39 Medidata Jobs in Eluru

Dear Candidates,  Currently we are hiring fresher Graduates or post Graduates in Top Reputed Bank as Relationship Officer.  Guntur,Vijayawada,Eluru and Rajahmundry  The candidates have to go outside and verify the KYC documents and then they have to Cross Sell the banking products like Current Accounts and savings accounts.  Candidates must have Graduation/PG and Bike+DL.  Age must be less than 27 Years.  CTC- Upto 3LPA+ Incentives  Candidates who are interested in sales.  Please contact 7032171117

Hiring for Life Insurance, as a .Relationship Manager Bancassurance. Salaries upto 4.2 lacs. Plus Allowances plus Incentives(average Rs 10000 per month). Interested can apply. This is an immediate requirement! Pls share your CV with ______1. Send me resume2.CTC 3. Location -Narasaraopet, ongole, Eluru, Kondepi, Sompet need exp in banking / insurance  Age -33

As a RAVE Database Build Programmer at [Your Company Name], your role will involve designing, building, and managing clinical trial databases using Medidata RAVE. You will collaborate with cross-functional teams to ensure databases align with protocol requirements, maintain high-quality standards, and support the successful execution of clinical studies. Key Responsibilities: - Design and build clinical trial databases in Medidata RAVE. - Create and configure eCRFs (electronic Case Report Forms) and program edit checks. - Implement and test custom functions using C# scripting. - Manage data validation, cleaning, and handling processes. - Perform User Acceptance Testing (UAT) and ensure database accuracy. - Handle protocol amendments, mid-study updates, and database migrations. - Integrate RAVE with other clinical trial systems (e.g., SAS, CTMS). - Manage user roles, permissions, version control, and deployment. - Provide support for audit trail management and compliance. - Troubleshoot and resolve database issues. Qualifications: - 3+ years of experience in clinical database programming, preferably with Medidata RAVE. - Strong understanding of clinical trial processes and data management. - Proficiency in C# for custom function programming. - Experience with query management, edit check programming, and form design. - Familiarity with regulatory requirements (e.g., 21 CFR Part 11). - Excellent problem-solving and communication skills. - Ability to work independently and collaboratively in a fast-paced environment. If you are passionate about clinical research and have a knack for database programming, [Your Company Name] offers you the opportunity to work on cutting-edge clinical trials in a collaborative and supportive team environment. You will also benefit from a competitive compensation and benefits package, along with career growth and development opportunities. We look forward to hearing from you!,

As a Rave Custom Function Programmer, your role will involve developing and maintaining Medidata Rave Edit Checks and Custom Functions using C# based on Data Validation Specifications aligned with client requirements. You should possess a strong understanding of Electronic Data Capture (EDC) systems and Good Clinical Practices (GCP) to perform post-production changes and troubleshoot operational issues. Collaboration with cross-functional teams to define timelines, responsibilities, and deliverables will be a key aspect of your work. Additionally, building internal tools and metrics dashboards using platforms like Excel and Visual Studio to support quality and performance tracking will be part of your responsibilities. You are expected to work independently with minimal supervision, showcasing a solid understanding of coding, development processes, and problem-solving in a clinical data environment. Key Responsibilities: - Develop and maintain Medidata Rave Edit Checks and Custom Functions using C# based on Data Validation Specifications - Possess a strong understanding of EDC systems and GCP to troubleshoot operational issues - Collaborate with cross-functional teams to define timelines, responsibilities, and deliverables - Build internal tools and metrics dashboards using platforms like Excel and Visual Studio - Work independently with minimal supervision, demonstrating coding expertise in a clinical data environment Qualifications Required: - Bachelor's Degree in Computer Science or related discipline - 2 years of application programming experience, preferably with a strong technical skill set in C#.Net - Experience in Medidata Rave Edit Checks and Custom Functions using C# Please note that the job location for this role is Pan India, and the work mode is Hybrid. As a Rave Custom Function Programmer, your role will involve developing and maintaining Medidata Rave Edit Checks and Custom Functions using C# based on Data Validation Specifications aligned with client requirements. You should possess a strong understanding of Electronic Data Capture (EDC) systems and Good Clinical Practices (GCP) to perform post-production changes and troubleshoot operational issues. Collaboration with cross-functional teams to define timelines, responsibilities, and deliverables will be a key aspect of your work. Additionally, building internal tools and metrics dashboards using platforms like Excel and Visual Studio to support quality and performance tracking will be part of your responsibilities. You are expected to work independently with minimal supervision, showcasing a solid understanding of coding, development processes, and problem-solving in a clinical data environment. Key Responsibilities: - Develop and maintain Medidata Rave Edit Checks and Custom Functions using C# based on Data Validation Specifications - Possess a strong understanding of EDC systems and GCP to troubleshoot operational issues - Collaborate with cross-functional teams to define timelines, responsibilities, and deliverables - Build internal tools and metrics dashboards using platforms like Excel and Visual Studio - Work independently with minimal supervision, demonstrating coding expertise in a clinical data environment Qualifications Required: - Bachelor's Degree in Computer Science or related discipline - 2 years of application programming experience, preferably with a strong technical skill set in C#.Net - Experience in Medidata Rave Edit Checks and Custom Functions using C# Please note that the job location for this role is Pan India, and the work mode is Hybrid.

