Novartis recruiting Head Medical Affairs West Africa
Head, Medical Affairs West Africa / SSA Medical GovernanceNovartis - Lagos |
Medical Affairs Strategy and Operations
- Define the Country (Group) Medical Affairs strategy and plan, including data generation, communication and Medical Expert engagement plans, ensuring strategic alignment with Cluster/Region
- Drive and lead clinical trials planning and execution within Country (Group)
- Ensures appropriate dissemination of trial-generated medical information to educate medical, scientific and regulatory leaders
- Is part of the development of the overall long-term strategy for the Country (Group): portfolio, growth, business partnerships, ‘roadmap’ for medical and regulatory activities
- Ensures adherence to financial and headcount targets for MA in the Country (Group)
- Acts as sponsor and contributor to relevant local and Global business/Franchise initiatives Regulatory, Safety and Risk Management
- Is accountable for adherence to all relevant safety standards, regulations and current legislation Internal / External Relationships
- Manages country interface with Global/Region/Cluster Clinical Development/ Medical Affairs, taking accountability for and optimizing all in-country clinical trials, scientific communication activities and engagement plans and drives their ultimate success
- Represents the country medical and scientific interests in internal and external (incl. HQ) activities Talent Development
- Maintains and drives the standards of medical and scientific excellence in the country through recruitment, training, deployment and development
- Support Country (Group) medical departments and MSL functions with medical capabilities and through capability building, as appropriate
- Provide medical leadership and strategic advice to Country (Group) medical departments, guiding them Above Country (Group) Activities:
- Drives key activities related to medical operations (e.g. data generation, capability building, launch readiness etc) or medical governance (e.g. GxP excellence, financial/operational controls etc) within/across country groups or cluster
Minimum requirements
Education: MD (or PhD if local requirements permit)
Language: English and local language/s: fluent spoken and written
Experience:
1. More than 5 years’ experience in clinical medicine and/or research
2. Knowledge of assigned therapeutic area with ability to interact with relevant KOLs.
3. Medical and scientific writing skills.
4. Familiar with all aspects of drug development, GCP and local regulations
5. Knowledge of clinical trial design, statistics.
6. Familiar with marketing principles and strategies.
7. Excellent interpersonal, communication, negotiation, and presentation skills.
Language: English and local language/s: fluent spoken and written
Experience:
1. More than 5 years’ experience in clinical medicine and/or research
2. Knowledge of assigned therapeutic area with ability to interact with relevant KOLs.
3. Medical and scientific writing skills.
4. Familiar with all aspects of drug development, GCP and local regulations
5. Knowledge of clinical trial design, statistics.
6. Familiar with marketing principles and strategies.
7. Excellent interpersonal, communication, negotiation, and presentation skills.
Division
PHARMA
Business Unit
AMAC
Country
Nigeria
Work Location
Lagos
Company/Legal Entity
Novartis Nigeria
Functional Area
Research & Development
Job Type
Full Time
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