Clinical Research Associate

CDC Estonia is part of Region South East Europe, Middle East and Africa (SEEMEA) and is a new set-up of clinical organization in Novo Nordisk Poland, covering a group of 16 countries including Bosnia and Herzegovina, Bulgaria, Croatia, Czech Republic, Estonia, Greece, Hungary, Latvia, Lithuania, North Macedonia, Italy, Romania, Serbia, Slovakia, Poland.

Are you a dedicated clinical trial professional with a direct site management experience? Are you highly motivated by being able to make a difference to improving patients’ lives? If yes, keep reading – this role might be just for you! 

As Clinical Research Associate, Site Management in the allocated clinical trials is your key responsibility. Your role is to select and initiate sites as well as, verify the accuracy and completeness of the trial data, conduct closing activities in compliance with local regulations. Ensure that the rights and well-being of human subjects are protected, and the conduct of the trial follows the current approved protocol, GCP and local legislations.

 Your main responsibilities will include:

• Training  and guiding the site staff in the protocol and trial procedures in compliance with all local and company requirements
• Acting as the main point of contact between trial sites and Novo Nordisk
• Building professional relationships with internal and external Key Stakeholders
• Ensuring compliant documentation flow
• Participating in audits and inspections at assigned sites and an affiliate

In order to be considered, you need to be fluent in both English and Estonian and have a valid driving licence.

To be successful in this role, we expect you to have:

• Master’s Degree in Life Science or similar disciplines
• 2-3 years of relevant experience in pharmaceutical company or CRO.
• IT proficiency: MS Office, clinical trials systems
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On a personal level, you should have the ability to lead without authority and have high focus on delivery and quality.  You have team oriented personality with high degree of flexibility and you cooperate easily even with difficult stakeholders thanks to your excellent communication and negotiation skills. You should have good decision-making and problem-solving capabilities and be strong in prioritizing task to meet tight deadlines. You are open to new challenges in a continuously developing environment.

Novo Nordisk is its people. We know that life is anything but linear and balancing what is important at different stages of our career is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 40,000 employees. Together, we go further. Together, we’re life changing.

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