Regional Medical Director (RMD), Oncology (EU)

TN Italy; Italia; Remoto; EUR 80.000 - 120.000; Tempo pieno

Descrizione del lavoro

Join a forward-thinking company as a Regional Medical Director, where you will play a vital role in oncology clinical sciences. This position offers the opportunity to engage with sites, oversee patient recruitment, and ensure the success of clinical trials across multiple EU countries. With a strong emphasis on relationship-building and communication, you will collaborate with cross-functional teams while traveling up to 65%. If you have an MD and extensive experience in clinical development, this is a chance to make a significant impact in the oncology field.

Competenze

• 8+ years in clinical development, focusing on Oncology, Hematology, and Cardiology.
• Strong understanding of trial conduct and clinical research.

Mansioni

• Engage and train sites through regular meetings and presentations.
• Oversee patient recruitment and address site questions.

Conoscenze

Oncology expertise

Clinical research understanding

Communication skills

Relationship building

Independent work

Formazione

MD

Strumenti

Excel

Word

PowerPoint

Descrizione del lavoro

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Regional Medical Director (RMD), Oncology (EU), Italy

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Client:

TMAC

Location:

Job Category:

-

EU work permit required:

Yes

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Job Reference:

47c8ae7ec79a

Job Views:

2

Posted:

24.04.2025

Expiry Date:

08.06.2025

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Job Description:

The territory includes, but is not limited to, multiple EU countries.

The Regional Medical Director (RMD) is an integral member of the oncology clinical sciences group, responsible for extending clinical sciences across the oncology portfolio at the regional level.

Duties and Responsibilities:

• Site engagement and training: regular touchpoints, meetings, presentations, retraining as needed.
• Recruitment issues: site identification, patient recruitment oversight, troubleshooting.
• Addressing site questions: providing first-line responses, referencing FAQs, and involving Medical Directors as needed.
• Assisting with eligibility assessments and query closure.
• Ensuring sufficient information for safety events and follow-up assessments.
• Handling protocol deviations, retention issues, and missing assessments.
• Collaborating with laboratories and addressing site issues.
• Attending CSTs and weekly meetings with the medical director.
• Providing clinical feedback and support regarding PI interest in local studies.

Qualifications and Experience:

• MD required.
• 8+ years in industry clinical development, with expertise in Oncology, Hematology, and Cardiology.
• Strong understanding of clinical research and trial conduct.
• Excellent relationship-building and communication skills.
• Ability to work independently and in cross-functional teams.
• Fluent in the local language and English.
• Proficient in Excel, Word, PowerPoint.
• Willing to travel up to 65%, including international travel.

Note: If not a passport holder of the country, a work permit may be required. For more info, check our Blog.

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