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#LI-Hybrid 12 days per month on-siteJob Description
Key responsibilities:
Leaddevelopment and execution of medical affairs strategy for Asset priority programs including transformative tactics such as research/population health innovative partnerships and integrated evidence plans.
Co-developplans for evidence generation MSL / Field Medical Affairs strategy medical education programs scientific publication planning and Medical Expert network development.
Co-ownthe development and implementation of innovative education and scientific communication plans for external stakeholders.
Trackfinancials to ensure timely and cost-effective development and execution of medical activities.
PrepareSRC submissions for TA assets within remit.
Partnerwith Development US and International cross-functional teams to shape the portfolio early and diversify evidence to achieve broad access at launch and enhance impact on clinical practice for priority programs.
RepresentGlobal Medical Affairs around prioritized portfolio with internal and external audiences in collaboration with TAs including the investment medical and regulatory communities as well as pharmaceutical or biotechnology industry collaborators/partners.
Advocatefor the voice of the patient internally and evaluate factors relevant to a patients informed decision-making.
Providedirection and input into the development and implementation of successful reimbursement and market-access strategies.
Contributeproactive input to Development on potential new therapeutic indications to enrich Registration Programs and explore new therapeutic opportunities.
Essential Requirements:
Fluent oral and written English.
PhD/PharmD in Health Sciences. Specialist Degree or specialist qualification related to discipline for which you will be responsible is an advantage.
Experience in Pharmaceutical Industry experience in Medical Affairs and/or Clinical Development.
Strategic mindset and able to establish credibility and influence across a range of diverse stakeholders in a matrix organization to drive change.
Deep understanding of health care systems and key external stakeholders.
Strong track record of delivery focus for time and quality in medical affairs projects.
Understands unmet medical needs generates the right evidence to fulfil them uses innovative multichannel communication formats for effective evidence dissemination.
Firm working knowledge of GCP scientific and clinical methodology protocol designs management and regulatory requirements for clinical studies designated for review by regulatory authorities.
Commitment to Diversity and Inclusion / EEO
Novartis is committed to building an outstanding inclusive work environment and diverse teams representative of the patients and communities we serve.
Skills Desired
Agility Agility Clinical Practices Cross-Functional Collaboration Data Analysis Drug Development Employee Development Healthcare Sector Understanding Health Sciences Influencing Skills Innovation Inspirational Leadership Integrated Evidence Generation Medical Affairs Medical Communication Medical Education Patient Care People Management Pharmaceutics Priority Disease Areas Expertise Product Launches Product Strategy Real World Evidence (RWE) Regulatory Compliance Research Methodologies 4 moreRequired Experience:
Exec
Full-Time