As the Leader, HRBP Operations for R&D and SCM at Lixil India's factory site in Bhimadole near Eluru District, Andhra Pradesh, your primary role is to act as a strategic HR Business Partner for Operations, Research & Development, and Supply Chain Management in India. Your responsibilities include providing strategic consulting on people strategies, organization design, performance management, organizational culture, employee engagement, and labor relations to the appointed plants to contribute to business performance. - Serve as a strategic business partner and advisor aligning people strategies with business objectives, driving change management initiatives for organizational effectiveness. - Formulate comprehensive HR solutions based on plants/functions goals, challenges, and root cause analysis, gaining buy-in from key stakeholders to achieve goals effectively. - Drive HR Excellence to create a meaningful employee experience through attraction, performance, retention, and development. - Utilize integrated HR platforms and databases with dynamic data analytics to provide workforce insights, manage HC, AOP budget, and ensure cost efficiency. - Develop organizational and people capabilities fostering a learning culture, consult with plant/function leaders to build a talent pipeline meeting business needs. - Implement high standards of performance management to enhance individual performance and foster a performance-driven culture contributing to plant productivity. - Ensure a fully compliant working culture, guide team in managing plant administration responsibilities including vendor management, cost management, and employee plant admin experience. - Demonstrate willingness to challenge the status quo and accept stretched assignments. Qualifications: - Minimum 10 to 15 years of relevant HRBP experience in a multinational company, operational environment experience preferred. - 5 years of leadership experience. - Masters/Bachelors Degree or above in HR or Administration. - High integrity and adherence to Lixil compliance requirements and values. Note: This profile may require travel up to 15% to engage with the team working for India assembly lines and SCM team in Mumbai and Gurgaon.,

As a Custom Function Programmer, you will be responsible for developing custom functions and working with Medidata Rave and C#. Your key responsibilities will include: - Developing custom functions for specified requirements - Collaborating with the team to integrate custom functions into Medidata Rave system The qualification required for this role includes: - Minimum 5 years of experience in custom functions development - Proficiency in Medidata Rave and C# programming,

