One of our clients, a well established hospital with branches in Bangalore, Mysuru, Mumbai and Delhi is looking for Fresher MBBS Doctor Qualifications and Experience Experience: Fresher Education: MBBS   Responsiblities Conduct regular thorough examinations on patients to check and record their health and normal physical development Examine sick patients to determine their condition and ask intuitive questions to gather information about symptoms Reach an informed diagnosis based on scientific knowledge and individual medical history Prescribe medications and give detailed instructions for administration Prescribe and interpret appropriate lab tests to gain more information about possible infections or abnormalities Prepare and administer vaccines according to the governmental vaccination plan Examine and treat injuries and refer the patients to physicians of other disciplines when necessary (e.g. surgeons, ophthalmologists, orthopedists etc.) Advise patients on diet, exercise and disease preventive measures Keep updated records of patients illnesses, surgeries or other medical episodes allergic shocks, injuries etc.

Responsibilities Caring for neonates at the remote NICUs from a centralized care center  Manage these patients and document their progress, troubleshoot ICU issues, coordinate bedside team in accordance with global standards, and escalate issues Should be aware of ICU patients monitoring parameters like SpO2, cardiorespiratory, NIBP, Invasive BP, CVP, ventilation parameters, non-invasive ventilation parameters, CPAP/HFNC settings and others Conducting tele rounds which involve patient review, daily rounds, review of labs and radiology, drug charts, compliance to protocols Liaising with the bedside team actively and providing critical care expertise in real time to augment the delivery of critical care to the NICUs Check-ins with regular intermittent tele rounds on sick patients and initiating appropriate actions with the help of the tele NICU team in collaboration with the bedside team Documenting patient-level data and communication in our smartICU platform, RADAR keeping records of their health in NICU, diagnosis and documenting patients' symptoms and medical history. Identifying changes in the infant?s symptoms and intervening in emergency situations Following appropriate guidelines and schedules Keeping and tracking records for vital signs like temperature, pulse, breathing, oxygenation and blood pressure, as well as any signs of distress due to birth asphyxia and trauma, respiratory distress, apnea, aspiration, sepsis, etc., in critically ill infants.   Qualification & Experience Fellowship in Neonatology or Pediatrics hands-on NICU experience in a well-reputed hospital  4 to 6 years of experience   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Responsibilities Drive launch preparation excellence in liaison with regions and affiliates and become therapeutic and brand experts while relying on deep technical expertise from CoEs. Initiate and develop target access profile, market access strategy and payer value story for the asset. Drive market access input for pipeline planning to support and impact key decision making fora in Novo Nordisk. Drive early strategic thinking on HTA & reimbursement strategy in liaison with regions and strategic markets and become therapeutic and brand expert. Independence and Decision Making. Innovation and Change.   Qualification & Experience An academic background in a relevant field (life sciences, economics, public health science, or similar) Minimum of 9 years of experience in value strategy, value communication or health economics and health outcomes research, ideally within pharmaceutical industry or consultancy. Advanced level competencies in: Healthcare policy and system insight.  

Responsibilities Recruit and Develop CRAs and implement necessary actions to improve their performance. Lead quality clinical trial projects (CDP and/or local) in the country. Provide trial related communication and insight to key internal and external stakeholders. Coordinate the clinical trial set-up in partnership with the COM. Maintain ongoing communication with Ethics Committees and the Health Authority, ensuring the Central and local (as applicable) Ethic Committee is provided with the documents requested.   Qualification & Experience 8 to 10 years of experience in managing global clinical trials as CRA/Sr. CRA (approx. 6 yrs) and Team lead/Trial Manager (aprox. 2 yrs) Currently leading/managing project team of CRAs and or CTAs Candidates with prior experience in handling Diabetes/Obesity/OSCD (Other Serious Chronic Diseases)/Hemophilia/Growth Hormone disorders trials will be preferred  

