39 Literature Review Jobs

As a Junior Researcher at NAIQ Brain Health in Chhattisgarh, India, your primary responsibility will involve conducting research on mental health issues, performing data analysis, and contributing to the development of AI-driven solutions. You will play a crucial role in enhancing mental health services through literature reviews, data analysis, and active participation in research projects. To excel in this role, you must possess strong research, data analysis, and literature review skills. A deep understanding of mental health issues and research methodologies is essential. Your analytical prowess and problem-solving abilities will be key assets in this position. Additionally, prior experience with AI-driven solutions would be advantageous. Effective written and verbal communication skills are crucial for this role as you will be required to convey complex findings and insights clearly. The ideal candidate should hold a Bachelor's or Master's degree in Engineering/ Science (Electronics/ Computer Science/ Electrical/ Biomedical) or Psychology, Neuroscience, Public Health, or a related field. Join NAIQ Brain Health and be part of a team dedicated to revolutionizing mental health services by providing personalized support for brain health. Your contributions will help make personalized brain health support accessible to individuals in today's fast-paced world.,

Position: Research Intern Food R&D (Unpaid) Location: Chennai (Preferred) We are looking for a motivated and detail-oriented Research Intern to join our innovative R&D team. This role is best suited for candidates with a background in Food Technology, Food Science , or related disciplines, and a keen interest in functional ingredients, nutraceuticals, and clean-label innovation. Key Responsibilities Conduct structured literature reviews on functional foods, nutraceuticals, and processing techniques using PubMed, Scopus, and Google Scholar. Analyze scientific data to support R&D decisions and ingredient evaluations. Track market trends in clean-label, sustainable, and health-focused product development. Assist in functionality testing and support formulation for stability, efficacy, and cost-efficiency. Document experimental findings, research outcomes, and lab observations thoroughly. Collaborate with cross-functional teams on formulation, process improvement, and innovation projects. Prepare technical reports, research summaries, and ingredient profiles for internal documentation. Required Qualifications & Skills Pursuing or completed B.Tech/M.Tech/M.Sc in Food Technology, Food Science, or a related field. Strong aptitude in literature review and familiarity with scientific databases/tools. Prior experience with scientific writing or research publications is a plus. Analytical, detail-focused, and scientifically curious. Comfortable working in dynamic, team-oriented R&D settings. Learning Outcomes Practical exposure to end-to-end food R&D processesfrom research to prototype development. Hands-on experience in scientific writing, data interpretation, and technical documentation. Deeper understanding of current consumer and market trends in health and wellness. Collaborative work experience across formulation, regulatory, and innovation teams. Foundational knowledge in food regulations, functional ingredients, and product analysis. Show more Show less

As a Manager, Medical Writing & Research Affairs at TECCRO, you will play a crucial role in preparing high-quality scientific documents, including clinical study reports, research papers, regulatory submissions, and publications for medical journals. Your responsibilities will involve collaborating closely with clinical and research teams to ensure that manuscripts meet publication standards for major medical journals and align with the latest scientific research and TECCRO's clinical objectives. Your role will also require you to conduct thorough literature reviews, contribute to the design of clinical trials, and stay updated with current scientific and clinical advancements in the fields of medical aesthetics, skincare, and clinical trials. Additionally, you will work closely with internal teams, including clinical researchers, data managers, and regulatory affairs, to support the alignment of documents with clinical objectives and regulatory standards. Your expertise in medical writing will be essential for supporting business development efforts, including proposal creation and client communication. You will also assist in the preparation of regulatory submissions, ensuring that scientific documents align with required formats and regulatory guidelines. To excel in this role, you should possess exceptional writing, editing, and proofreading skills with a meticulous attention to detail. A strong understanding of clinical research methodologies, regulatory guidelines, and Good Clinical Practices is required. Proficiency in using writing and reference management software, along with excellent collaboration skills, will be beneficial for effectively working across cross-functional teams. If you are a skilled medical writer with a passion for science and research, this role offers an exciting opportunity to contribute to the advancement of clinical research and academic publications within the growing field of medical aesthetics. TECCRO provides a competitive salary with performance-based incentives, opportunities for professional development, certifications, and career growth, along with a supportive and collaborative work environment focused on research excellence and innovation in clinical trials. Join us at TECCRO and be a part of driving scientific and technological innovation in the aesthetics industry!,

