Clinical Research Associate

Posted 11 Hours Ago
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Kfar Saba
1-3 Years Experience
Healthtech • Software • Pharmaceutical
Join us as we drive change to combat serious chronic diseases.
The Role
Seeking a Clinical Research Associate with 2-3 years of experience in overseeing clinical trials and ensuring compliance with regulatory requirements. Responsibilities include overseeing clinical trials, developing relationships with stakeholders, reviewing adverse event cases, and conducting site visits. Bachelor's degree in Life Science or equivalent is required. IT proficiency and fluency in Hebrew and English are also necessary. Hybrid work model with office presence required three days a week.
Summary Generated by Built In

Are you passionate about clinical research? Do you have experience in overseeing clinical trials and ensuring compliance with regulatory requirements? We are looking for a Clinical Research Associate (CRA) to join our Clinical Development Center (CDC) at Novo Nordisk Israel. If you are ready for a challenging and rewarding career in clinical research, read on and apply today for a life-changing opportunity!
The Position
As a Clinical Research Associate at Novo Nordisk, you will:

  • Oversee the progress of clinical trials and ensure they are conducted, recorded, and reported in accordance with protocols, standard operating procedures (SOP), good clinical practices (GCP), and regulatory requirements.
  • Develop and maintain relationships with clinical investigators, medical educators, clinical research organizations (CRO), hospitals, and research institutions to initiate and expedite clinical studies.
  • Review adverse event cases with investigators, monitor timelines, prepare study documents, and issue status reports.
  • Plan and conduct Site Selection Visits (SSVs) as well as collect and archive site documents.
  • Prepare and conduct Site Initiation Visits (SIVs), as well as coordinate shipments to sites with required trial supplies.


Qualifications
To be successful in this role, we are looking for candidates with the following qualifications:

  • Bachelor's degree in a Life Science, Pharmacy, Nursing qualification or equivalent.
  • 2-3 years of experience in overseeing clinical trials and ensuring compliance with regulatory requirements.Knowledge of protocols, SOPs, GCP, and other applicable regulatory guidelines.
  • Strong communication and interpersonal skills to build and maintain relationships with stakeholders.
  • Good planning and organizational skills, project management skills, and proven excellence in the conduct of clinical trial activities from monitoring to the management of multinational trials.
  • IT proficiency: MS Office, clinical trials systems (e.g., COSMOS, IWRS, ePRO, NovoTime, CONNECT, HOT, Veeva)
  • Attention to detail and ability to work in a fast-paced environment.
  • Our offices located in Kfar Saba. This is a hybrid position which requires your presence in the office three days a week.
  • Fluency in Hebrew and English.


About The Department
The Clinical Development Center at Novo Nordisk Israel is responsible for running all clinical development activities, from initial planning of clinical trials to authority submission. Our team provides resources, processes, and competencies in biostatistics and programming, clinical reporting, data management, epidemiology/real-world evidence, and clinical pharmacology to support all development projects. We are committed to conducting high-quality clinical research and making a difference in the lives of patients.
Working at Novo Nordisk
We are a proud life-science company, and life is our reason to exist. We're inspired by life in all its forms and shapes, ups and downs, opportunities, and challenges. For employees at Novo Nordisk, life means many things - from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energise us to perform our best at work. Ultimately, life is why we're all here - to ensure that people can lead a life independent of chronic disease.
Deadline
12/07/2024
Contact
Please click on "Apply Now" and submit your resume in English.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we're life changing.

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What the Team is Saying

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Anders
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The Company
HQ: Bagsværd
64,000 Employees
Hybrid Workplace
Year Founded: 1923

What We Do

Novo Nordisk is a leading global healthcare company, founded in 1923 and headquartered in Denmark. Our purpose is to drive change to defeat diabetes and other serious chronic diseases such as obesity and rare blood and endocrine disorders. We do so by pioneering scientific breakthroughs, expanding access to our medicines, and working to prevent and ultimately cure disease.

We are powered by technology. Our Global Research Technologies, Medical Devices as a software, and Data Science teams are on the cutting edge of developing and supporting our life-saving medications.

Why Work With Us

Our purpose is to drive change to defeat serious chronic diseases, built upon our heritage in diabetes. We do so by pioneering scientific breakthroughs, expanding access to our medicines and working to prevent and ultimately cure the diseases we treat.

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Employees engage in a combination of remote and on-site work.

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