As an Implementation Consultant at our company, your role will involve the following key responsibilities: - Responsible for creating User Requirement Specifications (URS) and functional requirement specs in Clinical Reporting and Analytics. - Create wire-frames and mock-ups for Clinical reports. - Communicate with Clinical Data Management & Medical Reviewers to document the clinical reporting needs. - Stay up-to-date with all Saama product features and releases. - Analyze and understand current business processes, events, and flows in Clinical Trial Development. - Act as a Clinical Subject Matter Expert and provide Clinical Project Support. - Author and document business requirements, providing analytical support needed to translate requirements into solutions. - Create and maintain Data Mapping Specifications for Saama Data Review Model. - Incorporate feedback from customers, partners, and in-house teams on product. - Manage all aspects of projects related to implementation including guiding the client through release planning, managing communication, leading product implementation efforts, managing project team deliverables, documenting and reporting status and issues, identifying and managing risks, and acting as a client liaison. - Ensure a smooth transition of services from implementation to support. - Provide advanced analytical and reporting support to customers on various projects, solving complex problems and conducting complex analysis. - Support configuration and quality check with project teams to ensure the solution meets business objectives. - Help identify and define new sources of relevant data, analyze data, and make recommendations. - Support customer User Acceptance Testing (UAT) phase for any configuration change or issue triaging. - Understand and discuss the application and implications of changes to the process and relation to requirements. Desired Skills: - Experience in the Pharmaceutical industry is essential. - Good understanding of Clinical Systems such as EDC Systems (Medidata Rave, Veeva EDC, Oracle InForm, etc.), CTMS Systems (Siebel CTMS, Medidata CTMS, Veeva CTMS, etc.), IRT Systems (YPRIME, Parexel Clinphone, etc.), and LAB Systems (central Lab, local Labs, etc.). - Good experience in SQL. - Good understanding of the clinical trial domain, overall EDC study setup, and Clinical reporting. - Experience in building Clinical reports and dashboards. - Understanding of CDASH, SDTM, and ADAM standards. - Relevant degrees such as Bachelor's and Master's Degree in Healthcare, Computer Science, Technical, Engineering, Computer, Computer Engineering, Computer Programming - Bachelor's degree (BA) in computer science or equivalent work experience required. - 1-2 years of experience as a Product Owner. - Comfortable and familiar with the Agile Working Environment. - Experience working with all phases of Software Development Life Cycle (SDLC). - Familiarity with FDA regulations such as 21 CFR Part 11 and GxP is a bonus. - Experience working in the complete product life cycle of two or more products. - Technical knowledge including knowledge of Software Development and Web Development. - Experience with use and configuration of healthcare software applications (preferably clinical). As an Implementation Consultant at our company, your role will involve the following key responsibilities: - Responsible for creating User Requirement Specifications (URS) and functional requirement specs in Clinical Reporting and Analytics. - Create wire-frames and mock-ups for Clinical reports. - Communicate with Clinical Data Management & Medical Reviewers to document the clinical reporting needs. - Stay up-to-date with all Saama product features and releases. - Analyze and understand current business processes, events, and flows in Clinical Trial Development. - Act as a Clinical Subject Matter Expert and provide Clinical Project Support. - Author and document business requirements, providing analytical support needed to translate requirements into solutions. - Create and maintain Data Mapping Specifications for Saama Data Review Model. - Incorporate feedback from customers, partners, and in-house teams on product. - Manage all aspects of projects related to implementation including guiding the client through release planning, managing communication, leading product implementation efforts, managing project team deliverables, documenting and reporting status and issues, identifying and managing risks, and acting as a client liaison. - Ensure a smooth transition of services from implementation to support. - Provide advanced analytical and reporting support to customers on various projects, solving complex problems and conducting complex analysis. - Support configuration and quality check with project teams to ensure the solution meets business objectives. - Help identify and define new sources of relevant data, analyze data, and make recommendations. - Support customer User Acceptance Testing (UAT) phase f

As an aspiring candidate for the position, you will be responsible for achieving business targets by acquiring new client relationships and maintaining them effectively. Your role will involve the following key responsibilities: - Identify target areas for prospective business - Pre-screen customer segments in line with organizational norms - Ensure a satisfactory number of logins and disbursements - Proactively understand customer needs to ensure a high level of customer satisfaction, cross-selling multiple products as required - Execute sales promotion activities to generate customer interest in the TCFSL brand - Cultivate strong client relationships internally and externally, fostering a robust brand identification with potential customers - Facilitate vendor empanelment and establish relationships with new vendors - Develop and maintain strong distribution channels - Ensure compliance with all Audit and RBI regulations. You are required to be a graduate in any discipline to be eligible for this position.,

