Clinical Research Professional
2 months ago
The Clinical Research Associate role at Novo Nordisk is a highly rewarding position for individuals driven by innovation and a desire to make a life-changing impact on patients.
About the Role
- As a Clinical Research Associate, you will be the primary point of contact between site staff and Novo Nordisk, acting as an ambassador for the company and contributing to making Novo Nordisk the preferred partner.
- You will be responsible for leading site management for the selection and initiation of sites, as well as conducting and closing activities of appointed studies in compliance with local regulations, ICH-GCP, Novo Nordisk procedures, and protocol requirements to ensure data quality and study subject protection.
- You will manage the site to meet patient recruitment rates and targets, delivering results that have a direct impact on the successful completion of the clinical program.
- You will coordinate with LTM and RTM teams, communicating progress and critical issues that may impair trial progress.
Requirements
- Bachelor's degree or above in Medical Science, e.g., medical, pharmacy, nursing, etc.
- Adequate English verbal and written skills
- Requires a minimum of one year of clinical trial experience within the pharmaceutical industry or CRO; preferably in clinical monitoring
- Knowledge of Good Clinical Practice (GCPs), ICH Guidelines, and local regulations, research process, and scientific knowledge as relates to clinical trial conduct.
- Willingness to travel
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