Commercial Operations Sr Manager/ Associate Director, MLR & Meetings

Kyverna Therapeutics; United States; On-site; USD 175,000 - 205,000; Full time

Benefits offered by this job

Stock options

Bonus

Benefits

Job summary

Scorpion Therapeutics seeks a Senior Manager/Associate Director of Commercial Operations to support Kyverna's cell therapy platform. You will lead MLR processes, coordinate medical/legal/regulatory reviews, and manage commercial meetings with cross-functional teams.

Remote-friendly with West Coast hours preference, the role emphasizes compliance, process discipline, and strategic collaboration across marketing, medical, legal, regulatory, market access, and sales.

Qualifications

• Bachelor's degree required in a relevant field.
• 4+ years of experience in regulated industries (pharma/biotech/medical devices).
• Strong familiarity with MLR review, ideally in biotech or immunology.

Responsibilities

• Oversee end-to-end MLR review and cross-functional collaboration.
• Coordinate stakeholder input and manage asset lifecycle in Veeva PromoMats.
• Plan and execute conferences and internal/external meetings; improve workflows and KPIs.

Skills

Veeva PromoMats

Project management

Stakeholder coordination

Education

Bachelor's degree

Job description

Role

Senior Manager/Associate Director of Commercial Operations supporting Kyverna's cell therapy platform, primarily managing Medical, Legal, and Regulatory (MLR) review processes and commercial meetings.

Responsibilities

• oversee end-to-end MLR review, coordinate cross-functional stakeholder collaboration, manage Veeva PromoMats asset lifecycle, plan and execute conferences and internal/external meetings, and continuously improve operational workflows and KPIs.

Requirements

• bachelor’s degree; 4+ years experience in regulated industries like pharma, biotech, or medical devices, with strong familiarity with MLR review—preferably in biotech or immunology, especially related to autoimmune diseases.

Technical Skills

• hands-on Veeva PromoMats or similar platforms, project management, and stakeholder coordination.

Preferred

• experience supporting medical/legal/regulatory review, organizing commercial meetings, or biotech cell therapy programs.

High-Value

• remote role (West coast hours preferred), with emphasis on compliance, process discipline, and cross-functional collaboration across marketing, medical, legal, regulatory, market access, and sales teams.

Compensation

• $175K-$205K annually, plus bonus, benefits, and stock options.