You will be working as a Clinical Data Svs Sr Analyst at Accenture, a global professional services company with leading capabilities in digital, cloud, and security across more than 40 industries. Your role will be aligned with the Life Sciences R&D vertical, focusing on clinical data management activities including discrepancy review, query generation, resolution, creating CRF Completion Guidelines (CCG), SAE reconciliation guidelines, and managing clinical data management projects. Your responsibilities will include developing clinical study databases, building electronic case report forms, programming edit checks, and supporting updates or changes to the study database. **Key Responsibilities:** - Overall experience of 4+ years with exposure to EDC platforms like Medidata RAVE EDC, Inform, Oracle Clinical, Veeva, etc. is preferred - Extensive experience in database design, edit check programming, custom function programming, and unit testing - Experienced in various modules such as IVRS/RWS integration and Lab administration - Medidata RAVE study builder certification is preferred **Qualifications Required:** - BSc or Master of Pharmacy You should be adaptable, flexible, able to perform under pressure, have problem-solving skills, detail orientation, and the ability to establish strong client relationships.,

As a Clinical Data Services Analyst at Accenture, you will be involved in the Clinical Data Management team focusing on the collection, integration, and availability of data at appropriate quality and cost. Your role will include performing data management activities such as discrepancy review, query generation, and resolution. You will also be responsible for creating CRF Completion Guidelines (CCG) and SAE reconciliation guidelines. Additionally, you will help in identifying and raising protocol deviations in the database, performing edit check validation, writing test scripts, and carrying out database validation (UAT) against the specified CRF/ECRF. Your responsibilities will also involve managing clinical data management projects. **Key Responsibilities:** - Develop clinical study databases by building electronic case report forms and programming edit checks as per specifications. - Support any updates or changes to the study database (e.g., Protocol amendments) through the change control process. **Qualifications Required:** - BSc/Master of Pharmacy - 3 to 5 years of experience - Language proficiency in English (International) at an expert level About Accenture: Accenture is a global professional services company with leading capabilities in digital, cloud, and security. With over 699,000 employees serving clients in more than 120 countries, Accenture offers Strategy and Consulting, Technology and Operations services, all powered by the world's largest network of Advanced Technology and Intelligent Operations centers. The company embraces the power of change to create value and shared success for its clients, people, shareholders, partners, and communities. For more information, visit www.accenture.com. In your role, you will be aligned with the Life Sciences R&D vertical at Accenture, where services span across the entire life sciences enterprise. Employees in this vertical work on various sub-offerings like Clinical, Pharmacovigilance & Regulatory, helping leading biopharma companies bring their vision to life by improving outcomes through patient-centric approaches and scientific expertise. **What We Are Looking For:** - Adaptable and flexible individuals - Ability to perform under pressure - Strong problem-solving skills - Detail-oriented approach - Capability to establish strong client relationships If you are a Clinical Database Developer with over 4 years of experience and exposure to EDC platforms like Medidata RAVE EDC, Inform, Oracle Clinical, Veeva, etc., this role is ideal for you. You should have extensive experience in database design, edit check programming, custom function programming, and unit testing. Certification in Medidata RAVE study builder would be preferred. Additionally, experience in various modules such as IVRS/RWS integration and Lab administration will be beneficial.,

As a Content Writer Intern at Savidha Digital in Eluru, your role involves writing engaging content for social media, blogs, and campaigns. You will be responsible for creating catchy captions, taglines, and ad copies for various brands. Additionally, you will collaborate with the design and marketing teams to brainstorm creative ideas and contribute to campaign planning and storytelling strategies. Key Responsibilities: - Write engaging content for social media, blogs, and campaigns - Create catchy captions, taglines, and ad copies for various brands - Brainstorm creative ideas with the design and marketing teams - Contribute to campaign planning and storytelling strategies Qualifications Required: - Strong writing skills and creativity - Passion for social media and digital trends - Attention to detail and willingness to learn - Positive attitude and team spirit If you excel in this role, you will receive an Internship Certificate, mentorship, and learning opportunities. High performers may also have the opportunity to secure a full-time position at Savidha Digital. If you are enthusiastic about writing, social media, and storytelling, apply now by sending your resume and writing sample to lalitha@savidhadigital.com.,