You will be responsible for providing support for medical safety management within the Patient Safety & Pharmacovigilance department. This includes conducting medical review and assessments of Individual Case Safety Reports (ICSR), aggregate reports, co-authoring safety documents, and assisting in providing safety input to regulatory and clinical documents, as well as ad-hoc Health Authority queries. Your role will involve creating quality deliverables within agreed timeframes and maintaining a high standard of accuracy in compliance with patient safety business rules, standard operating procedures, and global and local regulatory requirements. Additionally, you will be supporting in defining, developing, and implementing metrics, standards, and tools to efficiently oversee the performance of the Pharmacovigilance and Medical Devices Vigilance system in terms of medical review of safety cases and management of safety signals. Key Responsibilities: - Conduct medical review of ICSRs, including assessment of Literature cases and authoring of enhanced MAC. - Support safety lead in authoring medical assessment letters based on the bi-annual/six-monthly line listing. - Perform literature review of assigned articles and assist in the review of articles for inclusion in PBRER, DSUR, IB, etc. - Provide support to Therapeutic Areas as per business needs, including co-authoring safety documents and assisting in providing safety input to regulatory and clinical documents. - Assist in monitoring the safety profile of products, including activities such as literature review, medical review of individual cases, and medical evaluation of quality defects. - Co-author the PBRER and provide medical inputs to specific sections, including follow-up activities on HA assessment reports. - Contribute to the medical sections of DSUR, IB, labeling documents, Product Guidance Documents, and Expert Statements. - Support signal detection and evaluation activities for assigned products. - Assist in the preparation of Health Authority queries and other safety-related documents. - Act as a Subject Matter Expert for Medical Function processes and provide support during audits and inspections. - Collaborate with other Global Line Functions across Novartis and Third Parties to meet joint accountabilities. - Contribute to PV&PV initiatives and cross-functional projects to optimize medical review processes and quality. - Assist in the development and optimization of training materials and deliver training to Novartis staff and external stakeholders. Minimum Requirements: - Bachelor of Science in Pharmacy, Bachelor of Science in Nursing, PharmD, PhD in relevant field, or Medical Degree (MBBS or MD) required. - Minimum 3 years of experience in the pharmaceutical industry or related field. - Experience in safety document or medical writing, including proficiency in coding with MedDRA and WHO dictionaries. - Strong understanding of clinical trial methodology, ICH GCP, GVP guidelines, and medical terminology. - Attention to detail and quality focus. - Strong organizational and project management skills. - Excellent communication skills and ability to operate effectively in an international environment. - Good understanding of Human physiology, pharmacology, clinical study objectives, and the drug development process. - Technical understanding of Biomedical/Biostatistics concepts and strong problem-solving skills. - Good presentation skills. - Proficiency in computer skills, including creating spreadsheets, templates, presentations, and working with safety databases/applications. - Ability to work independently, under pressure, demonstrating initiative and flexibility through effective innovative leadership ability.,

As a Research Assistant at IIM Ahmedabad, you will have the opportunity to work closely with Prof. Sunil Maheshwari and Prof. Sanjay Verma in conducting detailed research and analysis within the infrastructure or energy sectors. Your main responsibilities will involve delving into topics such as energy efficiency, sustainability, renewable energy, infrastructure development, and environmental impact. Your tasks will include gathering and analyzing both qualitative and quantitative data from a variety of sources, including field surveys, case studies, and existing literature. You will be expected to compile comprehensive reports, research papers, and technical documents that outline your findings, conclusions, and recommendations. Additionally, you will need to stay updated on the latest trends, technologies, and developments in the energy and infrastructure fields through extensive literature reviews. Moreover, you will be responsible for preparing presentations that effectively communicate the outcomes of your research to internal teams, clients, and other stakeholders. You will also be involved in analyzing policies, regulatory frameworks, and emerging trends within the energy and infrastructure sectors. Ideal candidates for this position should hold a master's degree in a relevant field such as Civil Engineering, Energy Systems, Sustainable Infrastructure, or Environmental Engineering. Strong analytical, technical, and communication skills are essential to contribute effectively to our projects. While prior experience in the energy, infrastructure, or environmental research domain is preferred, freshers are also encouraged to apply. This is a 6-month appointment with the possibility of extension based on performance. The selected candidate will work from the IIM Ahmedabad campus, with access to the library and computer center. Accommodation outside the campus is to be managed by the candidate, as the campus is centrally located within Ahmedabad. Reporting directly to Prof. Sunil Maheshwari and Prof. Sanjay Verma, you will have the opportunity to grow and learn in a dynamic research environment. Compensation for this position will be based on the qualifications and experience of the candidate. If you are interested in this exciting opportunity, please submit your CV and cover letter via email to sunilm@iima.ac.in / shoeb@iima.ac.in before the deadline on 25th January, 2025.,

Roles and Responsibilities Candidate will be required to do desk research on various domains like English Literature, Social Science and Management and write academic content related to the same. Content in the form of scientific papers, research articles, review papers and literature review will need to be written. Knowledge of systematic literature review, APA citation style, Harvard referencing system would be an added advantage. Desired Candidate Profile An ideal candidate will be a MBA, PGDM, Master's in Marketing, Finance, HR, Project Management, Operations Management, or English Literature with excellent English writing skills. Desk research and ability to understand basics of statistical analysis will be an added advantage. Perks and Benefits PF, Monthly Grocery

