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Cytokinetics

Develops small-molecule therapies for muscle function

Director – Commercial Regulatory Europe

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeZug, SwitzerlandCHF200k - CHF250k /yrHybrid

About the Job

Requirements

  • At least 8 years of relevant experience, with expertise in applicable European regulations, directives, guidelines, and the EFPIA Code.
  • Prior experience in advertising and promotion regulatory roles.
  • Experience working with cross-functional teams across EU countries.
  • A solid understanding of clinical trial designs and results, and how non-clinical and clinical evidence can be used compliantly to substantiate promotional and non-promotional claims.
  • Experience with electronic approval systems; Veeva PromoMats experience is preferred.
  • Ability to communicate regulatory concepts effectively across functions.
  • Ability to work collaboratively and independently, including supporting and prioritizing multiple projects.
  • Ability to build and maintain professional networks.
  • Ability to identify challenges and problems and take initiative to identify solutions.

Responsibilities

  • Lead and manage the European MLR process, ensuring timely and compliant regulatory review of promotional and non-promotional materials in Europe.
  • Provide training and guidance to internal teams on regulatory requirements and best practices for promotional activities and other activities as required.
  • Develop and oversee local MLR activities through vendor selection and management, and serve as the primary liaison between the central regulatory affairs team and local regulatory vendors to align regulatory strategies and objectives.
  • Work with Commercial, Medical, Legal, and Compliance teams to ensure regulatory activities are conducted promptly and compliantly.
  • Ensure Advertising and Promotion activities comply with applicable regulations, guidelines, and Codes of Practice, maintaining up-to-date knowledge of regulatory requirements in each country’s jurisdiction.
  • Work cross-functionally to ensure relevant regional and local MLR standard operating procedures are in place.

Desired Qualifications

  • ABPI experience is an advantage.

About the Company

Cytokinetics

Develops small-molecule therapies for muscle function

Cytokinetics develops and commercializes small molecule drugs aimed at improving muscle function for cardiovascular and neuromuscular diseases. Its products are designed to either enhance or adjust muscle contraction, with a pipeline that includes compounds like omecamtiv mecarbil, reldesemtiv, CK-274, AMG 594, and CK-601, currently in various stages of clinical trials. The company advances therapies through partnerships, licensing, and potential sales of approved medicines, and relies on extensive clinical testing to demonstrate effectiveness and safety. What sets Cytokinetics apart is its focused approach on muscle function modulators (activators and inhibitors) for both heart and skeletal muscle diseases, targeting conditions such as heart failure, hypertrophic cardiomyopathy, ALS, and SMA. Its goal is to bring medicines to patients to improve muscle performance and daily function, addressing unmet medical needs in these diseases.

Company size
501-1,000
Company stage
IPO
Headquarters
South San Francisco, CA
Founded
1998

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