Clinical Research Associate
4 weeks ago
Are you passionate about driving innovation in clinical research? Do you have a strong background in site management and a keen eye for detail? We're seeking a Clinical Research Associate to join our team at Novo Nordisk. In this role, you'll be responsible for leading site management activities, ensuring compliance with local regulations and ICH-GCP guidelines, and delivering high-quality results that impact the success of our clinical programs.
Key Responsibilities:
- Lead site management activities, including site selection, initiation, and conduct of clinical trials
- Ensure compliance with local regulations, ICH-GCP guidelines, and Novo Nordisk procedures
- Deliver high-quality results that impact the success of our clinical programs
- Collaborate with cross-functional teams to ensure seamless trial execution
Requirements:
- Bachelor's degree or above in a relevant field (e.g. medical science, pharmacy, nursing)
- Adequate English verbal and written skills
- Minimum of one year clinical trial experience within the pharmaceutical industry or CRO
- Knowledge of Good Clinical Practice (GCPs), ICH Guidelines, and local regulations
About the Department:
In CMRQ, we're committed to bringing our products to market with speed and quality, and communicating their benefits to our customers in a scientific and effective way. We're a team of 6, working together to evaluate portfolios, approve new products, and conduct clinical trials.
Working at Novo Nordisk:
We're committed to creating an inclusive culture that celebrates diversity and promotes equality of opportunity for all our employees, patients, and communities. We're happy to discuss flexible working arrangements, depending on the role and business needs.
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