Role & responsibilities Good knowledge About process research, ROS, synthetic chemistry To assist in literature, search for experimentation, and finding suitable reagents, and methods Maintaining lab records, and preparing proper as per GLP documentation. Housekeeping maintenance of Lab & specific hood To synthesize the impurities as per requirements in scheduled time period Process optimization, validation and assist demonstration of the process in plant for commercialization Performing experiments, analysing the results, and come up with simple and scalable process

Role: Medical Writer Shift: Rotation Shift Location: Chennai WFO In this role you will be responsible for: Developing high-quality, scientifically accurate medical and regulatory documents, including clinical study reports, protocols, brochures, and more. Creating clear, concise, and audience-appropriate medical content for healthcare professionals, regulatory agencies, and internal stakeholders. Conducting thorough research and literature reviews to ensure content accuracy and compliance with industry standards. Collaborating with subject matter experts, scientists, and regulatory teams to develop compelling and compliant medical writing materials. Adhering to client and regulatory guidelines (e.g., ICH, FDA, EMA) while ensuring consistency, accuracy, and scientific integrity in all documents. Reviewing and revising content based on feedback from reviewers and editors. Managing multiple writing projects simultaneously while meeting strict deadlines and quality standards. Supporting quality control and peer-review processes to ensure excellence in medical documentation. Requirements for this role include: A Bachelors, Masters, or Doctorate degree in Life Sciences, Medicine, Pharmacy, or a related field. 3+ years of experience in medical writing within the pharmaceutical, healthcare, or life sciences industries. Strong understanding of medical and scientific terminology, clinical research processes, and regulatory requirements. Excellent writing, editing, and verbal communication skills with a keen eye for detail. Experience in preparing clinical and regulatory documents, publications, and scientific communications. Ability to interpret and summarize complex scientific data for different audiences. Familiarity with industry guidelines (e.g., ICH, GCP, AMA, FDA, EMA). Proficiency in Microsoft Office Suite and reference management tools. Strong organizational skills, ability to multitask, and work independently under tight deadlines. Experience collaborating with cross-functional teams, including researchers, medical professionals, and regulatory experts.

Roles and Responsibilities Candidate will be required to do desk research on various domains like English Literature, Social Science and Management and write academic content related to the same. Content in the form of scientific papers, research articles, review papers and literature review will need to be written. Knowledge of systematic literature review, APA citation style, Harvard referencing system would be an added advantage. Desired Candidate Profile An ideal candidate will be a M.A>, M.Sc, MBA, PGDM, Master's in Marketing, Finance, HR, Project Management, Operations Management, or English Literature with excellent English writing skills. Desk research and ability to understand basics of statistical analysis will be an added advantage. Perks and Benefits PF, Monthly Grocery

Job Title: Research Associate (Finance & Marketing) Department: Research Cell Location: Mumbai Reporting to: HOD Research Cell Position Overview: The Research Associate will support the institutes research agenda by assisting faculty members in academic and applied research projects, contributing to research publications, organizing research-based events, and facilitating institutional research goals. The role is ideal for candidates planning to pursue doctoral studies or build a career in academia or consulting. Key Responsibilities: Research Assistance: Assist faculty in literature reviews, data collection, analysis, and interpretation. Support writing and formatting of research papers, case studies, working papers, and articles. • Help in preparing presentations, reports, and research proposals for funding agencies or conferences. Data Analysis & Management: Collect primary and secondary data using surveys, interviews, databases, or online resources. • Use statistical software (SPSS, R, STATA, Excel, or Python) for data analysis and visualization. • Maintain research data logs and ensure data integrity and confidentiality. Documentation & Reporting : Prepare periodic progress reports on research projects. Maintain documentation related to research grants, ethics approvals, and project deliverables. • Assist in citation management and referencing using tools like Zotero, Mendeley, or EndNote. Academic Contributions: Co-author or assist in publishing research papers in reputed journals and conferences. Contribute to development of case studies and teaching materials. Assist in editing and maintaining institutional research journals or newsletters. Event Coordination : Help organize research workshops, seminars, conferences, FDPs, and guest lectures. Coordinate with guest speakers, participants, and vendors for smooth execution. Other Responsibilities: • Keep up to date with recent trends, publications, and developments in business and management research. Support accreditation and ranking-related data collation and documentation. Perform other academic or administrative tasks as assigned. Qualifications : Ph.D. in Management, Commerce, Economics, Finance, or allied disciplines from a recognized university/institution. Preference given to candidates with NET/SET qualifications or research exposure. Familiarity with academic research methodology and tools Skills & Competencies: Strong written and verbal communication skills. Proficiency in MS Oice (Excel, Word, PowerPoint) and statistical/data tools. • Detail-oriented, organized, and self-motivated. • Ability to work collaboratively in a team and under deadlines. • Passion for research and academic growth

