15 Literature Review Jobs

Supriya life science ltd is looking for Research Scientist - FRD (Injectable) to join our dynamic team and embark on a rewarding career journey. Research Planning : Develop and design research projects, experiments, and studies to investigate specific scientific questions or problems. Create detailed research plans, including methodologies, timelines, and resource requirements. Data Collection and Analysis : Perform experiments, gather data, and conduct data analysis using various scientific methods, statistical techniques, and specialized equipment. Interpret and evaluate the results to draw meaningful conclusions. Literature Review : Stay up - to - date with relevant scientific literature and research developments in the field. Analyze existing research to identify gaps and opportunities for further investigation. Hypothesis Testing : Formulate hypotheses and test them through experimentation. Analyze the outcomes to validate or invalidate the hypotheses. Innovation and Problem Solving : Utilize critical thinking and creativity to devise new approaches to scientific challenges. Propose and develop innovative solutions to complex problems. Collaboration : Collaborate with interdisciplinary teams, researchers, engineers, and other stakeholders to exchange knowledge, ideas, and expertise. Participate in discussions and contribute to group projects. Presentation and Communication : Present research findings to both technical and non - technical audiences through reports, presentations, scientific papers, and conferences. Effectively communicate complex scientific concepts in a clear and concise manner. Safety and Compliance : Adhere to safety protocols and ethical guidelines in conducting experiments and handling hazardous materials. Ensure compliance with all relevant regulations and institutional policies. Equipment Maintenance : Maintain and troubleshoot laboratory equipment to ensure accuracy and reliability in research activities.

The Research Analyst in PhD Assistance supports academic research by gathering and analyzing data, conducting literature reviews, and preparing reports. This role helps PhD candidates and faculty members by ensuring high-quality, evidence-based research work. Roles & Responsibilities: Literature Reviews & Data Collection: Conduct thorough literature reviews to gather relevant academic resources. Collect and organize research data from various sources. Data Analysis: Analyze quantitative and qualitative data using research tools and software. Summarize findings to support research projects. Report Preparation: Create detailed research reports, summaries, and presentations. Assist in preparing materials for academic publications and grant proposals. Research Support: Collaborate with PhD candidates and faculty to refine research methodologies. Provide technical assistance and guidance in research best practices. Database & Documentation Management: Maintain organized records and databases of research materials. Ensure all research processes meet academic standards and documentation practices.

KASHI INSTITUTE OF TECHNOLOGY is looking for Senior Research Assistant (SRA) / Research Assistant ( RA) to join our dynamic team and embark on a rewarding career journey Conduct Research: Design and execute experiments or research projects under the guidance of senior researchers or project leaders. Collect, analyze, and interpret data using various research methodologies and tools. Literature Review: Review relevant literature to understand the current state of knowledge in the research area. Stay updated on advancements in the field and incorporate relevant findings into ongoing research. Data Collection and Analysis: Utilize appropriate techniques to gather data, whether through experiments, surveys, interviews, or other methods. Analyze and interpret data using statistical methods or other relevant analytical approaches. Report Writing: Prepare detailed reports summarizing research findings, methodologies, and conclusions. Contribute to the writing of research papers, articles, and presentations for conferences or publications. Collaboration: Work closely with team members, senior researchers, and other stakeholders to achieve research goals. Participate in research meetings, seminars, and conferences. Equipment and Lab Maintenance: Maintain and operate laboratory equipment as needed. Ensure proper documentation and organization of research materials. Compliance and Ethics: Adhere to ethical guidelines and standards in research activities. Ensure compliance with relevant regulations and protocols.

