Novo Nordisk Clinical Research Jobs – Pharma Candidates Apply

Novo Nordisk Clinical Research Jobs – Pharma Candidates Apply

Novo Nordisk Pharma Job – Pharma Apply Online. Postgraduate and undergraduate pharma candidates apply. candidates are eligible to apply online for an Associate post. Associate analyst professional position that is available at Novo Nordisk, which is one of the world’s most successful pharmaceutical companies

Job Title: Clinical Research Associate for Clinical Development Centre

Qualifications

Below are the required skills.

• You hold a graduate degree in Medicine, Science, Pharmacy or other relevant degrees from a reputed institution. You have minimum experience of 2-4 years in Clinical Research.
• As a Clinical research professional, you should have solid experience in 1-2 multinational clinical trials phase 2-3 from site monitoring to initiation to site closure.
  You are required to be trained in ICH GCP guidelines and if applicable certification is also preferred.
• Strong strategic and analytical capabilities, with demonstrated experience in analysing complex situations
• A strong track record in thorough planning, execution and follow-up is required, with a creative and innovative attitude that will enable you to drive initiatives with operational excellence in mind

The position

As a CRA you will be responsible for the smooth conduct of all clinical trials sponsored by Novo Nordisk

India in accordance with good clinical research practice (GCP) guidelines by NN and inline local regulatory requirements.

• In this role you will act as an ambassador for the company, and you are a primary point of contact between site staff and Novo Nordisk.
• You will lead the site management activities for the selection (if applicable) and initiation of sites as well as conducting and closing activities of the appointed studies in compliance with local regulations, ICH- GCP, Novo Nordisk procedures and protocol requirements to ensure data quality and study subject protection. You are also responsible for recruitment at site levels.
• You will be responsible for efficient and accurate site selection visits, performing monitoring activities.
• Guide and train staff on safety information handling and systems to prevent deviations that may lead in comprising integrity and quality of trial conduct.

Apply Online

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