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As a MEDICAL SCIENCE LIAISON in Algeria at Baxter you will play a pivotal role in advancing medical science and healthcare outcomes! This outstanding opportunity allows you to work with an elite team, providing invaluable contributions to clinical, scientific, and medical fields. You will be at the forefront of groundbreaking medical research, ensuring that our efforts are strictly aligned with the highest ethical standards and patient-centric principles.
Job Responsibility:
Identifies and advances clinical needs, ensuring that we continually meet the evolving requirements of the healthcare community
Acts as the primary contact for investigator-initiated trials, facilitating the successful implementation of research initiatives
Assists in the development of publication plans to share new findings and insights with the broader medical community
Supports the medical manager in the review of promotional materials, ensuring they compete with the highest standards of accuracy and compliance
Acts as a liaison with the medical community, including medical professional societies, leaders with a point of view, visionaries, investigators, and consultants
Supports the medical director/medical manager in collaborating with leaders with a point of view, encouraging relationships that drive innovation and excellence in medical science
Provides accurate and fair-balanced medical-scientific education and information on products, therapies, issues, trends, and clinical research
Conducts demonstrations and in-services at customer sites to ensure flawless clinical use of products
Assists in the development of medical-scientific advisory boards, symposia, and other educational forums
Educates and trains internal staff on products, therapies, issues, trends, and clinical research, ensuring our team remains at the forefront of medical knowledge
Provides scientific support to the sales team, empowering them with the insights needed to succeed
Supports the Medical Director or Manager in managing risks associated with field products and resolving clinical use issues
Ensures all risk management activities are completed with the highest degree of precision and efficacy
Ensures compliance of promotional materials with regulatory standards
Requirements:
Excellent product knowledge and expertise
Outstanding presentation and communications skills in both the local language and English
Proven teaching capabilities and an understanding of adult learning concepts
Effective critical thinking skills and strategy implementation
A broad understanding of the regulatory and healthcare environment in the country/region
Excellent organizational skills, resilience, and empathy
An MD and/or PhD and/or equivalent healthcare qualifications, preferably with proven MSL experience
2-3 years post-graduate experience within the healthcare industry
Clinical trial experience with knowledge of GCP
Training in adverse event reporting
Proficiency in computer literacy and Windows Office tools
Experience in literature review, analysis, and synthesis
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