Clinical Research Coordinator

NovoBliss Research® Private Limited, based in Ahmedabad, India, is a leading CDSCO-registered and ISO 9001:2015 certified Contract Research Organization specializing in clinical safety and efficacy studies for Consumer HealthCare Products. With a focus on Nutraceuticals, Pharmaceuticals, Cosmetics, Dental, OTC, and Personal Healthcare products, NovoBliss is dedicated to delivering high-quality, ethically-driven research. As members of the Advertising Standards Council of India (ASCI) and the Indian Society for Clinical Research (ISCR), we uphold the highest standards of ethics and compliance. Founded by Dr. Nayan Patel and Dr. Maheshvari Patel, NovoBliss is committed to advancing global clinical research through scientific excellence, innovation, and integrity.

This is a full-time, on-site role for a Clinical Research Coordinator based in Ahmedabad. The Clinical Research Coordinator will be responsible for managing clinical trials, ensuring compliance with protocols, obtaining informed consent from participants, and coordinating research activities. The role also involves collaborating with investigators, maintaining study files, and ensuring adherence to regulatory requirements.

• Comprehensive knowledge and experience in Informed Consent processes and compliance with ethical standards.
• Proficiency in developing and managing study Protocols and ensuring their implementation during clinical trials.
• Strong background in Research with expertise in Clinical Research Experience and managing Clinical Trials.
• Excellent organizational and communication skills to effectively manage and support clinical trial operations.
• Bachelor’s degree in Life Sciences, Pharmacy, or a related field; advanced degrees are a plus.
• Good understanding of regulatory and ethical requirements associated with clinical research.
• Ability to manage multiple projects, timelines, and priorities in a collaborative team environment.