As a Medical Writer with our dynamic team, you will utilize your expertise in writing, editing, and reviewing scientific and medical content. Your primary responsibility will involve transforming intricate medical data and research findings into clear, accurate, and engaging documents suitable for various audiences, including healthcare professionals, regulatory bodies, and the general public. You will be expected to develop, write, and edit a diverse range of documents such as clinical study reports, regulatory submission documents, peer-reviewed publications, and educational materials. Your role will also involve generating high-quality manuscripts, abstracts, posters, and presentations for scientific conferences, journals, and other platforms. Collaboration is key in this role as you will work closely with researchers, clinicians, regulatory affairs professionals, and other stakeholders to ensure that all content aligns with regulatory standards, maintains scientific accuracy, and supports corporate objectives. Additionally, you will be responsible for preparing and revising documents for regulatory submissions, ensuring compliance with guidelines from regulatory bodies such as FDA, EMA, and ICH. Your tasks will also include conducting literature searches, reviewing existing medical research, and ensuring the accuracy and relevance of information to support content development. Quality assurance is crucial as you will be editing and proofreading content for clarity, consistency, accuracy, grammar, and adherence to style guides. Project management skills are essential as you will be managing timelines for multiple projects to ensure timely and efficient completion of tasks. Compliance with medical, ethical, and regulatory standards is a core requirement for this role. To qualify for this position, you should hold a degree in BAMS, BDS, MBBS, or Pharm D, along with a minimum of 2 years of experience in medical writing, medical coding, or a related field. Experience with regulatory documents is highly preferred. A strong understanding of clinical research, medical terminology, and regulatory guidelines is essential. Proficiency in Microsoft Office Suite, reference management software, and medical writing software is required. Excellent written and verbal communication skills are essential, with the ability to convey complex information clearly and concisely. Strong attention to detail, collaboration skills, and the capability to work independently and as part of a team in a fast-paced environment are also necessary. Exceptional command of the English language is required, and knowledge of additional languages is a plus. Desirable skills for this role include experience with writing for regulatory agencies, familiarity with scientific publishing and journal submission processes, knowledge of Good Clinical Practice (GCP), and experience with statistical analysis and interpretation of clinical data. This is a full-time, permanent position with benefits including provided food, health insurance, and Provident Fund. The work schedule is a day shift with a fixed location in person. The application deadline is 31/07/2025.,

What We Want You To Do Analyze and manage the NGS / Nanopore data using relevant pipelines. Develop customized pipelines and workflows and tweak current pipeline filters for NGS and Nanopor analysis Help in developing and executing various data management strategies Identify the databases, tools, catalogs, and their reliability in future and help the research team in data collection strategies. Interpret genetic sequence variations identified through the pipelines Check quality and accuracy of the data Work in conjunction with team members to ensure consistent result generation Work in conjunction with wet lab and tech teams to ensure smooth operations and development work Troubleshoot issues related to data analysis tools and software Review literature for new technologies in the field of Bioinformatics Write grants and papers in the company Creating documentation and maintaining it What Are We Looking In You PhD in Genetics/Genomics or related fields or 8+ years of experience in the field of human genomics/genetics Experience with building bioinformatics pipelines for various kinds of NGS data Assisting in drafting and completing manuscripts for publication Experience with handling various different databases and tools Perform statistical analysis on the datasets Comfortable working on Linux OS system Ability to read, interpret and curate scientific literature Excellent communication skills (oral and written) and attention to detail Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow, instructions, complete deadlines, and comply with company policies Experience of 1-2yrs+ in Python & experience of 3-5 yrs in Bash scripting Experience with pipeline orchestration tools (Nextflow or Snakemake) will be a bonus Skills: pipelines,pipeline orchestration tools (nextflow, snakemake),python,genomics,communication skills,bash scripting,ngs data analysis,linux,quality control,bioinformatics pipeline development,ngs,nanopore data analysis,genetics,literature review,bioinformatics pipelines,linux os,pipeline orchestration tools (nextflow or snakemake),grant writing,statistical analysis,genetic sequence interpretation,scientific literature interpretation,human genetics,bioinformatics,data management strategies,pipeline

The role of Consultant / Sr. Consultant - Scientific Writer involves preparing literature reviews, abstracts, posters, slide sets, and manuscripts (complex) by working with various data sources such as clinical study reports and patient profiles. You will be responsible for performing quality control (QC) checks and proofreading of the deliverables to ensure they meet customer expectations. It is essential to comply with and support the group's project management tools, standards, policies, and initiatives. Maintaining records for all assigned projects, including archiving, and ensuring audit, SOP, and training compliance are also key responsibilities. The ideal candidate should have expertise in literature review, abstracts, posters, slide sets, and manuscripts. Attention to detail and the ability to meet customer expectations are crucial for this role. This is a full-time, permanent position in the ITES/BPO/KPO industry under the functional area of Pharmaceuticals. The role falls under the outsourcing/Offshoring category. If you have a passion for scientific writing and possess the necessary skills in literature review, abstracts, posters, slide sets, and manuscripts, we encourage you to apply for this position. Job Code: GO/JC/21340/2025 Recruiter Name: Mithra D,