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 & 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

Job Title: Evidence Synthesis & Medical Writing Job Location: - Gurgaon/Noida/Hyderabad Job Responsibilities: - Contribute to projects specific to Targeted literature reviews (TLR) / Systematic Literature reviews (SLR) / Value dossiers (GVD or AMCP) / Scientific publications (abstracts, posters, manuscripts) etc. Ensure to deliver at highest quality in stipulated timeliness Ensure data are presented in a clear, complete, accurate, and concise manner o Performs quality control (QC) checking / proof reading of assigned documents Excellent knowledge of systematic review methodology/HTAs submissions Experience of writing market access documents such as Academy of Managed Care Pharmacy (AMCP) dossiers and global value dossiers (GVD) Experience in the analysis and interpretation of data, including report writing, is essential Be accountable and responsible for assigned activities such as writing, reviewing, literature searches, project management etc. Support growth of the business through the development of strong client relationships Guide and mentor junior team members Qualification: - Masters degree, PharmD, PhD or equivalent in medicine / pharmacy 3-6 years of experience in HEOR and medical writing domains Knowledge of various reference management software (EndNote / Reference manager) Experience of conducting meta-analysis and network-meta-analyses (RevMan, STATA, R) Proficiency in Microsoft Word, Excel and PowerPoint Additional skills: - Understanding of economic evaluation techniques and basic health economic modelling (EM) knowledge o Understanding of real-world evidence (RWE) studies Understanding the market access environment and challenges globally o Excellent time management, project management and communication skills Interpreting data, writing reports, and making actionable recommendations Proactive approach to work, problem-solving aptitude and flexible to learn and adapt Primary research or conducting workshop with key opinion leaders (KOLs) Behavioural Attributes Ability to execute assigned tasks both independently and collaboratively with minimal supervision Proactiveness in identifying solutions to challenges Growth mindset demonstrated through intellectual curiosity, critical thinking, and a drive for collective business success Skills that give you an edge: - Strong analytical skills to solve and model complex business requirements are a plus. With life sciences or pharma background. Medical writing experience Meta-Analysis (RevMan, STATA, R) Gen AI/ML skills o Analytical thinking ability Time management skill We will provide (Employee Value Proposition) Offer an inclusive environment that encourages diverse perspectives and ideas Deliver challenging and unique opportunities to contribute to the success of a transforming organization Opportunity to work on technical challenges that may impact across geographies o Vast opportunities for self-development: online Axtria Institute, knowledge sharing opportunities globally, learning opportunities through external certifications o Sponsored Tech Talks & Hackathons o Possibility to relocate to any Axtria office for short and long-term projects o Benefit package: -Health benefits -Retirement benefits -Paid time off -Flexible Benefits -Hybrid /FT Office/Remote Behavioural Attributes Ability to execute assigned tasks both independently and collaboratively with minimal supervision Proactiveness in identifying solutions to challenges Growth mindset demonstrated through intellectual curiosity, critical thinking, and a drive for collective business success Skills that give you an edge: - Strong analytical skills to solve and model complex business requirements are a plus. With life sciences or pharma background. Medical writing experience Meta-Analysis (RevMan, STATA, R) Gen AI/ML skills Analytical thinking ability Time management skill We will provide (Employee Value Proposition) Offer an inclusive environment that encourages diverse perspectives and ideas Deliver challenging and unique opportunities to contribute to the success of a transforming organization Opportunity to work on technical challenges that may impact across geographies Vast opportunities for self-development: online Axtria Institute, knowledge sharing opportunities globally, learning opportunities through external certifications Sponsored Tech Talks & Hackathons Possibility to relocate to any Axtria office for short and long-term projects Benefit package: -Health benefits -Retirement benefits -Paid time off -Flexible Benefits -Hybrid /FT Office/Remote

