REQ-10034492
des 20, 2024
Mexico

Sammendrag

-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 & study-related information from source documents, research records, and site visits where applicable. May monitor study sites and audit facility selection.

About the Role

Major accountabilities:

  • Assist the clinical research team in preparing safety reports document for Investiga -Normally receives detailed instructions on all work -Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable)

Key performance indicators:

  • Deliver customer satisfaction results for internal and external customers -Delivery of Clinical Trials to quality standards and agreed timelines -Adherence to Novartis policy and guidelines and external regulations

Minimum Requirements:
Work Experience:

  • Fix-its/Turnarounds.
  • Project Management.
  • Operations Management and Execution.
  • Collaborating across boundaries.

Skills:

  • Clinical Monitoring.
  • Clinical Research.
  • Clinical Study Reports.
  • Clinical Trials.
  • Databases.
  • Problem Solving Skills.

Languages :

  • English.

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

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Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards

Development
Innovative Medicines
Mexico
INSURGENTES
Research & Development
Full time
Regular
No

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 [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

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

A female Novartis scientist wearing a white lab coat and glasses, smiles in front of laboratory equipment.
REQ-10034492

Study Start-Up Clinical Research Associate

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