Jun 09, 2022

Job Description

250! The number of genomics research projects that are waiting for your data analysis expertise every year. Your work will be important towards faster discovery and development of next generation breakthrough therapies for unmet medical need.

Your key responsibilities:
Your responsibilities include, but not limited to:
• To provide clinical strategic and tactical leadership in the country to support GDD trials, clinical development plans which change the world, concept sheets/protocols and other clinical documents;
• To provide country clinical strategic guidance and feasibility assessment for NIBR PoC trials;
• Closely collaborates with the Trial Monitoring Organization and Medical Affairs to ensure successful allocation, fast clinical trial start up, recruitment according to planned timelines, early identification of potential delays and mitigation plan;
• May lead medical/clinical discussion with local regulatory interactions as needed (CTA, NDA meetings, label discussions, post-approval commitments etc.);
• Cooperates with local functions such as e.g. Medical Affairs, Patient access to identify and involve qualified investigators with recruitment potential and relevant key specialists for clinical development in order to exploit the value of the assigned project(s) in the context of the investigational product(s).

You’ll receive:
Competitive salary, annual bonus, flexible working arrangements, subsidized dining facilities, employee recognition scheme, professional development, learning experiences, diversity & inclusion.

Why consider Novartis?
766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives.

We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working.

We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying!

Imagine what you could do here at Novartis!

Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network

Diversity & Inclusion / EEO

Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Minimum Requirements

• Medical or Scientific Bachelor Degree as mandatory; It is a plus if you have a Master in Science; Sophisticated Spanish and English skills (written, reading and speaking);
• 5 years of validated experience in medical practice and fully trained in Drug Development including Clinical Research, GCP, local regulatory requirements has previous experience in Clinical Trials recruiting, identifying and advising researchers, identifying and evaluation Clinical Research Offices; ideally previous experience in Oncology Clinical Trials and move fast across different therapeutic areas ;
• Ability to lead a study from medical/clinical perspective and proven capability to problem seek; safety monitoring providing medical or scientific expertise in clinical trials; demonstrates a deep knowledge of how to adequately review and read a protocol to understand the design of clinical trial;
• Preferably working before in Pharma companies or with Pharma projects
Global Drug Development
Distrito Federal
Research & Development
Full Time
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Clinical Research Medical Advisor

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