Research Analyst Strategic Market Access -SLR Focus Hybrid Bengaluru/Bangalore/Thane India Job Summary Our research analysts on the Strategic Market Access team are responsible for supporting the delivery of a range of evidence-generation and strategic projects to support our clients Essential Duties & Responsibilities Conducting systematic/targeted/structured literature review Developing and performing database searches and writing protocols for literature review Identifying relevant evidence for research questions (primary and secondary screening) Extracting, analyzing, and summarizing data from a range of sources for internal and external stakeholders Performing quality control checks to ensure data accuracy Summarizing literature review findings in a report/slide deck Providing writing support for HTA submissions and publications based on HEOR studies Communicating with the internal and external stakeholders to ensure smooth and timely execution of the project Experience, Skills, And Qualifications Experience in healthcare research and market access or related fields preferred Masters degree + in health policy, public health, health services research, health administration, health economics, or any other related science field Authored 1-2 manuscript/poster presentations, etc, on SLR is preferred Experience conducting systematic literature reviews is preferred (knowledge of PRISMA, Cochrane guidelines, searching databases) Solid understanding of different payer archetypes, health technology assessment, and market access Superior communication skills and the ability to question the status quo Ability to forge and effectively manage relationships with internal and external stakeholders Solid communication ability both verbally and in writing (preferably experience in publications or systematic review reports) Proactivity, responsiveness, and the ability to balance shifting priorities to ensure that timelines and objectives are met and expectations are exceeded Excellent problem-solving and critical-thinking skills Knowledgeable in reference software (EndNote) Proficient in MS365, including Word, Excel, PowerPoint, Outlook, and Teams Travel Requirements 10% Potential Global Travel About OPEN Health OPEN Health unites deep scientific knowledge with wide-ranging specialist expertise to unlock possibilities that improve health outcomes and patient wellbeing Working in partnership with our clients, we embrace our different perspectives and strengths to deliver fresh thinking and solutions that make a difference OPEN Health is a flexible global organization that solves complex healthcare challenges across HEOR and market access, medical communications and creative omnichannel campaigns What We Offer As a global organization, OPEN Health is committed to supporting our employees and their families through a comprehensive benefits program Competitive pay, generous paid vacation, holidays and more, across all our locations Ongoing training and development opportunities which foster and shape your individual career path An active and growing commitment to bettering the communities our employees call home through our Corporate Social Responsibility program The opportunity to thrive in a global, collaborative environment while working every day to improve health outcomes and patient well being Diverse, inclusive culture that encourages you to bring your whole self to work If we sound like the sort of business environment in which you would thrive, then we would love to hear from you OPEN Health does not discriminate on the basis of race, sex, colour, religion, age, national origin, marital status, disability, veteran status, genetic information, sexual orientation, gender identity or any other reason prohibited by law in provision of employment opportunities and benefits

As a bench scientist in our organization, you will be responsible for conducting experimentation and research in the area of formulation development, process development, regulatory affairs, and intellectual property for global markets. Your work will involve planning and executing experiments aligned with project milestones while applying scientific principles such as Quality by Design (QbD), Design of Experiments (DoE), statistics, and scale-up principles. You will be expected to analyze and interpret data from literature reviews effectively to support decision-making processes. Additionally, you will need to understand the intellectual property landscape, develop strategies, search for prior art, and establish proof of concept through experimentation. Collaboration with cross-functional teams including Manufacturing Science and Technology (MS&T), Quality Assurance (QA), Quality Control (QC), and production teams across different geographies will be crucial for technology transfer and timely execution of submission batches. Your role will also involve identifying challenges, bottlenecks in development, and providing mitigation proposals at various stages of product development. Furthermore, you will be responsible for problem-solving, prioritizing activities, conducting development trials, and ensuring alignment with established milestones. Clear communication with internal stakeholders, proactive identification of challenges or risks, and adherence to business unit Key Performance Indicators (KPIs) will be essential aspects of your role. On a day-to-day basis, you will work closely with the formulation development teams to achieve key milestones, conduct experiments following QbD principles, and prepare presentations at different stages of product development. Your tasks will include literature reviews, sourcing API and Excipients, conducting preformulation studies, executing development trials, interpreting analytical data, and preparing necessary documentation for regulatory submissions. To be successful in this role, you should hold a Ph.D. in Pharmaceutical Sciences with at least 1 year of experience or an M.Pharm in Pharmaceutical Sciences with a minimum of 3 years of experience from reputable universities. Prior experience in working with generic pharmaceuticals in regulated markets such as the US, EU, or Canada will be advantageous. Your commitment to personal accountability, effective work habits, continuous learning, and collaboration with internal teams will be instrumental in contributing to the success of our organization's mission to make good health more affordable and accessible globally.,