Responsibilities Subject Matter Expert for Lilly’s procedures, processes, tactic types, and support resources Understand Lilly’s culture, Medical Affairs and Marketing organizational structures, roles and responsibilities, including how both fit into the bigger picture of Medical Affairs / Marketing Services and Lilly organization Have a thorough understanding of Lilly’s quality requirements and processes (i.e., CIQ and MCA requirements) and must be capable of understanding and applying these requirements/processes when executing their role Model strong knowledge of medical and marketing tactic types and associated requirements medical and marketing tactic lifecycle external agency structures and processes systems, software, tools, and Supervisor resources the healthcare environment and regulated industry practices Awareness of Lilly’s disease states and products Actively lead and/or participate in deviation investigations Ensure Quality, Speed, Value, and Compliance throughout the Deliverable Review Lifecycle Follow organizational project management best practices Responsible/accountable for the oversight and delivery of assigned work Conduct capacity planning and resourcing Manage the agile needs of the changing portfolio Define, execute, and monitor CIQ/MCA guidelines and systems supporting LCCI LMS and US Medical Affairs teams for Identify continuous improvement of processes and quality systems, and implement process/procedure updates/changes Uphold Lilly procedures and processes Determine corrective actions to eliminate recurring issues and work with CIQ/MCA team in tracking and managing deviations Demonstrate ability to partner effectively with cross-functional colleagues and facilitate shared-learning forums to establish best practices and identify challenges across teams Measure and track process efficiency through defining metrics, analyzing data sources, and providing support for data-driven decisions by identifying patters and trends in data sets Coach, Manage, and Develop a Team Recruits, develops, and retains a strategic and operational top talent Builds an organizational culture aligned with Team Lilly – inclusion, innovation, acceleration, delivery, integrity, excellence, and respect for people. Utilize myPM process to operationalize organizational goals. Provides guidance, training and supervision to personnel including the following: Manages new-hire onboarding process for staff Develops and implements functional training Enables robust coaching process Utilizes Lilly coaching framework and partners with direct reports to create individual development planning/action planning Serves as a trusted career advisor by provide input on employee development and talent assessments. Works with HR to identify career opportunities and participate in succession planning activities. Monitors employee engagement and team health Provides technical support as needed Evaluates performance by conducting monitoring/audits. Ensures all direct reports are compliant with company policies, procedures, and regulations. Appropriately manage the workload of direct reports; monitors project timelines and quality; and ensures communication of priorities to direct reports.   Qualification & Experience 3 years’ experience as an editor, copyrighter, or proofreader medical and/or marketing, communications, advertising agency, or pharmaceutical industry. 2 years’ experience in formal management experience Proven experience leading/managing a strategic portfolio or business process. Ability to coach, collaborate, influence, network, and work effectively while leading others. Experience in project management.  

Responsibilities   Jointly develop the market/local KOL engagement plan with other MSLs, identify and segment KOLs according to their scientific interest and related affiliations and build the KOL network pre- and post-launch. Engage with KOLs using deep scientific expertise and knowledge of AZ's marketed products and compounds in development. Provide support to the Global Medicines Development (GMD) team on clinical site identification and patient recruitment for Phase I, II & III studies. Create opportunities to complement existing flow of clinical data for AZ's products in line with stakeholder needs, i.e., by identifying pre-clinical, clinical and post-marketing study investigators in alignment with the Development Plan, and engaging in discussions on the ISS Programme with potential investigators. Provides support to the internal Global Medicines Development (GMD) team on clinical site identification Engage with the medical / scientific community in a highly credible, balanced/objective way, representing AZ's dedication to and excellence in science Prepare and give relevant high level medical science presentations at congresses, symposia and scientific meetings Provide support for content development, agreeing agendas and delivery of effective clinical presentations e.g., advisory boards Help to develop medical science literature, i.e., write, edit and publish scientific articles and papers   Qualification & Experience MBBS/MD-Pharmacology Sound knowledge of basic research, drug discovery, drug development, clinical environment Experience in pharmaceutical industry, health care or research environment Proven ability to understand, assimilate and communicate scientific information Proven track record to engage and develop lasting relationships with key thought leaders in complex clinical environments  

