5!
This is the number of Therapeutic Areas that you can work with on a daily basis.
The Clinical Site Associate performs monitoring activities related to initiation, conduct (recruitment, quality data collection) and timely completion of clinical trials within the country.
The Clinical Site Associate is responsible for delivering data within timelines and required quality standards, and for adherence to monitoring procedures in accordance with GCP and ICH, local regulations, and SOPs.
Your responsibilities include, but are not limited to: Conducting feasibility and screening potential Investigators and networks to evaluate capabilities for conducting clinical trials.
Conducting site selection for potential sites to evaluate their capabilities for conducting a clinical trial and recommending sites to participate in clinical trials.
Being the front-line liaison between Novartis and sites to ensure successful collaboration, meeting Novartis expectations on milestones and deliveries.
Managing assigned study sites and networks, if applicable, conducting phase I-IV protocols according to the monitoring plan and Novartis procedures.
Performing Site Initiation Visits, ensuring site personnel are fully trained on all trial-related aspects and providing continuous training for amendments and new site personnel as required.
Collaborating with the CRA Group Head/CSM to ensure recruitment plans and execute contingency plans as needed.
Monitoring studies as per current legislation, ICH/GCP, and Novartis standards.
Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Minimum requirements: Degree in Scientific or Healthcare discipline.
Native Spanish, fluent English.
At least 2-3 years of experience in site monitoring.
Knowledge of international standards (GCP/ICH, FDA, EMEA).
Ability to travel domestically as needed to study sites and for training and meetings.
A minimum of 50% overnight travel may be required.
Advanced communication skills and team collaboration.
You'll receive: Competitive salary, annual bonus, pension scheme, health insurance, flexible working arrangements, subsidized dining facilities, employee recognition scheme.
Why consider Novartis?
769 million.
That's how many lives our products touched in 2020.
And while we're proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people's lives?
We believe the answers are found when curious, courageous, and collaborative people like you are brought together in an inspiring environment.
Where you're given opportunities to explore the power of digital and data.
Where you're empowered to risk failure by taking smart risks, and where you're surrounded by people who share your determination to tackle the world's toughest medical challenges.
Imagine what you could do at Novartis!
Division: Global Drug Development Business Unit: GDO GDD Country: Spain Work Location: Barcelona Company/Legal Entity: Novartis Farmacéutica, S.A. Functional Area: Research & Development Job Type: Full Time Employment Type: Regular Shift Work: No Early Talent: No #J-18808-Ljbffr