Responsibilities Guides and represents the company in meetings with government officials in various ministries & departments in both central and states governments Ensures company's product line is reflected to best advantage and advocates activities are successfully pursued to shape the policy environment. Identifies business opportunities in states and works with the officials to facilitate reimbursement/inclusion of company therapies/products in state schemes Coordinate with various internal stake holders and identify/communicate new and appropriate business opportunities in government departments Develops stake holder map of key officials in central and state governments and ensures timely meetings with the said officials to advocate on company issues. Track competitive activities and new policies being deliberated in various departments of the central and state governments Monitor progress of legislative and other issues of interest to the company and provides analysis to company official. Directs and works with designated trade and business associations, advocacy groups on political, legislative and advocates on policy issues of importance to the company. Writes white papers on macro & micro issues impacting the company and country   Qualification & Experience A graduate/post-graduate 7-9 years of experience Computer literacy including sound knowledge of the MS Office suite of software Advanced proficiency with Microsoft Office especially Excel (Mandatory)  

Responsibilities Responding to patients medical problems; carrying out diagnosis, treatment and counselling wherever necessary; issuing prescriptions basis patient's medical history and medical diagnostics. Coordination with the Order Management Team Managing patient/customer/chemist queries regarding our products Documenting all necessary patient information like personal into, medical history, prior prescriptions etc. Maintaining confidentiality of patient information   Qualification & Experience MBBS/BAMS Degree Excellent communication and interpersonal skills Medical License in India is required Minimum 1-2 yrs experience is preferred   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Responsibilities Oversight of CRO / other vendors and study management- Oversees CRO pre-site selection and site initiation, interim close-out and co-monitoring visits to ensure compliance with protocol and regulatory requirements and to assure good site performance Assists in the management of CROs and other vendors to ensure project requirements are met Ensure proper overview and communicate to teams (including on-time or high quality) of monitoring activities, data flow, data validation Evaluating and monitoring the project progress and resources to ensure projects are on time and within budget Reviewing operational aspects of trial activity and clinical protocols, providing oversight for trial implementation activities User of systems and business technologies to document and track study and user progress Assist in review of clinical protocols, amendments, informed consents, CRF/source document design, protocol specific training documentation, administrative letters etc. Oversee TMF management and review TMF documents as necessary Perform regular reviews of data according to data review/monitoring guidelines (CTMS, EDC, IVRS etc.) Work with QA for CAPA documentation and resolution Assists in forecasting of IP requirement during the study and prepare IP requisition. Assists in preparing and obtaining approval for clinical trial budget and for any change in the budget during the study; annual forecasting and tracking of spend. Assist in overall project planning and execution for clinical protocols This position requires approximately 10% travel to domestic and international locations   Qualification & Experience Minimum 6 years clinical study management experience with at least 2 years direct multinational study management experience 2 + years dermatology experience Ability to manage delegated aspects of assigned clinical trials Ability to manage CROs and Clinical Study vendors Bachelor’s level degree in life sciences, pharmacy or nursing   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Responsibilities Providing client and family-centred therapy - to young children and families in individual and group settings, using evidence-based therapy modalities - both online and offline. Performing intakes and clinical assessments – interviewing families, child observation sessions, using various tools and reporting. Assessment methods are a crucial part of our treatment approaches at Children First. Delivering workshops and webinars - from ideation to execution. Proficiency in PPT and Excel is a must. Supervision - Internal training and external training opportunities for continued professional development. Participating in peer supervision models within the organisation to share and learn. We are looking for someone who shares our warm, authentic and child-centred approach to therapy.   Qualification & Experience Graduate / Postgraduate degrees in Occupational therapy Desirable: Certifications in sensory integration therapies/Oral placement therapies   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"    

Responsibilities Develop and implement strategies to drive medical excellence in trainings, quality assessment of medical records, and SOP creation. Collaborate with cross-functional teams to ensure compliance with regulatory requirements and industry standards. • Lead and mentor a team of medical professionals to achieve departmental goals and objectives. Oversee the development and implementation of medical education programs for healthcare professionals. Conduct regular audits and assessments of medical records to ensure quality and compliance. Develop and maintain SOPs related to medical excellence initiatives.     Qualification & Experience BVSc with at least 5 years’ experience MVSc with at least 3 years’ experience PhD   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Responsibilities The role involves diagnosing, treating, and managing patients with various medical conditions, documenting patient information, collaborating with other healthcare professionals, and staying up-to-date with medical advancements and research.   Qualification & Experience MD in Medicine Strong clinical skills and knowledge of medical practices and procedures Excellent communication and interpersonal skills Ability to work in a fast-paced and dynamic environment Good analytical and problem-solving skills Attention to detail and accuracy in documentation Experience working in a hospital or clinical setting is preferred   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Responsibilities Creating and writing trial protocols, and presenting these to the internal/external committee. Training site staff on therapeutic areas, protocol requirements, proper source documentation, and case report form completion. Ordering, tracking, and managing trial materials. Conducting regular site visits, coordinating project meetings, and writing visit reports. Implementing action plans for sites not meeting expectations. Liaising with regulatory authorities wherever required Ensuring compliance with internal SOPs and local regulations, and ICH and GCP guidelines. Other tasks and responsibilities as needed. Responsible for developing close relationship with key customers across India to understand clinical needs and proposed trail ideas Follow up with customer on a regular intervals during protocol development, execution, report generation and publication Ensures customer and all related staff understands final protocol and meets required timelines Ensures protocol is written as per global guidance and customers proposed plan Creates content for publication of report/article/clinical trial after data is fully analyzed and is ready for publication     Qualification & Experience Master’s degree in biological science or a related field. Min 6 plus years minimum experience in clinical research. Knowledge of the health care industry, terminology, and practices. Knowledge of India clinical trial regulations and their implementation.