As a Clinical Evaluation Medical Writer at Medtronic, you will play a crucial role in developing and updating clinical evaluation documents to support CE Mark submissions and ensure compliance throughout the product lifecycle. Your work will involve close collaboration with cross-functional teams to gather and interpret data on device safety, performance, and benefit-risk according to MEDDEV 2.7/1 Rev. 4 and EU Regulation 2017/745. You will also be responsible for summarizing and disseminating clinical literature and other available data to share relevant evidence, while managing Medical Information activities. This includes tracking inquiries, monitoring key metrics, researching and responding to technical and clinical questions from internal teams and external healthcare professionals under the guidance of Clinical and Medical Affairs. Success in this role will require strong skills in scientific writing, literature review, data analysis, and clear communication, as well as a proactive and collaborative mindset. Your responsibilities may include independently creating and maintaining clinical evaluation documents in compliance with relevant regulations and company procedures, supporting Medical Information activities by responding to inquiries, conducting literature searches and reviews, reviewing scientific materials for accuracy and compliance, developing reports, identifying and reporting complaints or adverse events, and collaborating with key stakeholders to drive evidence-based scientific decisions. To excel in this position, you are required to have a mastery of a specialty area and full knowledge of industry practices, typically obtained through advanced education combined with experience. A Baccalaureate degree and a total of 8 years of experience with a minimum of 4 years of relevant experience, or an advanced degree with a minimum of 2 years of relevant experience are also required. Medtronic offers a competitive salary and flexible benefits package as part of its commitment to employees. The company values the contributions of its employees and offers various benefits, resources, and competitive compensation plans designed to support you at every career and life stage. The position is also eligible for a short-term incentive called the Medtronic Incentive Plan (MIP). Medtronic is a global leader in healthcare technology that aims to address the most challenging health problems facing humanity by seeking out innovative solutions. With a mission to alleviate pain, restore health, and extend life, Medtronic unites a global team of passionate individuals who are committed to making a difference. The company values diversity and is dedicated to engineering extraordinary solutions for real people by leveraging talent, diverse perspectives, and ambitious ideas. To learn more about Medtronic's business, mission, and commitment to diversity, please visit their website.,

You will be responsible for writing, supporting, and managing projects to create high-quality medical and scientific communications, such as literature reviews, abstracts, posters, slide sets, and complex manuscripts for publication or presentation at congresses or to internal medical and clinical teams. You will work from various data sources, including clinical study reports and patient profiles, to prepare these deliverables. Additionally, you will perform quality control checks and proofreading to ensure the final outputs meet customer expectations. You will manage multiple projects simultaneously, focusing on up to two brands at a time. Gathering feedback from customers and implementing customer management tactics will be an essential part of your role. You will also adhere to project management tools, standards, policies, and initiatives set by the organization. Following Novartis specifications for documentation, including Novstyle and templates, is crucial, as is tracking clinical trial milestones for assigned projects. Keeping records for all projects, including archiving, and ensuring audit, SOP, and training compliance are key responsibilities. You will be expected to train new colleagues when necessary and take on additional tasks as assigned. To qualify for this role, you should have a minimum of a Science degree or equivalent, with 8 years of Clinical Research (CR) experience for B.Sc. or equivalent, or 6 years of CR experience for M.Sc./M.Pharm. Desired qualifications include a Doctoral Degree or Qualification in Medical Sciences (MBBS/MD/equivalent), or a PhD with 4 years of CR experience, MBBS/equivalent with 4 years of CR experience, or MD with 2 years of CR experience. Novartis is committed to creating an inclusive work environment and diverse teams that reflect the patients and communities served. Joining Novartis means being part of a mission to reimagine medicine and improve lives. To learn more about Novartis and explore career opportunities, visit: https://www.novartis.com/about/strategy/people-and-culture For information on benefits and rewards offered at Novartis, refer to the Novartis Life Handbook: https://www.novartis.com/careers/benefits-rewards. If you are interested in staying connected and learning about future career opportunities at Novartis, join the Novartis Network here: https://talentnetwork.novartis.com/network.,

Role & responsibilities Good knowledge About process research, ROS, synthetic chemistry To assist in literature, search for experimentation, and finding suitable reagents, and methods Maintaining lab records, and preparing proper as per GLP documentation. Housekeeping maintenance of Lab & specific hood To synthesize the impurities as per requirements in scheduled time period Process optimization, validation and assist demonstration of the process in plant for commercialization Performing experiments, analysing the results, and come up with simple and scalable process

