Global Clinical Site Lead - Remote & Travel

GForce Life Sciences; España; Presencial; EUR 90.000 - 120.000; Jornada completa

Descripción de la vacante

GForce Life Sciences seeks a Clinical Site Lead to drive study execution, site management, and regulatory compliance across multiple therapy areas. You will act as the primary contact for assigned sites, coordinate studies within the region, identify capable sites, and establish expectations with sponsors to ensure quality delivery.

Requirements include 4+ years in clinical research or site management, fluency in English and local languages, expert GCP knowledge, and the ability to travel

Formación

• Background in engineering, science, health science, nursing, or a related field; or equivalent experience in clinical research.
• Minimum 4 years of relevant experience in clinical research and/or clinical site management.
• Fluency in English (written and verbal) and local/country language.
• Proficiency in MS Office and clinical database systems (Oracle preferred).
• Expert knowledge of GCPs and regulatory compliance guidelines for clinical trials (ISO standards, FDA regulations).
• Expert knowledge of clinical study conduct, follow-up, and monitoring.
• Advanced knowledge of clinical and outcomes research study design.
• Strong communication, prioritization, organizational, and time management skills.
• Ability to travel at least 70%, including internationally.

Responsabilidades

• Acts as the primary point of contact for assigned study sites.
• Coordinates, implements, and executes clinical studies within the region.
• Identifies, develops, and maintains sites capable of startup goals and data quality.
• Establishes site/sponsor expectations for study execution.
• Facilitates site startup, activation, and enrollment within timelines.
• Develops site-specific strategies to promote patient enrollment.
• Monitors sites to ensure regulatory compliance and data accuracy.
• Reviews data and source documentation for completeness and quality.
• Leads activities to ensure regulatory compliance and audit support.
• Ensures adverse events and protocol deviations are reported timely.
• Trains site personnel on protocol and regulations.
• Provides progress updates to Clinical Operations and Study Management.
• Contributes to site budget discussions and contract coordination.

Conocimientos

Engineering/Science background

Regulatory compliance knowledge

GCP knowledge

Clinical study management

MS Office proficiency

Oracle clinical DB experience

Travel readiness

Excellent communication

Educación

Engineering/Science/Health science background or equivalent

Herramientas

Oracle Clinical Database

Descripción del empleo

GForce Life Sciences seeks a Clinical Site Lead to drive study execution, site management, and regulatory compliance across multiple therapy areas. You will act as the primary contact for assigned sites, coordinate studies within the region, identify capable sites, and establish expectations with sponsors to ensure quality delivery.

Requirements include 4+ years in clinical research or site management, fluency in English and local languages, expert GCP knowledge, and the ability to travel