As an Associate Data Manager on a Fixed Term Contract in India with Premier Research's Functional Services Provider (FSP) team, you play a crucial role in supporting biotech, medtech, and specialty pharma companies in translating groundbreaking ideas and cutting-edge science into life-saving medicines, devices, and diagnostics. Your contributions directly impact the lives of patients, making you an essential part of the team. - Assist in ensuring clean databases by reviewing clinical trial data for compliance with protocol and Data Management Plan guidelines - Provide input to and review Data Management Plans for clinical study deliverables - Review and address queries, resolve discrepancies, and update the database accordingly - Support data entry and query testing for accurate data input and identification of potential data anomalies - Assist in user acceptance testing for study-specific data listings to validate data output compliance with requirements - Prepare and maintain documentation related to CRF, edit check, and data listing testing, ensuring necessary changes are implemented - Bachelor's degree or international equivalent in a technical, clinical, or health-related field, or equivalent combination of education, training, and experience - Ideally, 1 to 2 years of experience with commercial clinical data management systems or EDC products (e.g., Oracle RDC/Inform, Medidata Rave, DataLabs) or proven experience in primary job functions - Strong English verbal and written communication skills - Proficiency in Microsoft Windows environment and Microsoft Office Suite tools - Ability to deliver a positive customer experience through effective communication, timely deliverables, and task ownership - Strong analytical and organizational skills, with the ability to work independently and manage multiple projects in a fast-paced environment Premier Research values your contribution and is committed to helping you grow both professionally and personally. Your voice matters here, influencing the way we work and delivering medical innovation that patients urgently need. Join Premier Research and shape your future in the biotech industry.,

As a Research & Development Consultant in Life Sciences at Accenture, you will be responsible for leveraging your expertise in R&D, Pharmacovigilance, and regulatory reporting to drive impactful solutions for clients. Your role will involve the following key responsibilities: - MBA from a Tier 1 institute or significant relevant industry experience - 6+ years of progressive business and/or consulting experience, with at least 1 year in the Life Sciences industry - Management consulting and general business consulting background is essential - Proficiency in utilizing assets and tools in business consulting (R&D), including issue trees, implementation frameworks, diagnosis tools, operating models, and business process mapping - Experience working with R&D functions such as Laboratory functions, clinical operations, pharmacovigilance, regulatory affairs, and quality management system - Familiarity with clinical data management platforms like Medidata/RAVE, Veeva Clinical suite, pharmacovigilance databases (ArisG & ARGUS), Regulatory Information Management Systems (Veeva RIM), and lab informatics is desirable As an industry expert, you will play a vital role in providing strategic insights and innovative solutions to our clients in the Life Sciences sector. Join us at Accenture, where you will have the opportunity to make a meaningful impact and drive positive change in the industry. As a Research & Development Consultant in Life Sciences at Accenture, you will be responsible for leveraging your expertise in R&D, Pharmacovigilance, and regulatory reporting to drive impactful solutions for clients. Your role will involve the following key responsibilities: - MBA from a Tier 1 institute or significant relevant industry experience - 6+ years of progressive business and/or consulting experience, with at least 1 year in the Life Sciences industry - Management consulting and general business consulting background is essential - Proficiency in utilizing assets and tools in business consulting (R&D), including issue trees, implementation frameworks, diagnosis tools, operating models, and business process mapping - Experience working with R&D functions such as Laboratory functions, clinical operations, pharmacovigilance, regulatory affairs, and quality management system - Familiarity with clinical data management platforms like Medidata/RAVE, Veeva Clinical suite, pharmacovigilance databases (ArisG & ARGUS), Regulatory Information Management Systems (Veeva RIM), and lab informatics is desirable As an industry expert, you will play a vital role in providing strategic insights and innovative solutions to our clients in the Life Sciences sector. Join us at Accenture, where you will have the opportunity to make a meaningful impact and drive positive change in the industry.