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

Job Summary: As a Medicinal Chemist, you will play a pivotal role in the design, synthesis, and optimization of novel drug candidates. This role requires scientific expertise, problem-solving skills, and hands-on laboratory experience to drive drug discovery projects from hit identification to lead optimization and preclinical development. You will work closely with cross-functional teams to develop innovative therapeutics that address unmet medical needs. Responsibilities: Design and synthesize novel small molecules to target specific disease indications. Planning and implementation of novel approach to drug discovery and development independently or in collaboration. Apply Structure-Activity Relationships (SAR) and Structure-Property Relationships (SPR) to optimize potency, selectivity, and pharmacokinetic properties. Collaborate with computational chemists, biologists, and pharmacologists to design and prioritize new chemical entities for synthesis and biological evaluation. Perform literature searches and analyze scientific literature to identify and implement new synthetic methodologies and technologies. Contribute to the preparation of patent applications, technical reports, and scientific publications. Use computational models and simulations to predict the behavior of new drugs and to guide the design of new compounds. Stay updated with emerging trends in AI-driven drug discovery and medicinal chemistry innovations. Understand Structure Activity Relationships and Structure Property Relationships of various projects. Qualifications and Skills: Ph.D. in Organic Chemistry, or related field. 10-13 years of industry experience in Life Sciences, R&D, CRO, biotech, or pharmaceutical settings. Strong background in synthetic organic chemistry, medicinal chemistry, and chemical biology. Proficiency in modern synthetic methods, purification techniques, and analytical instrumentation (e.g., NMR, LC-MS, HPLC). Demonstrated success in lead optimization and preclinical drug discovery. Familiarity with pharmaceutical industry practices and regulatory frameworks. Knowledge of AI-driven drug discovery methodologies is an advantage. Excellent problem-solving skills, scientific creativity, and a passion for innovation. Strong communication and interpersonal skills, with the ability to collaborate in a multidisciplinary environment.

Commissum (Eurofins Cyber Security UK) is looking for Research Scientist to join our dynamic team and embark on a rewarding career journey. Research Planning: Develop and design research projects, experiments, and studies to investigate specific scientific questions or problems Create detailed research plans, including methodologies, timelines, and resource requirements Data Collection and Analysis: Perform experiments, gather data, and conduct data analysis using various scientific methods, statistical techniques, and specialized equipment Interpret and evaluate the results to draw meaningful conclusions Literature Review: Stay up-to-date with relevant scientific literature and research developments in the field Analyze existing research to identify gaps and opportunities for further investigation Hypothesis Testing: Formulate hypotheses and test them through experimentation Analyze the outcomes to validate or invalidate the hypotheses Innovation and Problem Solving: Utilize critical thinking and creativity to devise new approaches to scientific challenges Propose and develop innovative solutions to complex problems Collaboration: Collaborate with interdisciplinary teams, researchers, engineers, and other stakeholders to exchange knowledge, ideas, and expertise Participate in discussions and contribute to group projects Presentation and Communication: Present research findings to both technical and non-technical audiences through reports, presentations, scientific papers, and conferences Effectively communicate complex scientific concepts in a clear and concise manner Safety and Compliance: Adhere to safety protocols and ethical guidelines in conducting experiments and handling hazardous materials Ensure compliance with all relevant regulations and institutional policies Equipment Maintenance: Maintain and troubleshoot laboratory equipment to ensure accuracy and reliability in research activities

