3 Data Abstraction Jobs

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 systematic literature reviews across therapeutic areas. Supervise the development of research protocols, screening strategies, and data abstraction tools. Collaborate with HEOR TA Heads to align literature review outputs with HEOR strategy. Serve as the functional guide on literature review within HEOR. Ensure consistency with PRISMA, PICOS, and other industry standards for evidence synthesis. Support integration of SLRs into HTA submissions, global value dossiers, and peer-reviewed publications. Continuously improve workflows, tools, and methodologies to enhance review efficiency and quality. Contribute to hiring, training, and performance evaluations within the SLR team. What we expect of you We are all different, yet we all use our unique contributions to serve patients. The HEOR Systematic Literature Review Leader we seek should possess these qualifications. Basic Qualifications & Experience: Doctorate degree in health economics, public health, Epidemiology, Pharmacy, life sciences or related field and 2 years of experience in systematic literature reviews and evidence synthesis in the pharmaceutical, biotech or consulting setting OR, Masters degree in Health Economics, Public Health, Epidemiology, Pharmacy, life sciences or related field and 8 to 10 years of experience in systematic literature reviews and evidence synthesis in the pharmaceutical, biotech or consulting setting OR, Bachelors degree in Health Economics, Public Health, Epidemiology, Pharmacy, life sciences or related field and 10 to 14 years of experience in systematic literature reviews and evidence synthesis in the pharmaceutical, biotech or consulting setting OR, Diploma in Health Economics, Public Health, Epidemiology, Pharmacy, life sciences or related field and 14 to 18 years of experience in systematic literature reviews and evidence synthesis in the pharmaceutical, biotech or consulting setting 3+ years of experience in team management capacity. Skills & Competencies: Exceptional leadership, mentoring, and project management skills. Excellent English oral and written communication, with ability to tailor content to different key partners; past medical writing experience is a plus Advanced proficiency with systematic review tools and citation databases (e.g., PubMed, EMBASE). Skilled in Microsoft Office (Word, PowerPoint, Excel); experience with EndNote or other reference tools preferred. High attention to detail, quality assurance, and evidence integrity. Innovative use of artificial intelligence to boost efficiency Organizational Behaviors: Solution-oriented with a continuous improvement attitude. Strong interpersonal and customer engagement capabilities. Comfortable working in a distributed team across time zones and cultures.

Part of the Oncology Clinical Team, working on building Oncology Data dictionaries, Curation/Abstraction SOPs etc. Position Summary: The Person navigates electronic medical record systems and other medical databases. This role involves reviewing clinical trial data for consistency, completeness, and compliance with study protocols and regulatory requirements. reviews medical records, and abstracts medical record data related to specified disease and project requirements. Essential Job Functions: Screening of cases for relevant clinical trials across various projects and/or disease subtypes. Knowledge related to cancer trials is essential and required, including understanding their inclusion and exclusion criteria. Ability to use critical thinking to understand and abstract complex concepts. Building of data libraries and liaising with multiple departments when project specific requirements/needs arise. Act as an oncology subject matter expert (SME) across all cancers, especially across liquid cancer types. Access electronic data systems for review of medical records and enter specific data into congruent electronic data systems. Ability to understand the Inclusion, Exclusion criteria, adverse event, hospitalization data, medications details and categorize the data accordingly. Review project specific documents, as needed, to develop familiarity with project goals and with the Abstractor tasks in each project. Ability to understand the diagnostic, pathology and other reports and obtain the exact information required according to trial specific SOPs. Use other resources as needed to gain the knowledge required to perform Abstractor work on new projects. Share medical knowledge and project-specific procedural knowledge with other Data Abstractors as needed. Respond promptly to queries issued by the Lead Data Abstractor, Operations Manager or other project personnel. Conduct additional duties as assigned, including review of selected medical records to assess eligibility for new project, performing second level reviews/QC review of medical records. Qualification: Minimum 3+ years experience across data abstraction or any patient treatment related data is desirable. Oncology experience is preferable; familiarity with how cancer is treated from diagnosis through treatment and recovery and an understanding of cancer terminology, with a strong focus and knowledge on liquid tumors is essential. Experience in clinical research or related fields, especially in oncology trials is preferred. An advanced level of clinical knowledge associated with chronic disease states is required. Experience in clinical research or reviewed medical data for clinical trials. Certification done in clinical research or clinical data management. Education: B.Sc (Nursing), BDS, BAMS, BHMS, MDS, BPharm, MPharm Skills and Abilities: Language: Strong communication skills both written and verbal to work with multiple internal and external clients in a fast paced environment. Reasoning: Ability to make independent judgments in abstracting medical data and the knowledge of when to seek input from other staff. Flexibility: Flexibility in coping with changing work assignments, changing project requirements, varying training meeting schedules, and database resources that may not always function optimally. Computer: Ability to create and maintain documents using Microsoft office( word, excel, outlook and powerpoint)"

Hello Everyone! Warm Greetings from Omega Healthcare! Were thrilled to share a fantastic opportunity for life science graduates looking to dive into the field of oncology. Position: Trainee Medical Reviewer ( Fresher only) Location: Bangalore (Onsite - Day Shift) Employment Type: Full-Time What You'll Do: Step into the role of an Oncology Trainee Medical Reviewer and make an impact! Youll be working hands-on with patient medical records, where your job will be to identify and abstract essential data points in line with specific guidelines. A good grasp of chemotherapy, oncology drugs, and medical oncology reports will be key as you summarize critical insights from your findings. Your Responsibilities: Dive into patient electronic medical records, reviewing and abstracting data based on the SOPs. Get up to speed on project goals, including what data is in or out, to keep your work spot on. Maintain the quality benchmarks for all the data you curate. Analyze diagnostics, procedures, treatments, and genetic tests from patient charts. Use your knowledge of oncology meds and treatments to interpret reports effectively. Who Were Looking For: Fresh graduates from Life Sciences, Dental, Nursing, Pharmacy, or Paramedical fields. Domain Focus: Abstracting clinical data from EHRs for oncology patients. Data points will vary with cancer type and may include genetic test results, line of therapy (LOT) for chemo drugs, clinical disease status, lab values, and more. Ready to Apply? Direct walk-in Interview Venue Details: Omega Healthcare - F2 Airport Bengaluru, Karnataka Rustam Bagh Layout, Bengaluru, Karnataka 560017 [Google Maps Location] Applicant has to get prepare on Oncology , Human anatomy & Genetic subject. Salary :- 2.5L Annually. Monthly TH - 15TH Looking forward to seeing you join our dynamic team! Best, Mohammed Mansoor