
Clinical Research Coordinator
Welcome to Novo Nordisk, a global healthcare company dedicated to improving the lives of people with chronic diseases. We are currently seeking a highly motivated and detail-oriented Clinical Research Coordinator to join our team. In this role, you will play a vital role in the development and execution of clinical trials for new and existing treatments. This is an exciting opportunity for someone who is passionate about making a difference in the lives of patients and has a strong understanding of clinical research processes. If you have a background in life sciences and a desire to be a part of groundbreaking research, we encourage you to apply for this position. Join us and be a part of our mission to change diabetes and other serious chronic diseases.
- Spearhead the development and execution of clinical trials for new and existing treatments in accordance with company and regulatory guidelines.
- Oversee all aspects of clinical trials, including study design, protocol development, participant recruitment, and data collection and analysis.
- Collaborate with cross-functional teams to ensure smooth and efficient conduct of trials, including but not limited to medical affairs, regulatory affairs, and drug safety departments.
- Monitor and track progress of trials, ensuring adherence to timelines and budgets.
- Prepare and maintain all necessary documentation for trials, including study protocols, informed consent forms, and case report forms.
- Serve as a point of contact for study participants, addressing any concerns and providing necessary support and guidance.
- Maintain accurate and up-to-date records of all trial activities, including participant enrollment, adverse events, and data collection.
- Conduct site visits to ensure compliance with study protocols and regulatory requirements.
- Assist in the preparation of reports and presentations on trial results for internal and external stakeholders.
- Stay up-to-date on industry developments and best practices in clinical research to continuously improve trial processes and outcomes.
- Adhere to ethical standards and protect the rights and safety of study participants.
- Represent the company at scientific conferences and meetings to promote clinical research initiatives.
- Contribute to the overall mission of Novo Nordisk to improve the lives of people with chronic diseases, particularly diabetes.
- Foster a positive and collaborative work environment within the clinical research team.
Bachelor's Degree In A Related Field Such As Biology, Biochemistry, Or Healthcare.
Minimum Of 2 Years Of Experience In Clinical Research, Preferably In A Pharmaceutical Or Biotech Company.
Knowledge Of Good Clinical Practice (Gcp) Guidelines And Other Regulatory Requirements.
Strong Organizational And Project Management Skills.
Ability To Work Independently And As Part Of A Multidisciplinary Team.
Quality Assurance
Budget management
Medical Terminology
Data collection
Regulatory compliance
Clinical Trials
Patient Recruitment
Informed Consent
Protocol Management
Gcp (Good Clinical Practice)
Electronic Data
Communication
Conflict Resolution
Customer Service
Emotional Intelligence
Leadership
Problem Solving
Time management
creativity
Teamwork
Adaptability
According to JobzMall, the average salary range for a Clinical Research Coordinator in Princeton, NJ, USA is between $50,000 and $75,000 per year. Salaries may vary depending on factors such as education, experience, and specific job responsibilities.
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Novo Nordisk AS engages in the research, development, manufacture, and marketing of pharmaceutical products. It operates through the Diabetes and Obesity Care; and Biopharmaceuticals segments. The Diabetes and Obesity Care segment covers insulins, glucagon-like-peptide 1, other protein-related products, oral anti-diabetic drugs and obesity. The Biopharmaceuticals segment handles the research, development, manufacture, and distribution of products within the areas of haemophilia, growth hormone, hormone replacement, inflammation and other therapy areas.

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