RELOCATION SUPPORT: This role is based in Mexico City, Mexico. Novartis is unable to offer relocation support: please only apply if accessible.
What if your expertise could help accelerate the development of life-changing medicines for patients around the world? As a Clinical Research Medical Advisor (CRMA), you will play a pivotal role in bringing innovative therapies closer to patients by shaping clinical trial strategy, driving operational excellence, and partnering with leading investigators and healthcare experts. This is a unique opportunity to combine scientific expertise with cross-functional leadership, influencing the successful delivery of clinical development programs while helping Novartis reimagine medicine for people everywhere.
Job Description
As a CRMA, you will provide Clinical Development and indication expertise specific to Country/Cluster, and together with the clinical trial operations team,
drives the execution of clinical trials with high quality and within planned timelines.
Key Responsibilities
Validates study designs, is accountable for, and makes the final decision on the clinical/medical trial and program feasibility of implementing a clinical trial protocol based on medical/clinical practice and analysis of the competitive environment in the country.
Actively contributes to scientific/clinical/medical aspects of the start-up phase to ensure fast clinical trial site start-up.
Provides clinical/medical expertise to clinical trial operations team members and clinical trial sites for Institutional Review Boards (IRB)/ Ethics Committee (EC) interactions.
Decides on site/Country-specific scientific/clinical/medical content of the Informed Consent Form (ICF) as needed and ensures appropriateness of patient suitable language.
Provides scientific/clinical/medical expertise during interactions with Country/Cluster external Experts (e.g., Regulatory
📌 Clinical Research Medical Advisor (Xico)
🏢 Healthcare Businesswomen’S Association
📍 Xico
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