Regional Medical Director (RMD), Oncology, Hematology

The Medical Affairs Company (TMAC); Nice; Sur place; EUR 85 000 - 120 000; Plein temps

Résumé du poste

A leading medical affairs firm is seeking a Regional Medical Director in Nice, France. This role involves engaging with clinical sites, assisting with recruitment and eligibility assessments, and contributing to the development of oncology and hematology studies. Candidates must hold an MD and have over 5 years of clinical development experience, along with the ability to travel up to 65%. A strong understanding of clinical trials and cross-functional teamwork is essential.

Qualifications

• 5+ years of industry clinical development experience.
• Demonstrated ability to develop and maintain relationships with stakeholders.
• Fluent in local language of assignment and English.

Responsabilités

• Engage with sites and train staff.
• Assist with recruitment and eligibility assessments.
• Attend CSTs and communicate with medical director regularly.

Connaissances

Oncology expertise

Hematology expertise

Cross-functional teamwork

Oral presentation skills

Problem-solving skills

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, 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
• Recruitment issues
• Answering questions from sites
• Assisting with eligibility assessments
• Assisting with query closure
• Protocol Deviations
• Retention issues
• Missing assessments
• Laboratory reference range
• Site issues
• Attend CSTs, if possible
• Weekly meetings with medical director (if possible) or weekly communication with medical director, at a minimum
• May provide 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, Hematology
• Strong understanding of clinical research landscape and implementation and conduct of clinical trials
• Demonstrated ability to develop and maintain excellent working relationships with both internal stakeholders and study investigators and site staff
• Demonstrated ability to work well in cross-functional and geographically diverse teams
• Ability to communicate and work independently with scientific/technical personnel with excellent oral presentation skills
• Ability to think critically, and demonstrated troubleshooting and problem-solving skills
• Excellent initiative and judgment, and demonstrated ability to positively represent Regeneron in a compliant manner
• Cross-cultural awareness and fluent in the local language of primary country assignment in addition to English
• Computer skills including Excel, Word, and PowerPoint
• A willingness to travel up to 65%, which may include local, regional, and international travel
• Valid driver’s license