As a business-focused Enterprise Solutions Architect with extensive experience in the pharmaceutical value chain, you will collaborate with Pharma and CRO clients to shape digital solutions, lead proposal development, and develop transformative strategies using AI, data, and platform-centric innovations. Your key responsibilities will include: - Leading solutioning activities across the Pharma value chain, involving digitization of pre-clinical and clinical trials, optimization of clinical operations, automation of lab processes, modernization of CRO workflows, integration and analytics of real-world data, and development of commercial analytics and omnichannel launch strategies. - Shaping data-centric solutions incorporating structured/unstructured clinical and real-world data with cloud-native architectures and AI enablement. - Ideating AI/ML-enabled or NextGen solutions for trial optimization, patient journey analytics, digital twin use cases, brand performance forecasting, and medical rep targeting. - Developing proposals, solution POVs, and reusable digital assets for Pharma and CRO clients. - Collaborating with delivery, product, and platform teams to co-develop ready-to-deploy solution frameworks and demos. - Contributing to Go-To-Market (GTM) initiatives by creating internal playbooks, sales kits, and co-innovation plans. Qualifications Required: - Bachelors or Masters degree in Life Sciences, Pharmacy, Clinical Research, or Data/Engineering fields. - Minimum of 10 years of experience in pharma technology services, clinical systems, or commercial pharma analytics. - Deep understanding of end-to-end pharma processes, including clinical development, lab workflows, commercial ops, and data governance. - Experience in solutioning around platforms such as Medidata, Veeva Clinical Suite, Oracle Clinical, LabVantage, Spotfire, and Snowflake. - Strong knowledge of CRO operating models, including site engagement, monitoring, and data services. - Hands-on experience in developing solution architectures using cloud platforms (AWS, Azure), AI/ML frameworks, and analytics platforms.,

Role Overview: As a Commission Sales Associate based in Eluru with some work from home flexibility, your primary responsibility will be to generate sales, cultivate customer relationships, identify customer requirements, and offer appropriate electrical solutions. Your daily activities will include participating in meetings, initiating sales calls, delivering product details, negotiating agreements, and compiling sales reports. Key Responsibilities: - Generate sales by identifying potential customers and maintaining existing client relationships - Understand customer needs and provide suitable electrical solutions - Attend meetings to discuss sales strategies and objectives - Make sales calls to promote products and services - Present product information clearly and effectively to potential clients - Negotiate contracts and pricing to secure sales - Prepare and deliver informative sales reports to management Qualifications Required: - Possess sales and customer relationship management skills - Demonstrate excellent communication and presentation abilities - Exhibit strong negotiation and problem-solving capabilities - Have product knowledge in the electrical industry - Be self-motivated and driven to achieve targets - Previous experience in a sales role, particularly in the electrical sector, is advantageous - A Bachelor's degree in Business, Marketing, or a related field is preferred Please note: This position allows for part-time work, making it suitable for students seeking employment opportunities.,

