The Medical Lead for Cardiovascular acts with the highest standards of integrity, provides scientific & medical leadership, in close collaboration with the Medical Director, to the local medical team and provides medical expertise to generate strategies, clinical data, analysis and communications that support the safe and effective use of our medicines in this therapeutic area.
Key Requirements and Competencies:
•Medical doctor (physician) highly experienced in cardiology is mandatory
•Designing and implementing clinical trials
•Developing and delivering presentations and publications in English and local language
•Exposure to compliance requirements and to pricing issues related to country
•Ability to work in cross-functional teams: the candidate should also be a strong team player should be able to work co-operatively with others in order to meet group and organizational goals, to consistently deliver on commitments and communicate opinions, facts and thoughts with transparency, honesty and clarity.
•Excellent oral and written communication skills are required
•Project management skills
•Strong compliance focus
•Medical Leadership in Spain and Portugal for Cardiovascular TA.
•Continuously update knowledge of products, patient treatment trends and scientific activities for Cardiovascular.
•Expert Contributor to Internal Customers (Marketing, Regulatory, OR, PV, Legal Counsel and Pricing & Reimbursement).
•Active member of extended medical and brand teams for designated products, Spain Brand team, Spain/EU Medical-Marketing Team
•Nominated Medical Signatory for Cardiovascular
•Driver of content and executor of Spain Medical strategy plans for cardiovascular
•Maintain direct contact with External Experts to gather insights and input on treatments, and gain a full understanding of patient needs and behaviors, as well as scientific activities
•Development and management of Medical tactical plans in close liaison with MSL Manager
•Expert clinical contributor to observational studies and clinical sections of health technology assessment reports
•Provide medical / product expertise to support clinical research activities locally and input in to European and global research strategy.
•To appropriately contribute to manage and support investigator-sponsored study proposals
•Develop local medical plans and contribute to brand plans and strategies.
•Contribute to development of educational programs, symposia, advisory boards and publications.
•Management of medical content for external peer-to-peer meetings.
•Management of thought leader interaction plans.