Responsibilities The candidate will be responsible for drafting scientific protocols, executing, and presenting reports on real-world data queries raised by our pharmaceutical partners OR internal members. They will execute real-world queries by programming comprehensively from start to finish. The required coding skills include advanced proficiency in dataframe manipulation, the ability to run deep-learning models, parse model outputs, and generate summaries. The candidate will provide clinical insights to address questions from both internal members and external customers. Furthermore, the candidate will contribute to the development of technical products within the company by offering a detailed end-user perspective. They will lead a team, guiding their work and ensuring that the team remains motivated. The tasks conducted by the team are diverse, ranging from tagging datasets and harmonizing clinical entities to conducting chart reviews to identify pertinent information or generating metrics for the performance of AI/ML models. The candidate should have the capability to lead and contribute to the development of research works that are publishable in indexed journals, news articles, blogs, or marketing materials.   Qualification & Experience An MBBS or MD degree from a prestigious institution, either within India or internationally. A postgraduate degree is preferred, though candidates with exceptional backgrounds holding only an MBBS degree may also be considered. Proficiency in at least one programming language, preferably Python or R, with the capability to independently tackle data science problems. A proven track record of working towards specific goals in the past. Previous failures do not disqualify; the key is demonstrating a commitment to goal-oriented efforts. Candidates should have either 4 to 6 years of experience post-graduation or 8 to 10 years of experience after obtaining their MBBS degree, specifically within the med-tech sector or a related field. During this period, the candidate must have occupied a lead or managerial role for at least 25% of their time.  

Responsibilities Recruit, onboard, train and manage talent for building organizational capabilities. Manage deliverables (protocols, reports, literature searches, succinctly summarizing scientific content) and metrics with efficient planning, scheduling and resource allocations. Author clinical trial protocols, interim and final clinical study reports, integrated safety/performance data summaries from raw data as applicable. Perform formal literature searches, and succinctly summarize scientific content for assigned projects. Interprets literature information and synthesizes the information in clinical regulatory documents. Provide clinical science subject matter expertise and consultation to clinical research associates, biostatistics, data management, regulatory affairs, medical Safety and other internal and external stakeholders. Compiles clinical evidence from multiple sources such as current and past clinical trials, post market clinical follow up data and literature review updates, ad-hoc analysis, meta analyses, or other sources of safety and performance data (e.g. IIS clinical data, as available) and synthesizes the information in support of EU- MDR submissions, required CERs, and annual updates.     Qualification & Experience A minimum of a bachelor’s degree (BA or BS) in a technical and/or scientific discipline required. Master’s or Ph.D. or other higher degree in health-related field (RN, BSN, BPharm/MD/MPH) is required 8+ years of Industry experience in medical technology or pharma is required 6+ years of experience in Scientific or Medical Writing, relevant academic or clinical research experience (Masters or PhD) is preferred. Expertise in interpreting information clearly and accurately to concisely communicate results and recommendations to stakeholders, senior management, and their teams.  

Responsibilities Develop and implement multi-channel engagement (MCE) strategies to support the organization’s goals and objectives. Manage and oversee all aspects of MCE programs, including needs assessments, program development, implementation, and evaluation. Monitor and analyze engagement metrics to optimize and improve engagement strategies and tactics. Collaborate with internal and external partners, including Key Opinion Leaders (KOLs) and medical societies, to support MCE initiatives. Ensure that all MCE programs and materials are compliant with regulatory guidelines and standards. Stay up to date with current trends and best practices in multi-channel engagement.   Qualification & Experience 2+ years of experience in multi-channel engagement within the pharmaceutical or biotech industry. A bachelor’s or master’s Degree in a scientific or healthcare-related field. Strong project management skills, with the ability to manage multiple projects simultaneously. Excellent communication and presentation skills, with the ability to effectively communicate complex medical information to diverse audiences. Experience working with internal and external stakeholders, including key opinion leaders and medical societies. A strong understanding of regulatory guidelines and standards for multi-channel engagement.  

Responsibilities Effectively collect and evaluate data, information, and input from multiple sources, functions, and regions to create a cohesive content strategy for writing projects. Plan (including organizing/preparing outlines), write (including first-draft authoring), edit, review, coordinate, and complete the regulatory documents supporting clinical development/product registration. Conduct effective document initiation meeting to ensure authoring team alignment and understanding. Build scientific-based rationale that support the purpose of more complex and/or strategic documents. Ensure data are presented in a clear, complete, accurate, and concise manner. Ensure that key data, statements and conclusions are consistent across related documents, and that statements and conclusions are integrated, accurate, balanced and supported by appropriate data. Coordinate expert/scientific reviews, collate reviewer’s comments, adjust content of document as required based on internal/external input, and prepare final version. Ensure and coordinate quality checks for accuracy. Exhibit flexibility in moving across development and preparation of multiple document types. Influence or negotiate change of timelines and content with other team members. Work with internal and external experts to develop and prepare presentations. As needed, may build and manage relationships with vendors/alliance partners. Lead the writing process and apply effective project management skills to ensure timely completion of high-quality regulatory documents. Build/communicate credible writing project timelines. Anticipate and mitigate risks to delivery Work with teams and stakeholders to ensure smooth and timely development of documents and escalate issues, as appropriate, to ensure document completion. Effectively communicate project status to stakeholders  

Responsibilities Manage, oversee and facilitate product transition activities across GMA-DK and GMA-BLR; managing, tracking and reporting on key milestones. Ensure excellent project management, oversight and execution of strategic projects and initiatives. Identify and drive initiatives for optimising ways of working and implement process improvements. Collaborate closely with Business Partners in GMA-DK, especially those managing products in transition. Oversee and manage project budgets in collaboration with key stakeholders.   Qualification & Experience Bachelors/master’s degree in life sciences, business or relevant area. 6+ years of relevant work experience in cross functional Project Management or Consulting in the pharma industry. Experience in and understanding of Medical Affairs, preferred. Should have a passion for project management, stakeholder engagement and understand the link between science and business in the Pharma industry.  

