Clinical Site Lead (Foz)

Clinical Site Lead (Foz)

10 sep
|
GForce Life Sciences
|
Foz

10 sep

GForce Life Sciences

Foz

Clinical Site Lead (EMEA)
La experiencia que se espera de los solicitantes, así como las habilidades y cualificaciones adicionales necesarias para este trabajo, se enumeran a continuación.
Role Summary
The Clinical Site Lead drives study execution, operational excellence, and site management across multiple therapy areas in accordance with local and international regulations. This role is a recognized subject matter expert in clinical working instructions, clinical investigation plans, and product/disease state throughout the full study lifecycle, from startup through closeout.
Key Responsibilities
- Acts as the primary point of contact, internally and externally, for assigned study sites.
- Coordinates, implements, and executes clinical studies within assigned country/region.
- Identifies, develops, and maintains sites capable of delivering startup goals, study participation levels, and required data quality.
- Identifies appropriate investigators, completes qualification processes, and establishes site/sponsor expectations for study execution.




- Facilitates all aspects of the site startup process, coordinating with Site Operations teams to ensure activation and enrollment within timelines.
- Develops site-specific strategies to promote appropriate patient enrollment.
- Attends study procedures and follow-ups as required per study-specific requirements.
- Monitors clinical studies at sites to ensure compliance with applicable regulatory requirements, Good Clinical Practice, and accuracy standards, including initiation, periodic, and closeout visits.
- Reviews data and source documentation from investigational sites for accuracy and completeness; provides timely feedback to sites.
- Leads, initiates, and coordinates activities to ensure clinical study and regulatory compliance, including Key Compliance Indicator reporting and audit support.
- Ensures adverse events, device complaints, and protocol deviations are reported in a timely manner per regulations and standa

📌 Clinical Site Lead (Foz)
🏢 GForce Life Sciences
📍 Foz

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