Clinical Research Associate (H852)

Clinical Research Associate (H852)

08 feb
Novartis Argentina S.A
Buenos Aires

08 feb

Novartis Argentina S.A

Buenos Aires

Job Description

250! The number of genomics research projects that are waiting for your data analysis expertise every year. Your work will be important towards faster discovery and development of next generation breakthrough therapies for unmet medical need.

Your key responsibilities:

Your responsibilities include, but not limited to:

•The Clinical Research Associate performs supervising activities related to initiation, conduct (recruitment, quality data collection) and timely completion in different Phases and for different Therapeutic Areas for Oncology and Pharma clinical trials within the country;

•The CRA is responsible to deliver data within timelines and required quality standard,

responsible for adherence to monitoring procedures in accordance internal and local regulations;

•Allocate, initiate and conduct of trials, conducts site selection and recommends potential sites to evaluate their abilities to conduct a clinical trial, performs site Closeout and ensures successful collaboration between the sites and Novartis to meet expectations on landmark and deliveries are met as planned; Identifies issues at sites; resolves issues and raise as appropriate and collaborates with internal partners;

•Performs continuous training for amendments and new site personnel and conducts continuous monitoring activities (onsite and remote) to ensure compliance with protocol, GCP, global and local regulations and processes to secure data integrity and patient safety;

•Documents supervising activities accurately following Novartis standards; Collaborates with the Clinical Research Associates Group Head/Clinical Study Manager to ensure recruitment plans and execute contingency plans, as needed; Performs additional task as assigned Delivery of quality data and compliance to quality standards;

•Participates from audit organization and inspection readiness activities for monitoring and site related activities as required and ensures implementation of corrective actions within specified timelines.

Minimum requirements

What you’ll bring to the role:

•Has a Life Science, Medical, Health or Scientific Degree or adequate equivalent; Sophisticated Spanish and English skills (written, reading and speaking);

•Has 2 years of validated experience in pharmaceutical development, clinical research, and/or supervising clinical trials' understanding of the international aspects of drug development process for different Therapeutic Areas and Phases; has the ability to work with different trials at the same time; budget and treatment management;

•Experience identifying new health institutes or CROs and work with the actual ones; build strong relation and arrangements with them;

•Preferably working before in Pharma companies or with Pharma projects; Must have knowledge on ICH-GCP, international (i.e. FDA, EMA) and local clinical trials regulations; Willing to travel;

•Has excellent abilities to communicate, influence, persuade and negotiate with different teams and partners; Has high ethic and integrity skills; Looks always for Operational Perfection; Has the ability to seek problems and sophisticated issues; Has excellent teammate skills.

You’ll receive:

Competitive salary, annual bonus, flexible working arrangements, subsidized dining facilities, employee recognition scheme, professional development, learning experiences, diversity & inclusion.

Why consider Novartis?

799 million. That’s how many lives our products touched in 2019. 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!

Commitment to Diversity & Inclusion:

Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential.

Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here:

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