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., Re
📌 Clinical Research Medical Advisor (Xico)
🏢 Healthcare Businesswomen’S Association
📍 Xico
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