
Clinical Research Coordinator
Hello and welcome! We are currently seeking a highly motivated and detail-oriented individual to join our team as a Clinical Research Coordinator at Novo Nordisk. As a global healthcare company, we are committed to improving the lives of people living with chronic diseases and are looking for someone who shares our passion and drive. In this role, you will play a crucial part in the development and execution of clinical trials, contributing to the advancement of innovative treatments. If you are a self-starter with excellent organizational skills and a strong background in clinical research, we invite you to apply for this exciting opportunity.
- Coordinate and oversee the execution of clinical trials within Novo Nordisk, ensuring adherence to all protocols and regulatory requirements.
- Collaborate with cross-functional teams, including physicians, scientists, and study sponsors, to develop and implement clinical trial plans.
- Facilitate the collection and analysis of data from clinical trials, ensuring accuracy and completeness.
- Manage study timelines and budgets, identifying and addressing any potential delays or issues that may arise.
- Communicate effectively with study participants and healthcare professionals to ensure proper understanding of study protocols and procedures.
- Maintain accurate and organized documentation of all study activities and results, in accordance with company and regulatory standards.
- Conduct site visits and monitor study progress to ensure compliance with regulations and protocols.
- Assist with the preparation and submission of regulatory documents for approval of clinical trials.
- Provide training and support to other team members and study site staff on study protocols and procedures.
- Stay up-to-date with industry developments and regulatory requirements related to clinical research, and implement changes as needed.
- Ensure the safety and well-being of study participants through proper protocol adherence and reporting of adverse events.
- Contribute to the development of new and improved processes and procedures to enhance the efficiency and quality of clinical trials.
- Represent Novo Nordisk in a professional and ethical manner at all times, promoting the company's mission and values.
Strong Knowledge Of Good Clinical Practice (Gcp) Guidelines And Regulatory Requirements For Clinical Trials.
Bachelor's Degree In A Relevant Field Such As Biology, Chemistry, Or Healthcare Administration.
At Least 2 Years Of Experience In A Clinical Research Setting, Preferably In The Pharmaceutical Industry.
Excellent Organizational And Time Management Skills, With The Ability To Effectively Manage Multiple Projects Simultaneously.
Experience With Electronic Data Capture Systems And Data Management Tools.
Budget management
Quality Control
Data collection
Regulatory compliance
Clinical monitoring
Patient Recruitment
Informed Consent
Protocol Management
Study Coordination
Adverse Event Reporting
Study Documentation
Communication
Conflict Resolution
Leadership
Time management
creativity
Organization
Critical thinking
Teamwork
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a Clinical Research Coordinator in Bengaluru, Karnataka, India is between ₹3,00,000-₹8,00,000 per year. This may vary depending on factors such as experience, qualifications, and the specific company or organization.
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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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