and sponsors, and maintain timelines and data in internal systems.

Join a global network delivering high-quality site activation to ensure patient access to clinical trials and innovative therapies.

Qualificações

  • Bachelor's Degree in Life Science or related field.
  • Minimum of 3 years' prior experience in Clinical Research.
  • Experience with submissions to Ethics Committees and Regulatory Authorities, contract and budget negotiations, study start-up activities, and overall site activation processes.
  • Ability to work independently but also collaborate with others.

Responsabilidades

  • Serve as a Single Point of Contact to perform feasibility, site activation and some maintenance activities in assigned studies.
  • Review documents for completeness, consistency, and accuracy, and maintain project timelines and data in internal systems.
  • Inform team members of completion of regulatory contractual documents and distribute them to sites and project teams.
  • Track progress and follow up on required documents (ethics, regulatory, consent forms) and ensure timely approvals.

Conhecimentos

Interpersonal skills
Communication
Organisational skills
Team collaboration
Independent work

Formação académica

Bachelor's Degree in Life Science or related field

Descrição da oferta de emprego

IQVIA's Global Site Activation team in Portugal seeks a Site Activation Specialist to support feasibility, site activation and maintenance activities within assigned studies.

You will review regulatory documents, coordinate with the Site Activation Manager, Project Management and sponsors, and maintain timelines and data in internal systems.

Join a global network delivering high-quality site activation to ensure patient access to clinical trials and innovative therapies.

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