Job Responsibilities: A) Project Management Undertake on-going referencing and literature reviews and provide strategic inputs to projects at all stages Evaluate methods under consideration by conducting literature survey (incl. regulatory guidelines, pharmacopeia guidelines, publicly available research, etc.) Identify initial cell-lines/ anti-body requirement based on method(s) identified Conduct lab experiments for bio-assay/ immuno-assay development and optimization Conduct lab experiments to qualify the method for reproducibility Prepare/provide inputs for the preparation of necessary documents like Method development report, Method qualification protocol and report. Method validation protocol and report, Standard Analytical Procedures (SAP), Method transfer protocol and report. Ensure tech-transfer by demonstrating process to plant operators (in lab premises) Observe process in plant and resolve any queries that may arise (post-transfer) B) Bio-assay/Impurity assay (HCP and HCDNA) /Binding ELISA assay/SPR assay/BET Method development, qualification and transfer Conduct regular analysis for non-GMP and non- release batches (not transferred to plant) - support other labs by stability testing samples provided by them Prepare and share detailed reports with the relevant labs upon completion of the tests Conduct Bioassay, HCP, HCDNA, Protein A ELISA, SPR, Binding assay and BET method development/qualification and routine analysis (C) Other tests and routine processes Conduct / guide RAs for conduct of regular analysis for non-GMP and non-release batches (not transferred to plant) - Support other labs by stability testing samples provided by them tests as requested. Prepare/review and share detailed reports with the relevant labs upon completion of the tests Conduct/ guide RAs for conduct of method development/qualification and routine analysis Review protocols and reports provided by CRO (based on expertise) Coordinate CRO with ADA assays, Antibody generation, purification and biotinylating activity for in-house HCP method. (D) Materials and equipment management Procure and maintain inventory of cell-lines/anti-bodies/ consumables/ equipment: Share details of requirements with purchase team Engage in technical discussions with vendors to identify and recommend suitable ones to lab head and Supply Chain Raise PR for purchase Oversee Check materials upon receipt and store them as per set-norms (freeze in case of cell-lines) Track and maintain inventory in order to control and manage short-falls and damage Maintain inventory-logs and intimate superiors in case of short-falls and damage Manage cell-culturing and sub-culturing process: Prepare cell-banks (by freezing cell-lines) for storage Passage cells (remove vials from these banks) as per testing need Calibrate select lab-equipment on regular basis to facilitate use Ensure scheduled and break-down maintenance by coordinating with vendors/ maintenance team ( E) Regulatory and compliance Accurately capture all lab experiments in raw- data and lab-notebooks (incl. electronic data- capture) in real-time on an on-going basis. Adhere to regulatory, SOPs and safety guidelines for all processes. Ensure timely closure of regulatory queries by conducting and documenting lab experiments. Ensure data integrity in all respects Compile and Review all project-related documents created during lab activity on a regular basis Prepare/ modify SOPs by gauging work ability of the processes/practices in timely manner (F ) Business (people & budgets) planning, continuity and improvement Conduct SOP and induction trainings for subordinates Provide timely and relevant inputs for the preparation of capex budget Identify and implement continuous improvement initiatives to enhance process efficiency Take initiative to provide time and inputs (based on expertise/interest) to other on-going projects (G) 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) (F) Quality Compliance Initiate change control for New instrument IQ/OQ/PQ/CSV of new instrument. GDP Compliance Compliance related to internal and external audits

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 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. Qualifications : B.Sc / M.Sc (Organic Chemistry) Experience : Min 5-8 Years of Experience in the intermediates/API pharmaceutical industry

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

Innovative Research Services is looking for Research Executive 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

Design and execute experiments to develop and optimize robust and scalable manufacturing chemical processes of APIs Expert in organic synthesis and stay up to date with the latest scientific advancements and emerging technologies in the chemical process development Collect and analyze experimental data and generate clear and concise reports summarizing findings and recommendations Maintain accurate and detailed laboratory notebooks and electronic records in compliance with company policies and regulatory requirements. Prepare and review technical documents, including standard operating procedures (SOPs), batch records, and development reports. Collaborate closely with cross-functional teams, including research and development scientists, manufacturing personnel, and quality control, to ensure seamless technology transfer from process development to manufacturing Ability of planning, execution, and oversight of the technology transfer and validation of processes, ensuring the quality, safety, and efficacy of the product throughout the process. Leverage literature review and ongoing awareness of state of the art in designing and executing new routes Work effectively in a team environment to meet project objectives and timelines.

Role & responsibilities Literature review, feasibility evaluation and study design for Bioequivalence studies Thorough understanding of national and international regulatory guidance on Bioequivalence Review of clinical study documents of Bioequivalence studies in healthy subjects and patient PK study Clinical study monitoring Knowledge of IPs management Preparation and maintenance of Trial master file Oversee the overall management of Bioequivalence studies Basic understanding of project contract with service providers Ready to take up any other relevant tasks as and when needed