131 Literature Review Jobs - Page 2

Concept Pharmaceuticals Ltd. 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 i...

As an Epidemiologist, you are responsible for conducting analytical research to support the needs of customers including performing fully documented systematic reviews of both published and grey literature on the epidemiology of assigned diseases and their risk factors to estimate incidence/prevalence over a 1020-year period. Conduct research using online grey literature datasets such as NHANES, HCUP, cancer registries, government survey data, and other resources to summarize current information on prevalence, and to forecast numbers for a variety of diseases; and suggest use of proxy data sources or develop imputation or extrapolation models when country-specific sources are not available. ...

As an Epidemiologist, you are responsible for conducting analytical research to support the needs of customers including performing fully documented systematic reviews of both published and grey literature on the epidemiology of assigned diseases and their risk factors to estimate incidence/prevalence over a 1020-year period. Conduct research using online grey literature datasets such as NHANES, HCUP, cancer registries, government survey data, and other resources to summarize current information on prevalence, and to forecast numbers for a variety of diseases; and suggest use of proxy data sources or develop imputation or extrapolation models when country-specific sources are not available. ...

As a Junior Research Fellow (JRF) at Amity Institute of Click Chemistry Research and Studies, you will be involved in a time-bound research project focused on the synthesis of Halogenated and Chalcogenated Porphyrins for Catalysis Reaction, specifically exploring the Role of Halogen Bond (XB) and Chalcogen Bond (CB) Interactions. Key Responsibilities: - Conduct research activities related to the synthesis of organic and inorganic materials for catalysis reactions - Collaborate with the research team to analyze and interpret experimental results - Assist in the documentation of research findings and preparation of reports - Stay updated with relevant literature and advancements in the field o...

As a Consultant / Sr. Consultant - Scientific Writer, your role 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 are responsible for performing quality control (QC) checks and proofreading of the deliverables to ensure they meet customer expectations. It is essential for you 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. - Prepare literature reviews, a...

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life The Clinical Evaluation Medical Writer on our Endoscopy team plays a key role in developing and updating clinical evaluation documents (e.g., CEP, CER, PMCFP, PMCFR, SSCP) to support CE Mark submissions and maintain compliance throughout the product lifecycle. This work follows MEDDEV 2.7/1 Rev. 4 and EU Regulation 2017/745 and involves close collaboration with cross-functional teams to gather and interpret data on device safety, perfo...

Reports To: Global Systematic Literature Review Team Lead Position Summary The Global Systematic Literature Review (SLR) Senior Associate provides expertise in designing, executing, and managing literature review services within Amgens Global HEOR function. The SLR Senior Associate will collaborate closely with team lead and Global HEOR Product Leads to align with HEOR product strategy. This role supports global access to Amgen's therapies through the generation of high-quality, evidence-based outputs across the product lifecycle. Key Responsibilities Refine literature review questions in alignment with team lead and prepare research protocols. Design literature searches for electronic datab...

What you will do The Global HEOR Systematic Literature Review (SLR) Leader oversees the development and delivery of systematic literature review activities within Amgens Global HEOR function. This operational and managerial role includes supervision of a team of Global HEOR SLR Analysts, ensuring high-quality, timely, and scientifically robust literature review outputs. The Global HEOR SLR Leader will align closely with Global HEOR TA Heads in support of global market access and value demonstration for Amgens products across their lifecycle. Lead, mentor, and handle a team of Global HEOR SLR Analysts, fostering a high-performance culture. Oversee the design, execution, and quality control of...

Do you want an exciting position working with multiple teams to generate real world evidence supporting a wide variety of business needs Amgen focuses on areas of high unmet medical need and leverages its expertise to strive for solutions that improve health outcomes and dramatically improve peoples lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the worlds leading independent biotechnology companies, has reached millions of patients around the world, and is developing a pipeline of medicines with breakaway potential. Observational research (OR) is an increasingly important component in drug development and commercialization. There is increased demand for information ...

Role & responsibilities 1. Works closely with cross-functional project teams to independently author scientifically accurate, comprehensive and compliant documents, including but not limited to clinical study reports, clinical study protocols, manuscripts, informed consent forms, patients' narratives, abstracts, posters, oral presentations, etc. 2. Manages the collection, consolidation and integration of comments/feedback from internal and external reviewers to efficiently finalize assigned writing projects 3. Performs thorough quality control checks, including copyediting, proofreading, and cross-verification of data within clinical documents and against source TFLs to ensure accuracy, cons...

As a Junior Research Fellow at the National Institute of Technology Rourkela, your primary responsibility will be to work on the project (CAMP) under the Centre for Mahanadi River Basin Management studies. This full-time on-site role includes conducting research, data analysis, literature reviews, and supporting senior researchers in various projects based in Rourkela. Key Responsibilities: - Work on the project (CAMP) under the guidance of the Coordinator and PIs. - Conduct research, data analysis, and literature reviews. - Assist senior researchers in project activities. Qualifications Required: - Hold an M.Sc. in Life Science / Env. Sci/ Ecology/ Biodiversity/ Microbiology / Zoology/Biote...

Roles and Responsibilities Candidate will be required to do desk research on various domains like Management, Commerce, Social Science 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 MBA, MSc or M.A in English, Mass Communication, Political Science, Law, with excellent English writing skills. Desk research and ability to understand basics of statistical analysis will be an added advantage. Perks and Ben...

