Site Activation & Regulatory Specialist

IQVIA; Madrid; Presencial; EUR 32.000 - 52.000; Jornada completa

Descripción de la vacante

IQVIA is seeking a Full-time Site Activation professional in Madrid, Spain. You will act as the primary contact for investigative sites and coordinate with Site Activation Managers and project teams to drive site initiation and activation processes.

The role requires following SOPs, maintaining quality of deliverables, and ensuring timely completion of regulatory and contractual documents. Prior clinical research exposure is recommended to support accurate document handling and timelines.

Formación

• 1 year clinical research experience.

Responsabilidades

• Serve as Single Point of Contact (SPOC) for sites, SAM, and project teams.
• Ensure adherence to SOPs, WIs, and project timelines.
• Perform site activation activities and review regulatory documents.

Conocimientos

SPOC for sites

Site Activation

Regulatory documents handling

Project timelines

Descripción del empleo

IQVIA is seeking a Full-time Site Activation professional in Madrid, Spain. You will act as the primary contact for investigative sites and coordinate with Site Activation Managers and project teams to drive site initiation and activation processes.

The role requires following SOPs, maintaining quality of deliverables, and ensuring timely completion of regulatory and contractual documents. Prior clinical research exposure is recommended to support accurate document handling and timelines.