Regional Medical Director (RMD), Oncology (EU)

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Regional Medical Director (RMD), Oncology (EU)

Client:

The Medical Affairs Company

Location:

Remote, Italy

Job Category:

Oncology

EU work permit required:

Yes

Job Reference:

b3af3442bf8d

Job Views:

3

Posted:

24.03.2025

Expiry Date:

08.05.2025

Job Description:

Regional Medical Director (RMD), Oncology (EU)

The Regional Medical Director (RMD) is an integral member of the oncology clinical sciences group, who assists and extends Clinical Sciences across the oncology portfolio on assigned studies at the regional level.

Duties and Responsibilities:

1. Site engagement and training: Regular touchpoints with sites, meeting with sites and presenting at PSVs, SIVs, and retraining as needed.
2. Recruitment issues: Site identification/recruitment, addressing patient recruitment challenges in collaboration with CTL.
3. Answering questions from sites: Addressing straightforward medical/clinical questions and coordinating responses with the Medical Director.
4. Assisting with eligibility assessments: Performing eligibility checks and addressing urgent eligibility questions.
5. Assisting with query closure: Helping sites understand what is needed to close medical queries and ensuring all necessary information is gathered.
6. Protocol Deviations: Retraining sites to prevent future deviations in collaboration with CTL.
7. Retention issues: Ensuring sites follow up with patients and meet protocol-specific requirements.
8. Missing assessments: Assisting in obtaining key missing assessments in collaboration with CRA/CTL.
9. Laboratory reference range: Ensuring laboratory reference ranges are provided for local lab data.
10. Site issues: Discussing potential quality issues with sites and involving the global medical director if needed.
11. Attend CSTs and maintain weekly communication with the medical director.
12. May provide clinical assistance and feedback on PI interest in proposed studies at the local level.

Qualifications and Experience:

1. MD required
2. 8+ years of industry clinical development experience.
3. Expertise in Oncology, Hematology, and Cardiology.
4. Strong understanding of clinical research landscape and implementation of clinical trials.
5. Demonstrated ability to develop and maintain excellent working relationships with stakeholders.
6. Ability to work well in cross-functional and geographically diverse teams.
7. Excellent oral presentation skills and ability to communicate independently.
8. Critical thinking and problem-solving skills.
9. Cross-cultural awareness and fluency in the local language of primary country assignment in addition to English.
10. Computer skills including Excel, Word, and PowerPoint.
11. A willingness to travel up to 65%.
12. Valid driver’s license.