Regional Medical Director (RMD), Oncology, Hematology

The Medical Affairs Company (TMAC); Marseille; Hybride; EUR 125 000 - 150 000; Plein temps

Résumé du poste

A leading medical affairs organization is seeking a Regional Medical Director in Marseille. This role involves engaging and training sites, addressing recruitment issues, and providing clinical assistance in oncology and hematology. The ideal candidate has an MD, 5+ years in clinical development, and excels in communication. This position requires up to 65% travel, including local and international trips.

Qualifications

• 5+ years of industry clinical development experience.
• Strong understanding of the clinical research landscape and trial implementation.
• Proficiency in the local language and English.

Responsabilités

• Engage and train sites.
• Manage protocol deviations.
• Participate in weekly meetings with the medical director.

Connaissances

Oncology expertise

Hematology expertise

Excellent communication

Critical thinking

Problem-solving

Formation

MD

Outils

Excel

Word

PowerPoint

Description du poste

Territory includes but is not limited to: Sites assigned within the EU & Middle East.

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

Duties and Responsibilities :

• Site engagement and training
• Addressing recruitment issues
• Answering questions from sites
• Assisting with eligibility assessments
• Assisting with query closure
• Managing protocol deviations
• Addressing retention issues
• Handling missing assessments
• Laboratory reference range management
• Resolving site issues
• Attending CSTs, if possible
• Participating in weekly meetings or communication with the medical director
• Providing clinical assistance and feedback on PI interest in proposed studies at the local level

Qualifications and Experience :

• MD required
• 5+ years of industry clinical development experience
• Expertise in Oncology and Hematology
• Strong understanding of the clinical research landscape and trial implementation
• Ability to develop and maintain excellent relationships with internal stakeholders, study investigators, and site staff
• Ability to work well in cross-functional and geographically diverse teams
• Excellent communication and independent working skills with scientific/technical personnel
• Strong critical thinking, troubleshooting, and problem-solving skills
• Good initiative and judgment, with the ability to positively represent the company
• Cross-cultural awareness and fluency in the local language of primary country assignment, in addition to English
• Proficiency in Excel, Word, and PowerPoint
• Willingness to travel up to 65%, including local, regional, and international travel
• Valid driver’s license