Cytokinetics Inc jobs

Therapeutic Medical Scientist, Italy Milan, Italy Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility. Therapeutic Medical Scientist (Medical Science Liaison) Reporting to the Senior Medical Director for Italy, the TMS is a scientific professional who serves as a key field-based scientific resource for healthcare providers, patients, industry partners and internal colleagues. This role will come with high visibility in our company including critical cross-functional relationships across Medical Affairs, Clinical Development / Operations, and Commercial. This role will focus on key opinion leaders and other HCP's in the hypertrophic cardiomyopathy therapeutic area, but also support pipeline products in development. Our passion is anchored in rigorous and diligent scientific and clinical approaches to the discovery and development of novel mechanism therapeutics. With gratitude for the commitments and convictions of our employees who are inspired by the courage of patients we aim to serve, we believe Cytokinetics will continue to be a pioneering, values-driven, sustainable, fully integrated biopharmaceutical company. Role and Responsibilities: Identify national, regional, and local Key Opinion Leaders (KOLs) involved in the provision of cardiovascular care within institutional care centres and engage them in proactive and reactive scientific exchange Maintain and enhance existing scientific collaboration and

Associate Scientist South San Francisco, California posted: Posted 2 Days Ago

Senior Research Associate South San Francisco, California posted: Posted 30+ Days Ago

Head of Investor Relations South San Francisco, California posted: Posted 22 Days Ago

Senior Medical Science Liaison UK posted: Posted 28 Days Ago

Associate Medical Director, Spain Spain posted: Posted 30+ Days Ago

Associate Director, Medical Science Liaison (MSL) - West Virginia, Virginia, Maryland, and Washington, DC 4 Locations posted: Posted 30+ Days Ago

Contractor – Sr. Quality Associate Dublin, Dublin, Ireland Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility. Job purpose The role will provide structured assistance across document management, complaints handling, reporting, and general administrative activities. Securing this support will improve operational efficiency, strengthen compliance, and enable QA professionals to focus on high-value quality and oversight responsibilities. The Quality Department operates in a highly regulated environment with increasing demands related to documentation, customer assurance, and quality reporting. QA administrative workload has grown significantly, particularly in areas such as complaints management, CMO scorecard development, and compliance checks. Responsibilities The Quality Associate support will initially provide approximately 20 hours per week of support across the following key areas Document Creation and Execution Support Preparation, formatting, and maintenance of QA documentation within Veeva Coordination of document lifecycle activities including review and version control Ensuring adherence to internal documentation standards Complaints Management Support Initiating and tracking of customer complaints Supporting data entry, documentation, and follow-up activities Assisting in maintaining audit-ready complaint records CMO Scorecard Development Supporting data collection and consolidation for CMO performance metrics Assisting in the preparation and formatting of scorecards and reports Maintaining consistency and accuracy in reporting outputs

Director, Regulatory Affairs South San Francisco, California posted: Posted 2 Days Ago

Contract – Senior Research Associate South San Francisco, California posted: Posted 17 Days Ago

Contract Clinical Systems Specialist Remote posted: Posted 30+ Days Ago

Director, Regulatory Affairs, Europe (contractor) Zug, Switzerland Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility. Cytokinetics is dedicated to upholding the highest standards of excellence to bring potential medicines to patients to improve outcomes and quality of life. We are looking for Regulatory Affairs professionals who bring a strategic mindset and a deep understanding of the regulatory environment. As a member of the team, you will play a crucial role in ensuring our processes meet regulatory requirements while maintaining high standards of compliance. Cytokinetics is seeking an experienced Director, Regulatory Affairs Europe to join the Regulatory Affairs team in Europe. He/she will provide leadership in developing and executing best in class regulatory strategies for assigned programs in the European region. The Director will lead regulatory activities related to the submission of Marketing Authorization Applications of assigned Cytokinetics products in Europe as well as implementation of post-marketing requirements. The Director, Regulatory Affairs Europe will work closely with the Global Regulatory Lead and be a member of the Global Regulatory Team. He/she will work cross-functionally including with Clinical Research, Medical Affairs, Drug Safety, Quality, Market Access and with country operations to ensure all regional and local regulatory

Senior Manager, Quality Compliance South San Francisco, California posted: Posted 14 Days Ago

Senior Manager, Regulatory Writing Remote posted: Posted 22 Days Ago

Senior Manager, Supply Chain & Technical Project Management Dublin, Dublin, Ireland Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility. We are currently seeking a Senior Manager, Supply Chain and Technical Project Management in our Global Supply Chain & Technical Operations department. This position is integral to the advancement of Cytokinetics' growing portfolio of drug candidates and technology programs and will coordinate cross-functionally to ensure project deliverables are met on-time, on-budget, and with a high degree of quality. Reporting to the Director of Portfolio Management within Global Supply Chain & Technical Operations, this role will be responsible for the creation, and management of timelines, and deliverables to support the technical development, validation, and commercialization of drug substances, formulated drug product and packaging using Cytokinetics internal resources and an external network of providers. Responsibilities Provide project management support at any stage of the drug development lifecycle (e.g., early to late-stage development, market authorization, or post-launch phases) Develop charters, integrated schedules, deliverable lists, status updates, resource requests and related communications for assigned projects and programs Maintain a positive, results-oriented work environment by building partnerships, modeling collaboration and communicating in an open, balanced and objective manner to enable a

Associate Director, New Product Introduction Ireland posted: Posted 28 Days Ago

Director, Market Access Italy Italy posted: Posted 21 Days Ago

Associate Director, Commercial Analytics 2 Locations posted: Posted 30+ Days Ago

Medical Science Liaison (TMS) Paris, Paris, France Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility. At Cytokinetics, each team member plays an integral part in advancing our mission to improve the lives of patients. We are seeking tenacious, compassionate, and collaborative individuals who are driven to make a positive impact. The Medical Scientist will work as a member of the Medical team to support Cytokinetics portfolio with products in different phases of lifecycle and relay field-based clinical/medical insights back to Cytokinetics to impact the future strategy so Cytokinetics can continue to bring innovative medicines to patients with cardiac diseases. Reporting to the Associate Medical Director and in close cross-functional alignment, the Medical Scientist is a scientific professional who serves as a key field-based scientific resource for healthcare providers, patients, industry partners and internal colleagues. This role will come with high visibility in our company with critical cross-functional relationships across Medical Affairs, Clinical Development / Operations, and Commercial. This role will focus on key opinion leaders and other HCPs in the cardiovascular space and especially in the hypertrophic cardiomyopathy therapeutic area, but also support pipeline products in development. Our passion is anchored in rigorous and diligent

Executive Assistant, Global Supply Chain & Technical Operations Radnor, Pennsylvania posted: Posted Yesterday

Director, Access and Experience Marketing 2 Locations posted: Posted 30+ Days Ago

Head of Clinical Pharmacology South San Francisco, California posted: Posted 22 Days Ago

Key Account and Access Manager UK Remote - UK posted: Posted 30+ Days Ago

Senior HCP Marketing Manager Radnor, Pennsylvania posted: Posted 14 Days Ago