Director, US Medical Promotional Review Cardiovascular

Cytokinetics is a specialty cardiovascular biopharmaceutical company, building on its over 25 years of pioneering scientific innovations in muscle biology, and advancing a pipeline of potential new medicines for patients suffering from diseases of cardiac muscle dysfunction.

The Director, US Promotional Medical Review, Cardiovascular (CV) plays a critical role in ensuring scientific integrity, medical accuracy, and appropriate communication of data across promotional and non-promotional materials in the US. Serving as a medical and scientific expert for assigned therapeutic areas and products, this individual will provide timely, rigorous review of materials in accordance with internal policies, established review standards, and applicable US laws, regulations, and regulatory guidance. Beyond formal review responsibilities, this role will serve as a solutions-oriented partner to Medical Affairs, Commercial, Regulatory, Legal, and Compliance colleagues, providing thoughtful medical guidance that enables clear, accurate, and scientifically balanced communications.

The role offers an opportunity to contribute to the evolution of review practices and governance, support cross-functional initiatives, and provide medical expertise to enable high-quality scientific and promotional communications.

Key Responsibilities:

• Maintain expert-level therapeutic area and product knowledge through ongoing assessment of relevant CV published literature, treatment guidelines, internal resources, and data

• Provide medical guidance in Medical, Legal, Regulatory (MLR) meetings and related initiatives, including medical and promotional review, disease/brand and launch planning, and key cross functional strategic initiatives

• Critically evaluate and offer strategically sound solutions for complex promotional and non- promotional tactics to ensure fair balance, medical and scientific accuracy, robust evidence support, appropriate statistical interpretation, and compliance with applicable regulations and guidance (eg, clinical guidelines, FDA/OPDP guidance)

• Review and evaluate evidence supporting promotional claims to ensure they are comprehensive, balanced, unbiased, scientifically rigorous, and statistically reliable, while advising stakeholders on appropriate scientific and clinical interpretation

• Proactively align and build strong relationships with Marketing, Market Access, Medical Affairs, Corporate Communications, Training, Legal, Regulatory Affairs, and Compliance to ensure consistent messaging and collaboration across stakeholders

• Participate in internal and external meetings (eg, training, education, medical congresses, and matrix team meetings) to stay current on regulations, medical/scientific developments, and Commercial and Medical strategy

• Develop and deliver ongoing training for internal cross-functional teams to ensure understanding of MLR standard operating procedures, policies, and standards requirements for approved data sources within materials

• Contribute to the development and continuous improvement of processes and standards for the development, review and approval of scientific materials and compliant data source requirements for materials for use with externally facing customers

• Apply digital and AI-enabled solutions to improve efficiency, consistency, and scalability of promotional review activities

• Stay informed of industry trends and promote best practice sharing across medical and promotional review teams

• Collaborate with medical communications vendors and agency partners to support review activities as needed

• Participate in periodic review of approved medical and promotional materials to ensure continued alignment with current evidence and labeling

• Contribute to content governance, process optimization, training and document lifecycle management

• The position title and level will be commensurate with the candidate’s experience and qualifications.

Qualifications:

• Advanced scientific degree (PharmD, PhD, or MD preferred)

• Minimum of 5-7 years of pharmaceutical/healthcare industry experience including direct experience in promotional MLR review; cardiovascular experience preferred

• Strong knowledge of clinical trial design and applied biostatistics, with the ability to critically interpret clinical data and assess the scientific validity of claims and data presentations

• Knowledge of the pharmaceutical industry and external compliance, transparency, and conflict-of- interest environments, including familiarity with FDA advertising and promotion regulations, OPDP enforcement trends, warning letters, and relevant FDA guidance documents

• Ability to interpret trial data and Real-World Evidence; significant experience with FDAMA 114 content and data consistent with FDA-approved labeling (CFL)

• Strong scientific/medical written and verbal communication skills

• Demonstrated ability to build strong cross-functional partnerships and influence stakeholders to achieve aligned outcomes

• Solution-oriented, highly accountable team player with the ability to thrive in a dynamic and evolving environment

• Experience leading cross-functional teams and stakeholders through change and navigating complex organizational dynamics

• Ability to travel 10% (domestically or internationally)

#LI-ONSITE

Pay Range:

The expected salary range for this position based on the primary location of South San Francisco, CA is $228,600-$266,700. The base pay offered will take into account internal equity and may vary depending on the candidate's geographic region, job-related knowledge, skills, and experience among other factors. Base salary is just one component of our competitive total compensation package, which includes equity in the form of stock options and/or restricted stock units, comprehensive health, dental, vision, life and disability insurance coverage, 401k retirement benefits with employer match, learning and wellness stipends, and paid time off. Note that benefits are subject to change and may vary based on jurisdiction of employment.

Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you.

Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.  

Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves.

Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers

Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process.

Here are some ways to check for authenticity:

• We do not conduct job interviews through non-standard text messaging applications

• We will never request personal information such as banking details until after an official offer has been accepted and verified

• We will never request that you purchase equipment or other items when interviewing or hiring

• If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com

Please visit our website at: www.cytokinetics.com

Cytokinetics is an Equal Opportunity Employer