Clinical Research Medical Advisor
Novartis · Insurgentes, Mexico · full time · On site · September 23, 2026
Why a CV for this job?
- They see what they asked for, first. Your experience that matches the ad leads, in the ad's own words, so someone skimming finds it in seconds.
- It gets past the software. Many larger employers use software that ranks CVs by how closely they match the ad, often before anyone reads them.
- In the language of the ad. An ad written in Spanish gets a CV in Spanish, even when yours is in Portuguese.
- Your facts, nothing invented. Your own experience, reordered and reworded. What the ad wants and your CV does not show is listed for you to add, only if it is true. You check it before you send it.
Job Description Summary
WORK ARRANGEMENT: Hybrid Working, #LI-Hybrid
LOCATION: Mexico City, Mexico
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.
Why Novartis:
Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
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 Authorities, Medical Experts, Advisory Boards, Patient Advocacy Groups, etc.).
- Drives patient recruitment strategies and proactively address enrolment and data quality challenges.
- Collaborate across functions to deliver high-quality clinical trials on schedule and in compliance.
Essential Requirements
- Advanced scientific degree in Medicine, Pharmacy, or Life Sciences and ideally, 3 years of clinical development experience in the pharmaceutical industry or clinical practice
- Ability to manage a study from a scientific/medical/clinical perspective, and a demonstrated capability to problem solve and mediate complex scientific/clinical/medical/operational issues.
- Ability to lead effectively by communicating well, motivating a cross functional team, and handling and delegating responsibilities.
- Ability to evaluate protocol feasibility and solve complex clinical challenges.
- Sound understanding of the overall clinical development process, and International Conference on Harmonization (ICH)/ Good Clinical Practice (GCP) principles
- Excellent communication skills with experience influencing cross-functional stakeholders. Fluency in Spanish & English are essential.
- Demonstrate an agile mindset by setting clear priorities, collaborating openly, and using feedback to make step-by-step improvements
Skills Desired
Clinical Research, Clinical Trials, Drug Development, Health Sciences, Regulatory Compliance
Benefits and Rewards:
Learn about all the ways we’ll help you thrive personally and professionally.
Read our handbook (PDF 30 MB)
Commitment to Diversity and Inclusion:
Novartis is committed to building an outstanding, inclusive work environment and diverse team representative of the patients and communities we serve.
Band
Level 4
Accessibility and accommodation:
Novartis is committed to work with and provide reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to tas.mexico@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
- Employer
- Novartis
- Location
- Insurgentes, Mexico · On site
- Contract
- full time