Remote Senior Clinical Trial Manager - Oncology (Europe)

Worldwide Clinical Trials; Italia; Remote; EUR 90,000 - 120,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Senior Clinical Trial Manager for a remote Europe role. You will lead clinical site management from startup through closeout, partnering with project management to drive monitoring strategies and ensure quality and regulatory compliance across oncology studies.

You will mentor CRAs and site teams, manage risks, and coordinate sponsor interactions, audits, and inspections, all while maintaining high-quality study documentation and trial master file standards.

Qualifications

• Four-year college with major in biological, physical or health studies and 4+ years as a Senior CRA or equivalent.
• Alternatively, two-year college with nursing or life science degree and 6+ years as a CRA.
• Minimum 2 years as CTM/LCRA overseeing a CTM team.

Responsibilities

• Lead clinical site management from startup to closeout across studies and regions.
• Develop monitoring strategies with project management to meet goals.
• Provide leadership to CRAs and site management across regions.
• Represent sponsors and study teams in audits, inspections and key meetings.
• Oversee QA by monitoring activities and protocol deviation reviews.
• Track study metrics, recruitment, resources and risks; implement solutions.
• Support patient recruitment and site-specific recruitment strategies.
• Ensure Trial Master File quality and timely documentation review.

Skills

Leadership of remote teams

Project management

Regulatory knowledge

Clinical trial oversight

Communication skills

Education

Four-year college major in biological/health studies

Two-year college education in life sciences (preferred)

Tools

CTMS

EDC

IxRS/IVRS

eCRF platforms

Job description

Worldwide Clinical Trials is seeking a Senior Clinical Trial Manager for a remote Europe role. You will lead clinical site management from startup through closeout, partnering with project management to drive monitoring strategies and ensure quality and regulatory compliance across oncology studies.

You will mentor CRAs and site teams, manage risks, and coordinate sponsor interactions, audits, and inspections, all while maintaining high-quality study documentation and trial master file standards.