286 Scientific Writing Jobs - Page 12

We are looking for a highly motivated and detail-oriented individual to join our team as a Trainee Medical Reviewer in Bengaluru. The ideal candidate should have 0-1 years of experience. Roles and Responsibility Conduct thorough medical reviews of patient records and reports to ensure accuracy and compliance with regulatory requirements. Collaborate with cross-functional teams to identify and resolve issues related to medical review. Develop and maintain expertise in medical terminology, regulations, and guidelines. Provide high-quality support to internal stakeholders through effective communication and documentation. Stay updated with changes in regulations and guidelines affecting medical...

Job Title: Medical Reviewer Human Anatomy Specialist About the Role: We are looking for a medically educated professional with a strong foundation in human anatomy to join our team as a Medical Reviewer . The ideal candidate will have 2-3 years of experience in medical research, teaching, or content review , and will be responsible for ensuring the clinical and anatomical accuracy of the medical visual content we create. This role also involves direct communication with clients to gather requirements, provide expert input, and discuss feedback. Key Responsibilities: Review medical illustrations and other visual content for accuracy and consistency. Provide expert guidance to creative teams d...

Job Purpose To proactively develop journals in order to deliver growth in terms of published content. To build relationships with authors and editors such that journals meet or exceed their published content targets. Key Accountabilities Manage peer review processes, up to and including recommendations, within agreed timeframes, as required; ensure that all published content meets required ethical and scientific standards; recommend changes to peer review processes to improve efficiency. Support internal and external stakeholders to ensure that journals publish high quality content consistently and in a timely manner. Undertake to maintain strong subject knowledge within allocated journal fi...

Preparation and review of aggregate reports such as Periodic Benefit-Risk Evaluation Reports (PBRERs), Periodic Adverse Drug Experience Reports (PADERs), Risk Management Plans (RMPs), Addendum to Clinical Overview (ADCO) etc Co-ordination with various stakeholders to gather data required for Aggregate reports Work closely with service providers and resolve their queries Co-ordinate with various stakeholders internal and external required for the completion reports Preparation and review of Query responses from Regulatory Authority

Hands on experience in Clinical Research studies

Responsibilities: Leading evidence synthesis standalone projects and workstreams on broader engagements, as the person responsible for overall quality, timelines, and financial performance Developing recommendations based on expected impact, communicating risks and opportunities to ensure staff alignment, and where appropriate assuming the role of final decision maker Reviewing and signing off on deliverables including protocols, analysis plans, technical reports, and slides Work closely with ZS client teams to lead client business development and client relationship development across our key client accounts; Owning relationships with clients and being viewed as subject matter expert; proac...

Role Regional Managing Partner - Deputy Vice President, Kotak Agency - Field Sales (L7) Experience 6-12yrs. Job Role Recruitment Parameters -Increasing Distribution through Coding of new Partners & increasing LA base -Pragati Promotion -SAP / CAP Creation -Partner Promotion -Handhold & Coach Distribution for Recruitment -Minimum Distribution Criteria of 8:80 Business Parameters -Meet the budgeted business numbers -Maintain minimum Persistency of 85% -Coach & Train Agency to work Independently & Digitally -Meet the CLA numbers -Initiatives to improve Partner Income -Periodic meeting of Partners & Las -Support Agency with all relevant report & MIS Primary Responsibilities External Relations In...

Perform triage & intake of ICSR received daily in ARGUS databases Should have hands On Experience On ARGUS Safety Database Should Have hands on Experience on MEDDRA Applicants Should Complete Certification in Pharmacoviiglance Required Candidate profile B.Pharm / M.Pharm/Pharm D/Life sciences degree With Hands On Experience On Argus Safety Database and Med DRA coding, Argus, Narrative Writing, Triage

Role & responsibilities: 1. Support the scientific communication lifecyclefrom needs assessment through planning, writing, peer review, and submission/presentation. 2. Develop and maintain internal reports and evidence dossiers that summarize the performance and safety of products and technologies, incorporating relevant statistical findings and visualizations. 3. Provide data-driven support for scientific messaging by conducting literature searches, analyzing and summarizing experimental, analytical, or clinical datasets using descriptive and inferential statistics. 4. Interpret experimental and clinical data through collaboration with statisticians and technical experts to support accurate...

We are seeking a highly motivated and detail-oriented Research Analyst with 2+ years of experience in a research-related role, ideally in the life sciences, healthcare, or pharmaceutical sectors. The ideal candidate will have a strong foundation in conducting literature reviews, including systematic literature reviews, and preparing dossiers such as Global Value Dossiers (GVD) and Academy of Managed Care Pharmacy (AMCP) dossiers. This role will provide the opportunity to gain hands-on experience in supporting key research initiatives that influence strategic decision-making in the healthcare and pharmaceutical sectors. As a key member of our team, the candidate will support flexible working ...

Effectively collect and evaluate data, information, and input from multiple sources, functions, and regions to create a cohesive content strategy for writing projects. Plan (including organizing/preparing outlines), write (including first-draft authoring), edit, review, coordinate, and complete the regulatory documents supporting clinical development/product registration. Conduct effective document initiation meeting to ensure authoring team alignment and understanding. Build scientific-based rationale that support the purpose of more complex and/or strategic documents. Ensure data are presented in a clear, complete, accurate, and concise manner. Ensure that key data, statements and conclusi...