Senior Clinical Research Associate (sCRA)

Planet Pharma Staffing Limited; Italia; Remoto; EUR 50.000 - 75.000; Tempo pieno

Descrizione del lavoro

A leading Contract Research Organization seeks a Senior Clinical Research Associate in Italy. The role offers an opportunity to work remotely on impactful oncology studies in a supportive environment, requiring significant CRA experience and a Ministerial Decree certification. Join a team committed to high-quality clinical practices and innovation.

Servizi

Competitive compensation and benefits package

Flexibility of remote work

Long-term career development opportunities

Competenze

• Proven experience as a CRA within a CRO environment.
• Oncology experience is essential.
• Ability to work independently in a remote setting.

Mansioni

• Perform and coordinate all aspects of the clinical monitoring process.
• Conduct 5–8 monitoring visits per month across multiple sites.
• Provide guidance and mentorship to junior CRAs.

Conoscenze

Communication skills in Italian

Communication skills in English

Organizational skills

Time-management skills

Formazione

Ministerial Decree certification

Strumenti

CTMS

eTMF

IXRS

EDC platforms

Descrizione del lavoro

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 Pharmais 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 aSenior CRAto 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 validMinisterial Decreecertification 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 todayor reach out to us directly for a confidential chat.