Director of Training – Global Medical Affairs

atKyverna TherapeuticsRemoteUS flagUnited StatesFull-timeDirectorLead$210k – $245k/year

Posted Aug 10

This is a fully remote position, open to applicants in United States.

πŸ“‹ Description

β€’ Create and implement a comprehensive global training strategy designed for cell therapy initiatives throughout their clinical and commercial phases.

β€’ Develop onboarding, certification, and ongoing learning pathways specific to roles within the Medical and Commercial teams.

β€’ Design and produce training materials while managing and utilizing external vendors effectively.

β€’ Conduct training sessions focused on disease state awareness, unmet medical requirements, CAR T product development and manufacturing, clinical data analysis, safety monitoring and management, as well as the competitive landscape.

β€’ Organize and facilitate both virtual and in-person onboarding and refresher training programs.

β€’ Collaborate across various functions, including Medical Affairs, Clinical Development, CMC, Regulatory, Quality, Commercial, and Patient Services.

β€’ Ensure that training documentation and certification processes align with FDA, EMA, and global compliance guidelines.

β€’ Create learning management systems and training analytics, incorporating key performance indicators for competency, certification, and launch readiness.

β€’ Work alongside HR to support company-wide onboarding initiatives for new employees.


⛳️ Requirements

β€’ An advanced degree is required (APN, PharmD, PhD, MD, or an equivalent qualification).

β€’ A minimum of 10 years of experience in the biotechnology or pharmaceutical sector.

β€’ At least 5 years in leadership roles within Medical Affairs or Medical Training.

β€’ Direct experience in cell therapy and/or gene therapy is highly preferred.

β€’ Preferred experience in neuroscience, neurology, and/or immunology.

β€’ Experience in supporting the launch of advanced therapies is strongly favored.

β€’ A solid understanding of regulatory and compliance frameworks related to advanced modalities.

β€’ Proven ability to establish infrastructure in clinical-stage or scaling biotech settings.

β€’ Exceptional communication skills, ability to foster cross-functional collaboration, and adeptness at managing complexity in fast-paced, resource-limited environments.


🏝️ Benefits

β€’ Eligibility for bonus incentives.

β€’ Comprehensive benefits package.

β€’ Participation in the company’s stock plan.

β€’ Approximately 15% travel required.

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