Senior CRA

JR Italy; Latina; Remoto; EUR 40.000 - 60.000; Tempo pieno

Descrizione del lavoro

A leading global Clinical Research Organization is seeking a Senior Clinical Research Associate to join their remote team in Italy. This role involves coordinating clinical studies primarily in oncology, offering flexibility and support in a dynamic environment. The ideal candidate will have proven CRA experience, strong communication skills, and must hold valid certification for monitoring activities in Italy. Apply today for an opportunity that promises stability and professional growth.

Servizi

Competitive compensation and benefits

Career development opportunities

Work flexibility

Competenze

• Experience as a CRA, preferably in CRO.
• Proficiency in oncology essential.
• Excellent English and Italian communication skills.

Mansioni

• Coordinate clinical monitoring processes as per guidelines.
• Conduct monitoring visits across sites in Italy.
• Mentor junior CRAs and manage study milestones.

Conoscenze

Clinical Systems Proficiency

Communication

Time Management

Organization

Formazione

Ministerial Decree Certification

Strumenti

CTMS

eTMF

IXRS

EDC platforms

Descrizione del lavoro

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Senior Clinical Research Associate (CRA) – Italy (Remote, Permanent)

Location: Italy (Remote)

Employment Type: Permanent

Industry: Clinical Research / Life Sciences

Sector: Contract Research Organization (CRO)

Planet Pharma is proud to partner with a global, full-service Contract Research Organization that is dedicated to delivering high-quality, innovative solutions to the world’s leading life science companies. With a strong reputation for operational excellence and patient-focused research, our client is expanding their experienced clinical team in Italy and is looking for a Senior CRA to join their remote team.

This is a fantastic opportunity for an experienced CRA to step into a reputable, full-service role within a dynamic and supportive environment. You'll have the chance to work on cutting-edge clinical studies, primarily in oncology, while enjoying the flexibility of remote work and the backing of a world-class CRO.

Key Responsibilities:

• Perform and coordinate all aspects of the clinical monitoring process in accordance with ICH-GCP guidelines, local regulations, and company SOPs.
• Conduct 5–8 on-site or remote monitoring visits per month across multiple sites in Italy.
• Ensure the integrity of clinical data and proper site management throughout the duration of the study.
• Collaborate with cross-functional teams to ensure study milestones are achieved on time.
• Provide guidance and mentorship to junior CRAs as needed.
• Communicate effectively with site staff and internal project teams.

Requirements:

• Proven experience working as a CRA, preferably within a CRO environment.
• Proficiency in clinical systems including CTMS, eTMF, IXRS, and EDC platforms.
• Oncology experience is essential – candidates without it will not be considered.
• Must hold valid Ministerial Decree certification to conduct monitoring activities in Italy.
• Excellent written and verbal communication skills in both Italian and English.
• Strong presentation, organizational, and time-management skills.
• Ability to work independently in a remote setting while managing multiple priorities.

Why Apply?

• Be part of a globally respected CRO with a strong pipeline and a commitment to innovation.
• Work on high-impact oncology studies with a passionate and collaborative team.
• Enjoy the flexibility of remote work, coupled with long-term career development.
• Competitive compensation and benefits package.

If you are ready to take the next step in your CRA career and are looking for a role that offers stability, growth, and purpose, apply today or reach out to us directly for a confidential chat.