Key Responsibilities: Academic Mentoring Provide doubt-clearing sessions to address student queries related to their coursework. Assist students in exam preparation by clarifying core concepts. Grade student assignments and tests, helping them improve research and writing skills. Evaluate student progress and offer regular feedback for improvement. Online Tutoring Deliver online tutoring sessions for international university students across various subjects. Conduct individual or group tutorials in a virtual learning environment (VLE). Develop and present video lectures on specialized academic topics. Academic Research Assistance Guide students on research methods and analysis to help them complete their research papers. Proofread and review students research papers, offering guidance on enhancements. Develop sample research papers for students to use as references when completing assignments. Core Responsibilities: Assess students individual learning needs and customize mentorship accordingly. Understand the learning objectives of academic programs, including research methodologies, referencing styles, and grading criteria. Conduct secondary research and demonstrate an in-depth understanding of academic concepts. Prepare plagiarism-free academic papers with strong language and research competency. Collaborate effectively with internal teams to ensure smooth academic operations. Required Candidate profile: Excellent oral and written communication skills in English. Strong subject matter expertise in the chosen academic field. Advanced research and analytical skills. Passion for academic research and writing. Willingness to learn and adapt to new subject areas and skill sets. Qualifications: We are looking for candidates from the following domains with respective qualifications: Management: MBA (Finance, HRM, Operations Project Management) Public Health / Hospital Administration / Pharmaceutical Management Law: LLB / LLM Nursing/Medicine: M.Sc. in Nursing / BDS / MDS / MBBS Accounting Finance: CA / CFA / B.Com / M.Com Economics: M.Sc. / Ph.D. in Economics Statistics: M.Sc. in Statistics Engineering (All Branches): B.Tech / M.Tech

RRD GO Creative is seeking experienced Medical Writers to join our team in Chennai. In this role, you will play a crucial part in developing high-quality and scientifically accurate medical and regulatory documents, such as clinical study reports, protocols, and brochures. Your responsibilities will also include creating clear and concise medical content tailored for healthcare professionals, regulatory agencies, and internal stakeholders. To excel in this role, you must conduct thorough research and literature reviews to ensure content accuracy and compliance with industry standards. Collaborating with subject matter experts, scientists, and regulatory teams is essential to develop compelling and compliant medical writing materials. You will be expected to adhere to client and regulatory guidelines, such as ICH, FDA, and EMA, while ensuring consistency, accuracy, and scientific integrity in all documents. As a Medical Writer, you will review and revise content based on feedback from reviewers and editors, manage multiple writing projects simultaneously while meeting strict deadlines and quality standards, and support quality control and peer-review processes to ensure excellence in medical documentation. Requirements for this role include a Bachelor's, Master's, or Doctorate degree in Life Sciences, Medicine, Pharmacy, or a related field, along with at least 3 years of experience in medical writing within the pharmaceutical, healthcare, or life sciences industries. A strong understanding of medical and scientific terminology, clinical research processes, and regulatory requirements is crucial. Additionally, excellent writing, editing, and verbal communication skills are necessary, with an eye for detail. Experience in preparing clinical and regulatory documents, publications, and scientific communications is preferred. You should be able to interpret and summarize complex scientific data for different audiences and possess familiarity with industry guidelines such as ICH, GCP, AMA, FDA, and EMA. Proficiency in Microsoft Office Suite and reference management tools is required, along with strong organizational skills, multitasking abilities, and the capacity to work independently under tight deadlines. Moreover, experience collaborating with cross-functional teams, including researchers, medical professionals, and regulatory experts, will be beneficial in this role. Join RRD GO CreativeTM, a company with over three decades of experience in business communications, marketing solutions, and digital productivity solutions. Our expertise in Global Brand Solutions, Smart Work Solutions, and Technology & Innovation Services enables us to transform the way businesses interact with customers, fostering strong brand loyalty. Our team of 8,000 experts across 42 locations collaborates across various industries to co-create a future-ready business landscape. We work with businesses to digitize every aspect of the Customer Journey, translating strategic visions of expansion and efficiency into superior Customer Experiences. Let us help you address customer needs effectively and make Customer Experience your competitive differentiator.,

About us Royal Pharma is a trusted pharmaceutical company based in Mumbai. With over 15 years of experience, we specialize in advanced intermediate and API manufacturing. Our facility is USFDA Approved and holds WHO GMP Certification, ensuring the highest standards of quality, safety, and efficacy. We are also ISO 9001:2015, ISO 14001:2015, ISO 45001:2018 certified. Collaborating with top multinational companies, we have expanded our reach worldwide, with a focus on delivering trusted healthcare solutions that have a positive impact on individuals' lives. Position Summary : A research and development (R&D) chemist uses their knowledge of chemistry and chemical engineering to create and improve products and processes. They have to Use chemistry and chemical engineering to develop new products, processes, and technologies. For improving existing products and processes they have to do Test and evaluate same. They have to Plan and run projects. Location: Boisar Years of Experience : Min 3 to Max 12 ( Please note only Male candidate will be suitable for this pos t , No Female candidate will be considered for opening) Key Responsibilities: 1. Project Handling, Optimization, Development. 2. Improving Existing Product to meet Customer Need. 3. To Prepare Product costing based on raw materials and manufacturing costs. 4. To conduct continual testing, improvement and scaling of new and existing Product. 5. Perform the Experiment. 6. Interpretation of analytical data, HPLC, GC, Mass. 7. Maintain the Safety & Following the safety Norms. 8. Provide suggestion regarding the present Experiment 9. Writing note book with all observations. 10. Capable to handle team members 5 to 6 11. Knowledge of literature search 12. Daily update about work and further planning Industry Pharmaceutical Manufacturing Employment Type Full-time If interested then please share your updated profiles on anaghasawant@royalpharma.in or sonampawar@royalpharma.in

