Cytokinetics - Senior Medical Director, UK, Ireland & Nordics
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Requirements
• MD/MBBS with strong Medical Affairs experience. Cardiovascular experience preferred, clinical experience desirable. Position will be filled at a Director level (i.e. Director, or Senior Director) commensurate with experience. 7 years of pharmaceutical industry experience preferred. • Medical Affairs experience in the UK (with particular knowledge of the Countries market) with medicine approvals and peri-launch and launch activities. • Background in academic medicine, clinical research, and familiarity with study design, biostatistics and epidemiology desirable. • Proven ability to work independently and as a member of an integrated, interdisciplinary team in carrying out assigned responsibilities. • Must be analytical and articulate in both oral and writing skills, possess excellent presentation skills, with a demonstrated ability to communicate well with others at varying professional levels. • Familiarity with relevant regulatory authorization requirements and other key local authorities in the regional pharmaceutical industry. • Ability to think broadly about scientific communications and the impact on medical content. • Business fluent in English. Knowledge of other European languages are a plus. • Proficiency with Microsoft Office • Ability to travel within the UK, across Europe, and internationally (~35% of time) • 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 [email protected] • Please visit our website at: www.cytokinetics.com
Responsibilities
• Serves as an integral component of the Medical Affairs contribution to the UK launch of our late-stage cardiovascular clinical compounds, including: • Implementation of the Country Plan of Action based on the Global and European Medical Affairs Plan, • Execution of medical pre-launch and launch activities, • Education of Cardiovascular HCPs (heart failure and hypertrophic cardiomyopathy) regarding the clinical profile of our CV compounds and their place in therapy • Can speak to the mechanism of action of the compounds and their development, including Phase I-IV studies, at a detailed scientific level in a reactive conversation with key opinion leaders. • Provide day‐to‐day medical guidance while working closely on joint projects with other members of the Medical Affairs team, the Countries leadership, other departments internally and our business partners. • Projects may include scientific congress/conference strategy and planning, advisory boards, field force training, review of medical information standard response letters, health economics and epidemiology analyses, and marketing/policy related projects. • Represent the company at Medical Congresses and ensure Medical Affairs coverage, including scientific session attendance and reporting, and information booth support. • Represent the company in patient groups and associations. • Provide scientific input into publication strategy and review abstracts and posters for presentation at scientific meetings and manuscripts for publication. • Participate in appropriate cross‐functional and cross‐company Medical and Commercial teams in the UK to inform brand strategies and tactics and represent Medical Affairs. • Liaise with Global & European Medical Affairs and R&D colleagues to develop and maintain timely and relevant product expertise for the region. • Provide input into medical education, grant, and sponsorship review. • Provide clinical and scientific support in responding to inquiries from healthcare professionals. • Participate as medical reviewer in the Medical Review Committee and the Promotional Materials Review Committee • Data Generation and Presentation • Present data at company advisory board meetings and training programs • Collaborate with R&D and HEOR in data generation projects to address identified medical data gaps for the UK • Help identify and effectively interact with opinion leaders to engage in scientific exchange to meet the needs of patients and the medical community. • Collaborate with Market Access and the HEOR function to define research strategy and design of studies, including the generation of real-world evidence and cost-effectiveness analyses. • Provide support for and collaborate with the field medical teams in the UK and support reactive material development to address healthcare professional inquiries. • Upon initiation of a Phase 4 program, participate in the review and adjudication of investigator-sponsored study research proposals.
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