Responsibilities Provide specialized cardiac care to patients Give health advice to patients Prescribe treatments Monitor patients Collaborate with a team of healthcare professionals Participate in medical research and education activities Stay updated with the latest advancements in the field of cardiology     Qualification & Experience Medical degree with specialization in Cardiology 7 to 10 years of experience in a similar role Detail-oriented and able to handle complex medical cases Strong interpersonal and communication skills  

Responsibilities Dispensing prescription medications accurately and efficiently Checking prescriptions for proper dosage and ensuring interactions with other medications are identified and addressed Reviewing patients' medical records to monitor medication therapy and identify potential drug-related problems Providing medication counseling to patients on proper medication use, possible side effects, and potential drug interactions Collaborating with healthcare professionals to develop and implement patient care plans Ordering, storing, and maintaining an adequate inventory of medications and supplies Maintaining accurate and confidential patient records Ensuring compliance with relevant pharmacy laws, regulations, and standards Participating in continuous education and professional development activities     Qualification & Experience Bachelor's degree in Pharmacy Registered Pharmacist in Karnataka Minimum of 10 years of experience as a Pharmacist Strong knowledge of pharmaceutical guidelines, laws, and regulations Excellent communication and interpersonal skills  

Responsibiliities Cleanliness of the entire laboratory area Collection and distribution of specimens from the various collection points Dispatch of all completed reports to concerned wards /sections/common OPD distribution point Run errands for the lab services Labeling of different specimen containers. Replenish sample / specimen collection points with fresh specimen / sample containers Perform job requirements as per departmental protocols Maintain individual accountability for the equipment and items in the labs. Clean all expended sample/specimen container and disinfect/autoclave and dispose of lab waste / specimens as per Waste Management Protocols. Fumigate lab area as per requirements laid down. Any other jobs assigned as per exigencies of work    

Responsibilities Develop comprehensive understanding of the Lilly’s Therapeutic areas, Establish and lead a cross-functional team, be a scientific thought leader for the group to enable effective and efficient delivery of high-quality clinical outcomes with aggressive metrics. Effectively and efficiently deliver the business unit portfolio with quality, on-time Participate in strategy development and monitor metrics for on-time delivery of statistical support Assess demand for resources, prioritize work, and resolve issues related to scope of work Coordinate resource allocation and tracking for internal and outsourced projects Communicate and resolve issues related to statistics with appropriate level of customer team personnel Partner with Global leaders in driving project decisions related to clinical data execution options Partner closely with other development and administrative functions to effectively plan, forecast, and manage the resources required to deliver all sanctioned projects Develop deep therapeutic area expertise within LCCI teams Establish deep technical capabilities at LCCI with supervision of direct reports and a total staff comprised of diverse skill set accountable for hands-on statistical activities Develop strategies and build, capabilities and expertise within the team catering to advanced statistical capabilities Build-up, maintain and foster deep therapeutic, scientific excellence and environmental expertise to ensure accountability and proactive ability to deliver specific business needs     Qualification & Experience M.S. or Ph.D. in Statistics/Biostatistics Minimum of 10 years of industry experience Broad knowledge of the drug development process which includes industry requirements, quality expectations, and practices.  

Responsibilities Contribute to the development, evaluation, coordination and maintenance of global educational modules & educational offerings in partnership with medical stakeholders/subject matter experts, to meet GSK medical capability needs and Continuing Professional Development (CPD) requirements. Play a critical role in co ordinating the education operational activities of the Academy of Pharmaceutical Medicine and the Virtual Academy. Schedule, advertise and co-ordinate education modules including face to face courses and virtual seminars. Provide day-to-day learning administrative support and coordination in relation to learning preparation, administration, follow-up and reporting to deliver high quality, timely and easily accessible learning services. Maintain education operation activities in the Learning Management system to include creation of learning items related to capability development areas, assign curricula and learning items to groups of staff in line with business requirements. Maintain education offerings in Virtual Academy to include updating training plans and the Events Centre. Partner with Subject Matter Experts to ensure understanding of the implications of how Learning is administered. Archive course material/documentation in accordance with requirements and where required, upload online content to the learning management system. Network with other Training Co-ordinators across GSK to share best practice and maintain current system knowledge. Support the development and deployment of ‘Virtual’ learning technologies including e-learning development, Live Meeting content/meeting management and blended/distance learning programs.   Qualification & Experience Associate degree Experience managing learning projects involving physician/scientific professional development & postgraduate training Experience developing and delivering learning content, improving efficiency and quality of outputs Experience diagnosing, developing and implementing solutions for challenges with learning needs