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Director of Clinical Affairs

Location: Los Angeles. The job can be performed on a hybrid basis.

 

Company Overview:

Rubato is a startup company revolutionizing care delivery through our AI-powered music therapy platform. Our cutting-edge technology goes beyond traditional methods by harnessing the power of artificial intelligence to create personalized therapeutic experiences that enhance patient well-being.

By utilizing real-time biomarkers and data-driven music therapy, we deliver precision digital therapeutics tailored to each individual's physiological and emotional needs. Seamlessly integrating into existing care protocols, Rubato not only reduces patient behaviors and anxiety but also boosts engagement and adherence to care plans. Join us on the frontier of healthcare innovation and be part of a music therapy future, where technology and compassionate care converge.

 

Position Overview:

We are looking for a knowledgeable and experienced Director of Clinical Affairs to lead our clinical strategy and ensure the successful development and implementation of our AI-based Music intervention. This role will involve overseeing clinical trials, regulatory submissions, Data collection, and collaborations with key opinion leaders and healthcare professionals.

 

Key Responsibilities:

  • Develop and implement the clinical strategy for the product portfolio, aligned with the company's mission and regulatory requirements.

  • Design, oversee, and manage clinical trials, ensuring adherence to protocols, timelines, and budget.

  • Collaborate with internal teams to ensure product development is informed by clinical insights and evidence-based research.

  • Prepare and submit regulatory documents to appropriate agencies, ensuring compliance with all legal and ethical standards.

  • Establish and maintain relationships with key opinion leaders, clinical advisors, and healthcare partners to drive clinical validation and adoption.

  • Analyze clinical data, monitor study progress, and report findings to stakeholders, making recommendations for product enhancements.

  • Stay abreast of industry trends, advancements in digital therapeutics, and regulatory changes impacting clinical affairs.

 

 

Qualifications:

  • 5+ years of experience in clinical affairs, clinical research, or related roles, with at least 3 years in a leadership capacity.

  • Strong understanding of digital health and therapeutics, along with knowledge of regulatory frameworks (e.g., FDA, EMA).

  • Proven track record of successfully managing clinical trials from inception to completion.

  • Excellent communication and interpersonal skills, with the ability to engage with diverse stakeholders.

  • Strategic thinker with strong problem-solving abilities and attention to detail.

  • Advanced degree in a relevant field (e.g., PhD, PharmD).  

  • Medical degree (MD or DO) - Advantage.

 

What We Offer:

Competitive salary and equity options.

Comprehensive health and wellness benefits.

A flexible work environment with opportunities for professional development.

The chance to contribute to meaningful health solutions that improve patient lives.

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