The job involves preparing literature review, abstracts, posters, slide sets, and manuscripts from various data sources such as clinical study reports and patient profiles. Quality control and proofreading of deliverables are essential to meet customer expectations. Adherence to project management tools, standards, policies, and initiatives is required. Record-keeping for projects and compliance with auditing, SOP, and training are key responsibilities. The role is for a Consultant / Sr. Consultant - Scientific Writer in the Pharmaceutical industry. It is a full-time, permanent position in the outsourcing/Offshoring category. The key skills include literature review, abstracts, posters, slide sets, and manuscripts. Job Code: GO/JC/21340/2025 Recruiter Name: Mithra D,

PODDAR GROUP OF INSTITUTIONS is looking for Research Assistant to join our dynamic team and embark on a rewarding career journey Conduct Research:Plan and execute research projects in accordance with the organization's needs Utilize various research methods, including surveys, interviews, literature reviews, and data analysis Collect, compile, and analyze data to identify trends, patterns, and insights Data Collection and Analysis:Gather data from primary and secondary sources Employ statistical tools and software to analyze data and generate meaningful reports Interpret research findings and draw actionable conclusions Market Analysis:Monitor industry trends, competitor activities, and market dynamics Provide insights on market opportunities and threats to the organization Assess customer preferences and behavior Report Generation:Prepare detailed research reports and presentations Communicate research findings to relevant stakeholders Ensure that reports are clear, concise, and actionable Collaboration:Work closely with cross-functional teams, including marketing, product development, and management Collaborate with colleagues to share insights and align research efforts with organizational goals Project Management:Manage research projects, including timelines, budgets, and resources Ensure that research projects are completed on schedule and within budget constraints

RESPONSIBILITIES Book-in, Data Entry and Quality Reviewer of ICSR in Argus database ICSR Global Submission (Timelines and Submission Process) Vendor Management SOP training in department as and when needed DESIRED SKILLS Good knowledge about GVP (Good Pharmacovigilance Practices) modules and guidelines. Good knowledge about timelines and submission process of Global ICSRs w.r.t to multiple health authorities. Good knowledge about Global submission mailbox, maintenance of submission data and trackers of all ICSR submission activities including correspondence with regulatory authorities and submission records for audits and inspection readiness. Basic knowledge of Computers Good Communication skills

Job description - Research Associate (Protein Chemistry laboratory) 1. Process development, scale-up and transfer: (Downstream) Undertake on-going referencing and literature reviews and provide strategic inputs to projects at all stages Conduct lab experiments as per the shortlisted methodologies in order to develop & finalize purification processes for various recombinant therapeutic products. Provide own inputs and insights to optimize/improve process Provide samples to analytical labs for testing, collect and file reports of analysis, compile the data and do data analysis for conclusion of experiments Support plant activities as per need Present data in project review meetings Prepare process development report and technology transfer documents Participate in at-scale demo batches and handover as part of technology transfer Jointly monitor purification process at production facility and resolve any queries that may arise during production 2. Materials and equipment management: Oversee installation of new equipment and attend demos Maintain all IQ/OQ/PQ documents Ensure scheduled and breakdown maintenance by coordinating with maintenance team Create and maintain all maintenance/ repair logs Support management of chemical, consumables: o Transfer/store as per set norms o Engage in technical discussions with vendors in order to suggest suitable vendors o Maintain material logs and calculate shortfalls (for order placement) o Post materials required onto SAP 3. Regulatory and compliance: Accurately capture all lab experiments in laboratory notebooks in real-time Adhere to regulatory, SOPs and safety guidelines for all processes Modify SOPs in own area of work Ensure timely closure of regulatory queries by conducting and documenting lab experiments Ensure data integrity in all respects 4. Learning and improvement Attend all mandatory trainings Take initiative to provide inputs (based on expertise/interest) to other on-going projects Take initiatives for self-development and update self on recent developments in own area of work Take initiative to train fresh RAs upon induction or guide them with select lab processes (basis expertise) 5. Compliance management Ensuring GDP compliance Ensuring CC/ IQ/OQ/PQ/CSV of new instrument Ensuring calibration/PM/AMC of equipment Be audit ready and prepare audit responses as per audit points Lab cleanliness, lab maintenance