Company Description NovoBliss Research®️ Private Limited is a leading CDSCO-registered and ISO 9001:2015 certified Contract Research Organization (CRO) located in Ahmedabad, Gujarat, India. Specializing in clinical validation of consumer healthcare products such as pharmaceuticals, cosmetics, OTC, nutraceuticals, cosmeceuticals, and Ayurvedic supplements, NovoBliss operates from a cutting-edge 12,000 sq. ft. facility. With over 40 years of combined experience, founders Dr. Nayan Patel and Dr. Maheshvari Patel, excel in dermatology, nutraceuticals, herbal medicine, and regulatory science. Renowned for regulatory acceptance, global credibility, and exceptional data analytics, NovoBliss supports clients in regulatory submissions, product claims substantiation, and evidence-based marketing. Role Description This is a full-time on-site role for an Experienced Medical Writer at NovoBliss Research®️ Private Limited, located in Ahmedabad. The Medical Writer will be responsible for producing scientific documents, managing medical communications, and conducting thorough research. Daily tasks include writing, editing, and ensuring the accuracy of clinical study reports, research articles, regulatory submissions, and marketing materials. The role requires collaboration with cross-functional teams to gather necessary information and meet project deadlines. Qualifications Scientific Writing, Medical Writing, and Writing skills Experience in Medical Communications and Research Proficiency in producing regulatory submissions and clinical study reports Excellent written and verbal communication skills Strong analytical and critical thinking abilities Ability to work independently and collaboratively with cross-functional teams Master's degree or higher in Life Sciences, Medicine, Pharmacy, or a related field Experience in the clinical research or healthcare industry is a plus Show more Show less

Company Description NovoBliss Research®, based in Ahmedabad, India, is a premier CDSCO registered and ISO 9001:2015 certified Contract Research Organization (CRO) specializing in clinical safety and efficacy studies for Consumer HealthCare Products. We conduct research across diverse sectors, including Nutraceuticals, Pharmaceuticals, Cosmetics, Dental, OTC, and Personal Healthcare products. As members of the Advertising Standards Council of India (ASCI) and the Indian Society for Clinical Research (ISCR), we uphold ethical research standards and regulatory compliance. Founded by Dr. Nayan Patel and Dr. Maheshvari Patel, we are dedicated to advancing global clinical research with a focus on scientific excellence, innovation, and integrity. Role Description This is a full-time, on-site role for an Experienced Clinical Research Coordinator located in Ahmedabad. The Clinical Research Coordinator will be responsible for ensuring the smooth and efficient day-to-day operations of clinical trials. Tasks include obtaining informed consent, adhering to research protocols, managing study participants, coordinating with clinical staff, collecting and analyzing data, and ensuring regulatory compliance. Qualifications BA/BE experience is plus - minimum 2-3 years Experience with Informed Consent and Protocol adherence Proven Clinical Research Experience, especially in managing Clinical Trials Strong Research skills and ability to work with diverse healthcare products Excellent communication and organizational skills Bachelor’s degree in a relevant field or equivalent experience Commitment to maintaining high ethical standards and regulatory compliance Detail-oriented with strong documentation skills Ability to work effectively in a team environment Previous experience in a Contract Research Organization (CRO) or similar setting is a plus