US-NJ, Global Brand Medical Director - Oncology Medical Affairs 211384BR-MZ
Global Brand Medical Director - Oncology Medical Affairs
ONCOLOGY BU - NPH
East Hanover, NJ
Research & Development
Medical Affairs leader for assigned compound(s) and /or project(s under the leadership of a Sr. GBMD or GMA Franchise head. Responsible for the implementation of the strategy and execution of the Global Medical Affairs program(s) under the leadership of a Sr. GBMD or GMA Franchise Head.
For assigned compound/indications, work collaboratively across functions, within GPT to execute an integrated Medical Affairs plan including clinical trials, publication, medical education and medical information. Lead or co-leads GMA Strategic Sub teams within GPT, to gain strategic and planning alignment across regions and functions
Manages all operational aspects and drives execution for assigned projects of Global Medical Affairs clinical trials in partnership with global line functions, assigned Clinical Trial Heads (CTHs), and regional/country medical associates.
Participates and contributes to the joint ICT s.
Provides Medical leadership to CTT s for Novartis sponsored GMA trials
Leads review of investigator-sponsored trials and Local/Regional Medical Affairs trials concept sheets, within MRC, for assigned projects(s).
Supports medical training, medical education and commercial activities in alignment with the Global Brand Team. Provides medical support for educational events (e.g. stand-alone meetings, scientific symposia) and scientific congresses within legal and compliance regulations.
Collaborates across functions to achieve approval of key scientific communications, medical information documents and commercial documents within NP4 legal and compliance regulations.
Provides medical input on overall publication strategy and is a key member of publication planning team providing GMA medical input on individual publication plans.
Provides medical leadership in interactions with key external stakeholders e.g., leads advisory boards, under supervision of GMA Franchise Head or Sr. GBMD.
Responsible to efficiently manage budgets and resources for Novartis Sponsored and GMA supported activities, in collaboration with GMA Franchise Head or Sr. GBMD.
Key Performance Indicators:
Execution of Novartis-sponsored clinical trials and guidance of investigator-initiated trial programs.
Development of high-quality scientific communications and medical information.
Effective use of budget and resources in delivering high-quality Medical Affairs program.
Impact on the organization:
Timely implementation and delivery of high quality Medical affairs clinical programs within budget, in full compliance with Novartis Standard and GCP/ICH.
Well managed and effective clinical teams.
External satisfaction, acceptability of clinical data by key decision makers including health authorities, payers.
Strong alignment between Global and Regional/local organizations.
Strong alignment within Brand team and within GPT.
The Novartis Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status.
More than 4 years advanced knowledge in medical/scientific area (Oncology, Hematology, Endocrinology) preferred.
Fluent oral and written English.
1. Technical / Functional Skills
Have expert operational knowledge and experience in clinical trial design and all stages of clinical trial conduct (Trial design, Start-up, Execution, Analysis, Reporting).
Have an excellent knowledge of current clinical practice in Oncology / Hematology / Endocrinology or other relevant disease area.
Have strong knowledge in and understanding of medical activities (including scientific communications, medical information, MSLs, and HEOR), relating to the commercialization of oncology products.
Effectively engage external stakeholders across a broad range of audiences and activities.
3 years experience in pharma at local, regional and/or Global level.
2. Operational / Executional Skills
Can effectively manage and optimize resources and budget to meet business needs; have excellent project management skills.
Provide medical expertise to ensure successful product launches across functions.
Lead and manage different activities:
o NVS sponsored trials
o Review and coordinate IITs
o Implement patient access programs
o Review promotional materials
o Provide training to external and internal customers
o Define publication strategy and contribute to publication planning
o Review publications
3. People & Relationships
Build and lead high performing cross-functional teams collaboratively; effectively use rewards and recognition to create a culture of engagement and inclusion.
Acquire, develop, and retain exceptional talent.
Display a passion for building talent pipeline; provide feedback and coaching to team members on an ongoing basis.
Expertly lead and manage large, cross-functional, global teams to achieve high performance.
Build strong internal and external relationships with diverse stakeholders that maximize alignment and organizational effectiveness.
Can effectively manage different and diverse projects (clinical program, publication, medical education, Advisory boards)
4. Strategic Leadership
Effectively develop, communicate, and drive a long term vision and plan for medical affairs program, anticipating and addressing potential issues.
Display enterprise leadership in all aspects of the role by gaining alignment across functions and divisions.
Integrate medical expertise with commercial perspective.
Expertly manage ambiguity and highly complex situations.
Maintain an external focus to optimize and maximize treatment options and compound life cycle management.
Have excellent communications skills and ability to convey complex scientific and clinical concepts simply and effectively.
* If a direct employer requests that you go to their web site and complete your application there in order to be
considered, please do so. Applications for all positions are subject to each employer's specific requirements.