Responsibilities Independently handle clinical regulatory writing activities across a complex portfolio of work. Author the most complex clinical-regulatory documents within a program by ensuring that relevant regulatory, technical and quality standards are achieved, and that relevant processes and best practice are applied. As part of a clinical delivery or submission team, provide strategic communications leadership to projects, establish communication standards and best practice, and continuously advocate for quality and efficiency. When acting as a submission lead, drive the development of the clinical Submission Communication Strategy (cSCS). Lead internal/external authoring teams and provide strong partnership with vendor medical writers to ensure delivery to time and quality. Drive the clinical interpretation of complex data and information and condense it into clear, concise and accurate messages that address customer information requirements. Be a strategic problem solver and demonstrate strategic review capabilities. Proactively collaborative with other functions at the program level. Support the development of Clinical Regulatory Writing Managers. Drive continuous improvement and operational excellence from a communications leadership perspective, including representing the skill on drug and non-drug projects, as required.   Qualification & Experience Life Sciences degree in an appropriate field. Significant medical writing experience in the pharmaceutical industry or CRO. Ability to advise and lead communication projects. Understand drug development and communication process from development, launch through life cycle management.  

Responsibilities As a Director, you will provide International CMC RA expertise across the business functions, lead key business improvement initiatives, and provide operational, tactical, and strategic International CMC RA expertise and direction for CMC submissions across the lifecycle of a product. You will also lead knowledge sharing and provide coaching both within CMC RA and wider business functions. Qualification  & Experience Degree /PhD or equivalent professional qualification in a science or technical field such as pharmacy, biology, chemistry or biological science. Breadth of knowledge of manufacturing, project, technical and regulatory project management. Strong understanding of regulatory affairs globally Direct Regulatory Affairs CMC experience with submissions for Synthetics and/or biologic and biotechnology derived products  

Responsibilities To ensure that the clinical study is conducted according to the approved protocol and applicable regulatory requirements. To protect rights, safety and welfare of subjects. Management of Investigational Products. To ensure that sufficient number of qualified medical, paramedical, and clerical staff is available to conduct the study. To ensure that all staff assisting in study is adequately trained on the protocol, investigational product and their duties. To be aware of regulatory requirements and acceptable standards for conduct of clinical trial and protection of human subjects. To ensure that the data is complete, accurate, legible and internally consistent and maintain timelines. To take all study related medical decisions. To ensure that adequate medical care is provided to the subject for any adverse event, including clinically significant laboratory values. In case of health related problems, the investigator should inform the subject's primary physician about the subject's participation in the trial, if the subject has a primary physician and if the subject agrees to the primary physician being informed. To Review AE / SAE reporting forms after it is filled by the physician / designee. To Provide timely inputs on the protocol To conduct study in compliance with protocol approved by IEC, sponsor and regulatory agencies whenever applicable. To document and explain any deviation from the approved protocol. To ensure initiation of study and proper conduct of study in compliance with the study protocol and GCP requirements and communicate with IEC about any deviation in the protocol.     Qualification & Experience MBBS OR MD 2 - 4 years of experience into Principal Investigator  

Responsibilities Thorough understanding of the global Clinical Evidence requirements for regulatory compliance in the European and Australian market. Understanding of Europe's new Medical Devices Regulation (MDR 2017/745) and the US FDA regulatory pathways for medical devices. Review analytical data from development studies and performance evaluation studies to ensure regulatory requirements are met. Completely review all existing documentation in support of meeting the applicable Essential Principles of the Regulation(s). Evaluate and identify gaps or deficiencies in documentation. Determine applicable testing requirements and standards for subject device. Review available clinical data, compile a comprehensive and compliant Clinical Evaluation Report (CER), and facilitate a Risk Assessment as necessary. Compile and/or review proposed labelling and Instructions for Use. Assess global regulatory requirements and make recommendations based specific regions to management to ensure technical documentation is compliant to introduce to global markets.   Qualification & Experience Tertiary qualifications such as an undergraduate science or engineering degree or equivalent. A minimum of 3+ years demonstrated success in the analysis and interpretation of regulatory documentation and technical writing. Thorough understanding of the requirements of the new European Medical Device Regulation (EU MDR) and some understanding of the Australian Medical Device Regulations. Extensive experience in Medical Writing and preparation of Clinical Evaluation Reports (CERs) Experience with preparing USA Premarket Notifications [510(k)s] (desirable) Excellent communication skills