Key Responsibilities:

• Provide clinical development and indication expertise specific to the country/cluster.
• Validate study designs, contribute to the start-up phase, provide robust training to clinical operations teams and support recruitment and trial awareness.
• Offer clinical/medical expertise for IRB/EC interactions and informed consent forms.
• Interact with external experts, regulatory authorities, and patient advocacy groups.
• Leverage innovation in clinical trial planning and recruitment strategies.
• Support internal stakeholders and decision boards regarding clinical trials.
• Review and resolve trial-related scientific/clinical/medical issues and support protocol deviations.

Essential Requirements:

• Scientific degree M.D., Ph.D., or Pharm.D. (M.D. highly desirable) - Subspecialty training desirable
• 3 years of clinical development experience in the pharmaceutical industry or clinical practice.
• Ability to manage a study from the scientific/medical/clinical perspective, and a demonstrated capability to problem solve and mediate complex scientific/clinical/medical/operational issues.
• Ability to lead effectively by communicating well, motivating a cross-functional team, and handling and delegating responsibilities.
• Agility to move quickly across different therapeutic areas and indications.
• Demonstrated problem-solving skills and comfort with complexity.
• Ability to prepare and deliver high quality presentations.

Desirable Requirements:

• Sound understanding of the overall clinical development process, and ICH/GCP principles.
• Speaks and writes English, French desirable