DirecciónAbout the Role
Location: Mexico City, #LI-Hybrid
The position will be in charge of planning, execution, and interpretation of clinical trials research, data collection activities and clinical operations. May interact with investigational sites, clinical consultants, Contract Research Organizations & other vendors.
Key Responsibilities:
• Collaborates with Country medical/clinical colleagues, global clinical teams and directs activities to execute and deliver the assigned studies. Monitors patient data and study-related information related to clinical study sites and clinical trial participation.
• Ensures the investigator adheres to research protocols, regulatory requirements and good clinical practices and provides input into data validation plan. Provides timely and accurate monitoring of patient data and study-related information from source documents, research records, and site visits where applicable. May monitor study sites and audit facility selection.
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• Is a global clinical specialist overseeing all operational activities including planning, budgeting, implementing and completion of clinical trials in compliance with local and international regulatory requirements.
• Expert on monitoring processes, procedures, and systems. -Prepare and collect study site documents. -Perform Initiation Visit and continue to train study personnel as needed on study protocol, procedures, study drug handling and storage etc. -Perform Site Closeout activities per SOPs and applicable regulations.
• Is a seasoned, experienced professional with a full understanding of area of specialization; resolves a wide range of issues in creative ways. -Works on problems of diverse scope -Networks with senior internal and external personnel in own area of expertise. -Contributes to many cost center goals and objectives; may contribute to service line goals -May reviewand sign off Monitoring Visit Reports -Reporting of technical complaints.
Diversity & Inclusion / EEO
We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Role Requirements
Essential requirements:
• 3-5 years of Clinical Research Experience required
• Degree in scientific or healthcare discipline
• Languages: Fluent in both written and spoken Spanish and English language.
Why Novartis?
Our purpose is to reimagine medicine to improve and extend people's lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture
You'll receive: Competitive salary, annual bonus, flexible working arrangements, subsidized dining facilities, employee recognition scheme, professional development, learning experiences, diversity & inclusion.
Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here:
https://talentnetwork.novartis.com/network
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
Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network
Division
Development
Business Unit
GCO GDD
Location
Mexico
Site
Ciudad de México
Company / Legal Entity
NOV CORPORATIVO MEX
Functional Area
Research & Development
Job Type
Full Time
Employment Type
Regular
Shift Work
No