Roles and Responsibilities Develop new APIs through organic synthesis, method development, and optimization. Conduct literature reviews to stay updated on latest research trends and technologies. Ensure compliance with GMP guidelines during API manufacturing processes. Collaborate with cross-functional teams for product development, scale-up, and commercialization. Perform impurity analysis using techniques like NMR, DSC, etc. Desired Candidate Profile MS/M.Sc(Science) degree in Chemistry or Ph.D/Doctorate in Chemical Sciences from a recognized university. Strong expertise in areas such as API synthesis, organic chemistry, method development/validation/transfer/methodology. 9-14 years of exp...

Summary In close collaboration with the Global Program Safety Lead (GPSL) provides robust safety evaluation expertise and medical innovation in order to improve patients lives and impact on overall Novartis results. Ensures optimal patient safety for assigned compounds by identifying new safety signals early using internal and external spontaneous reporting databases. About The Role Major accountabilities: Lead the safety signal detection and triage activities for a challenging product portfolio. Identify new safety signals early based on review and comprehensive medical evaluation of technical hits in postmarketing spontaneous reporting databases analyzing single case reports as well as agg...

As a Safety Signal Detection Lead at Novartis, your primary responsibility will be to lead the safety signal detection and triage activities for a challenging product portfolio. You will play a crucial role in identifying new safety signals early by reviewing and comprehensively evaluating technical hits in postmarketing spontaneous reporting databases. Your expertise will be required to provide expert evaluation of postmarketing signal detection activities at cross-functional team meetings and collaborate effectively with safety leads and cross-functional teams. Key Responsibilities: - Lead safety signal detection and triage activities for the product portfolio - Identify new safety signals...

Profile Summary The main goal of this role is in contributing to our organization's growth by conducting comprehensive research, writing research articles across various fields, and managing the publication process. Key Roles and Responsibilities Research Article Writing: Conduct in-depth research across diverse fields and produce high quality research articles for publication. Collaborate with subject matter experts to ensure accuracy and relevance in content. Publication Strategy: Demonstrate expertise in the research publication process, including selecting appropriate journals, understanding submission guidelines, and ensuring compliance with publication standards. Submission Follow-up: ...

Assist the Principal Investigator in fieldwork, data collection, and analysis. Draft, refine, and administer research tools such as questionnaires and interview schedules. Conduct literature review and support preparation of research reports. Coordinate with participants, stakeholders, and institutions relevant to the project. Assist in documentation, progress reports, and dissemination of project findings.

proofreading Job Title: Evidence Synthesis & Medical Writing Job Location: - Gurgaon/Noida (Hybrid) 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 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 ...

Roles and Responsibilities JD for Regulatory services Scientific web research to collect information related to health and environmental hazard of substances present in the chemical products. Review of Scientific articles. Interpretation of data from literature by referring international guidance. Study report preparation with the literature findings Preparing globally compliant document for supply chain communication. SDS Authoring and updating the Safety Data Sheets (SDS) with regulatory requirements Skilled in regulatory compliance and chemical safety, Lisam exess , 1907/ 2006 regulations, product stewardship etc JD for Scientific research Scientific web research to collect information re...

Summary In close collaboration with the Global Program Safety Lead (GPSL) provides robust safety evaluation expertise and medical innovation in order to improve patients lives and impact on overall Novartis results. As a member of the Medical Safety organization, prioritizes the safety of patients, ensures optimal patient safety for assigned compounds and shares responsibility for the integration, analysis, and evaluation of internal and external safety information through product lifecycle management, and evaluation of internal and external safety information through product lifecycle management About The Role Key Responsibilities Monitors the clinical safety of projects/products including ...

Role Overview: As a Clinical Safety Scientist - Lead, your primary responsibility will be to conduct literature reviews to assess ICSR and new safety signals for inclusion in Aggregate reports and DSR (Drug Safety reports). You will also provide MAH comments for selected literature and review Literature Strategy. Additionally, you will be involved in designing and interpreting various types of studies in medicine, assessing levels of evidence, study power for safety analyses, and reviewing outputs triaged by safety scientists for scientific accuracy based on specific criteria. Moreover, you will be responsible for authoring Safety Sections of SSSRs, DSUR, aCO, PBRER, RMP updates, and impleme...

Hiring for Clinical Safety Physician in Mumbai, Bangalore & Noida Any MBBS/MD with min 5 yrs of relevant Exp in Drug Safety, ICSR, Aggregate reporting, Clinical Study Salary up to 25 LPA Call Suhani- 9911988552, Rukhsar-9899875055, Shruti-9911988551

Role & responsibilities Responsible for literature search and designing ROS, POC of assigned projects Responsible for the development of plant feasible process, process development and delivering PLP, LDR as an output for smooth technology transfer to plant for Piloting and commercial production. Perform the reactions on small as well as large scale in the lab for the synthesis of target compounds Purification of compounds through various techniques such as crystallization, column chromatography, and advanced flash purification systems. Expertise in characterization of organic compounds using spectroscopic techniques• H, C NMR, LCMS, IR. Generation of process data like what-if study, process...

Role & responsibilities Responsible for literature search and designing ROS, POC of assigned projects Responsible for the development of plant feasible process, process development and delivering PLP, LDR as an output for smooth technology transfer to plant for Piloting and commercial production. Perform the reactions on small as well as large scale in the lab for the synthesis of target compounds Purification of compounds through various techniques such as crystallization, column chromatography, and advanced flash purification systems. Expertise in characterization of organic compounds using spectroscopic techniques• H, C NMR, LCMS, IR. Generation of process data like what-if study, 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