Senior Oncology Research Manager

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

Descrizione del lavoro

Join a leading company in clinical research as a Senior Clinical Research Associate. In this role, you'll manage the monitoring process for oncology studies, collaborate with teams, and ensure regulatory compliance. This position offers flexibility, competitive compensation, and opportunities for career development.

Servizi

Competitive compensation and benefits

Flexible remote work

Career development opportunities

Competenze

• Proven track record as a CRA, preferably in a CRO environment.
• Strong oncology experience.
• Excellent communication skills in Italian and English.

Mansioni

• Managing the clinical monitoring process across multiple sites.
• Conducting on-site or remote visits.
• Ensuring data integrity and compliance with regulations.

Conoscenze

Clinical Research

Communication

Monitoring

Oncology

Formazione

Valid Ministerial Decree certification

Strumenti

CTMS

eTMF

IXRS

EDC platforms

Descrizione del lavoro

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Senior Clinical Research Associate Job Description

We are seeking a highly skilled Senior Clinical Research Associate to join our team. As a key member of our clinical operations group, you will be responsible for managing the monitoring process across multiple sites in Italy.

The ideal candidate will have a strong background in clinical research and experience working as a CRA within a Contract Research Organization (CRO) environment. You will be proficient in clinical systems including CTMS, eTMF, IXRS, and EDC platforms, and possess excellent written and verbal communication skills in both Italian and English.

Key responsibilities include:

• Performing and coordinating all aspects of the clinical monitoring process in accordance with ICH-GCP guidelines, local regulations, and company SOPs.
• Conducting 5–8 on-site or remote monitoring visits per month across multiple sites in Italy.
• Ensuring the integrity of clinical data and proper site management throughout the duration of the study.
• Collaborating with cross-functional teams to ensure study milestones are achieved on time.
• Providing guidance and mentorship to junior CRAs as needed.

To be successful in this role, you will require:

• A proven track record of 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.

Benefits of this role include:

• Working on high-impact oncology studies with a passionate and collaborative team.
• Enjoying the flexibility of remote work, coupled with long-term career development.
• Competitive compensation and benefits package.

This is an exciting opportunity to take your career to the next level and make a meaningful contribution to our team. If you are a motivated and experienced professional looking for a new challenge, we encourage you to apply.