Name company: Association of Health, Food, Nutrition & Dietetics (AFND) www.afnd.in

Title: President

Experience abroad: No

Time period: from: 07.2011 I currently work here

Description: This association also targets to promote greater transparency and collaboration between individuals associated with the food industry and the study of nutrition that can best promote healthier lives through the right dietary practices. Though the association was started on the note to enlighten the community over the food, nutrition, and healthy lifestyle, the founders and researchers at AFND have understood that the factors that affect a healthy lifestyle are beyond just the food we eat. Thus, AFND now focuses on all the aspects of human and environmental health. We firmly believe that a sustainable environment is a key factor in altering human health. Our vision is to empower the interlinking of food, nutrition and dietetics that promotes optimal health for all To achieve the above vision, we Enhance awareness and the relevance of professions in the fields of Food, Nutrition, and Dietetics Engage professionals in an active learning-teaching environment, aspired by a close collaboration with members in other areas of expertise, with an ultimate focus on transforming lives through sound nutrition care Promote and safeguard the interests and goodwill of all its members.

Name company: Pepgra Healthcare Limited

Title: Director Of Business Operations

Experience abroad: No

Time period: from: 01.2017 I currently work here

Description: Devising and implementing the Clinical Operations strategy and plans. Contributes to relevant study documentation including clinical protocols, statistical analysis plan, clinical study reports as well as operational plan (CMP, DMP). Recruitment and management of the team. Negotiating the study budgets with the Principal Investigator and executing the Clinical Trial Agreement. Assigning and Managing the project team as per the study requirement. Monitoring the development and Revision of departmental SOPs. Oversee clinical trial sites adherence to pertinent regulations through review of monitoring reports, CQA-GCP audit reports, communication with investigators, study site personnel, CRAs, and other CRO/designee personnel. Reviews CRA Site Visit documents (follow up letters and reports). Reviews and Approves the travelling plan and budgets of the monitors. Updating the sponsor about the progress of the study as agreed in the contract. Participating in telecoms with the clients and kick of meetings. Hosting the external audits. Preparing Monitoring plan for the CRA as per the study specifications and protocol and training the CRA on the same. Training the team on study related documents. Involvements in bid proposals and leading bid defence.