As a Clinical Data Manager at Statistics & Data Corporation (SDC), your role will involve participating in all data management activities to support clinical and/or non-clinical research studies. You will work closely with lead Clinical Data Managers and/or Clinical Data Analysts to manage project activities throughout the lifecycle of the projects. Your primary responsibilities will include: - Independently performing study setup activities such as CRF design, database structure design, annotation, DMP, CRF completion guidelines, and data entry screen design - Serving as a primary or backup resource for data management issues - Assisting with management of timelines and communication related to data management activities - Collaborating with Clinical Data Analysts to ensure timely completion of study tasks - Supporting data listing review and query management activities at key milestones - Maintaining quality control of data, project deliverables, and closeouts - Facilitating the review of medical coding for validity and completeness - Adhering to SDC's quality system and data integrity & business ethics requirements - Performing other related duties incidental to the work described You should possess the following skills and qualifications: Required Skills: - Competent working knowledge of clinical trials and the clinical data management role - Excellent organizational and project management skills - Ability to work independently and take the lead on all OM activities - Strong written and verbal communication skills - Technical skills including EDC systems (Medidata Rave and/or iMedNet), Microsoft Office, CRF design, MS Project, and analytical capabilities - Familiarity with clinical trial design and regulatory guidelines (FDA/CFR, ICH/GCP) Education or Equivalent Experience: - Bachelor's degree and a minimum of four (4) years of experience in clinical data management, or an equivalent combination of relevant education and/or experience with current Certified Clinical Data Manager (CCDM) certification Statistics & Data Corporation (SDC) is committed to developing its employees, providing growth opportunities, career advancement, flexible work schedules, engaging work culture, and employee benefits. The company's recognition program is aligned with its core values, and it offers a place of belonging to employees with fun and engaging activities. SDC is dedicated to constant growth and innovation to support client and employee needs, with a proven track record of successfully executing client clinical programs since 2005. Join the SDC team to be a part of this dynamic and evolving industry.,

As a Mother Teacher at Siddhartha Quest CBSE School, located in Vatluru, Eluru, Andhra Pradesh, you will play a crucial role in providing a nurturing and stimulating learning environment for young minds in Grades 1 & 2. Utilizing the Mother Teacher approach, you will focus on subjects like English, Mathematics, and Environmental Studies (EVS) to ensure consistent care, emotional support, and holistic development for the students. - **Teach English, Mathematics, and Environmental Studies (EVS) in a child-friendly and engaging manner following the CBSE curriculum. - Implement phonics-based teaching methods to enhance early literacy and language development. - Create an interactive and activity-based learning environment to make learning enjoyable and effective. - Foster a safe, caring, and disciplined classroom atmosphere that supports young learners. - Use storytelling, hands-on activities, play-based learning, and technology integration to enhance understanding. - Conduct regular assessments, progress tracking, and personalized learning plans for students. - Maintain strong communication with parents to ensure collaborative learning and overall student well-being. - Organize and participate in co-curricular activities, classroom events, and school celebrations. - Collaborate with co-teachers, coordinators, and school management to ensure high-quality education delivery. - **Educational Qualification: B.Ed./D.El.Ed./NTT with a relevant Bachelor's degree. - Experience: Minimum 3 years of experience in early primary teaching. - Skills required: - Strong phonics knowledge and ability to teach early reading skills effectively. - Excellent communication and storytelling skills. - Patience, creativity, and empathy towards young learners. - Good command over English and regional languages (Telugu/Hindi preferred). - Basic knowledge of computer skills & technology-driven teaching methods. Join Siddhartha Quest CBSE School to work in a serene and green 5-acre campus that promotes a healthy learning environment. You will have the opportunity to be part of a progressive CBSE-affiliated school with modern infrastructure and teaching aids, nurturing young learners in an innovative and child-friendly environment. Additionally, you will benefit from supportive management that encourages your professional growth and development.,

Role Overview: As a PGT Physical Science (Physics & Chemistry) Teacher at Siddhartha Quest CBSE School in Vatluru, Eluru, Andhra Pradesh, your primary responsibility is to teach students in Grades 8, 9, and 10. Your role requires you to possess strong subject knowledge, exceptional teaching abilities, and a dedication to fostering a positive and engaging learning atmosphere. Key Responsibilities: - Plan and deliver captivating lessons in Physics and Chemistry adhering to the CBSE curriculum. - Create lesson plans, educational materials, and evaluation methods to support effective learning outcomes. - Implement innovative teaching techniques like experiments, practical demonstrations, and technology integration. - Prepare students for CBSE board exams by emphasizing conceptual comprehension and application-based learning. - Conduct regular assessments, provide constructive feedback, and track student progress. - Supervise laboratory activities to enhance practical understanding. - Encourage student participation in science exhibitions, Olympiads, and academic contests. - Maintain discipline and cultivate an enriching classroom environment that stimulates curiosity and problem-solving skills. - Collaborate with colleagues, participate in staff meetings, and engage in school activities. - Stay updated on advancements in the subject and incorporate best teaching practices. Qualifications & Experience: - Educational Qualification: M.Sc. in Physics/Chemistry (or related field) with B.Ed. (compulsory). - Experience: Minimum of 5 years of teaching experience at the secondary school level (CBSE background preferred). Skills Required: - Profound subject knowledge in Physics and Chemistry. - Outstanding communication and classroom management abilities. - Capability to engage students through interactive and hands-on learning methodologies. - Proficiency in utilizing digital tools and technology for teaching. - Enthusiasm for mentoring students and guiding them in their academic journey. (Note: The company provides a competitive salary ranging from 40,000 to 50,000 per month based on experience and qualifications. Accommodation is offered to outstation candidates. Additionally, the school offers professional development opportunities, training sessions, and a supportive work environment equipped with modern teaching resources.),

As a Mother Teacher at our CBSE school located at Eluru road, Near Vijayawada, Andhra Pradesh, your main role will be to plan and implement age-appropriate activities that promote the intellectual, social, and emotional development of children. You will create a safe and supportive learning environment that encourages exploration and discovery while developing and maintaining positive relationships with children, parents, and colleagues. Key Responsibilities: - Plan and implement age-appropriate activities for children. - Create a safe and supportive learning environment. - Develop and maintain positive relationships with children, parents, and colleagues. - Assess and record the progress of each child, providing feedback to parents. - Collaborate with other teachers and staff to create an effective educational program. - Attend parent-teacher meetings and actively participate in school events. - Stay updated on best practices in early childhood education. Qualifications Required: - Bachelor's degree in Early Childhood Education or a related field. - Montessori or Nursery Teacher Training Certification. - Proven experience as a Mother Teacher in a nursery setting. - Strong understanding of child development principles. - Excellent communication and interpersonal skills. - Patience, creativity, and a passion for working with young children. - Ability to create a positive and engaging learning atmosphere. In addition to the responsibilities and qualifications mentioned above, you will be provided with semi-furnished individual accommodation as part of the benefits package. This is a full-time, permanent position with Provident Fund benefits. The work schedule is in the morning shift, and proficiency in English is required for this role. Your work location will be in person at our school.,

Role Overview: As the Academic Affairs and Programme Officer for the Village & District Initiative located in Kovvali Village, Eluru, West Godavari District, Andhra Pradesh State, you will play a crucial role in leading and transforming the educational institution. Your responsibilities will involve overseeing the School and Intermediate College sections, ensuring academic excellence, competitive exam success, vocational readiness, and holistic student development within a village setting. Key Responsibilities: - Develop and embed a high-performance culture focused on achieving top ranks in competitive exams like IITs, Medical Colleges, and IAS/Civil Services examinations. - Act as a motivator, counsellor, and mentor for students to guide them towards high aspirations and competitive success. - Champion the use of websites, digital tutorials, and online classes to enhance students" understanding of core subjects. - Lead the design and continuous refinement of the curriculum, including the introduction of Vedic Mathematics classes and a focus on holistic well-being. - Strategically recruit, assess, and mentor passionate teachers to ensure a high standard of instruction. - Protect charitable interests by ensuring ethical resource management and strategic leadership. - Plan and oversee infrastructure requirements to effectively allocate resources and support student growth and retention. - Travel regularly to the village location or be stationed in the District Headquarters for effective oversight. Qualifications Required: - Mandatory prior experience in a senior educational leadership role. - Strong working knowledge of competitive entrance examinations and proven ability to achieve results. - Relevant advanced degree in Education or a related field preferred. - Results-driven mindset with a commitment to improving education in rural settings. - Demonstrated ability to manage projects and resources effectively under constraints. Additional Details: N/A,