7 Evidence Synthesis Jobs

As a Technical Lead for TB Programs, you will play a crucial role in enhancing TB prevention, diagnosis, and treatment services. Your responsibilities will include providing strategic guidance, operational direction, and technical expertise to strengthen TB services. You will focus on enhancing coverage of Tuberculosis Preventive Therapy (TPT), collaborating with medical colleges, implementing innovative TB care approaches, and effectively managing Drug-Resistant TB (DR-TB). Your collaboration with the Deputy Director TB programs and partner agencies will involve synthesizing evidence to identify gaps in TB care coverage, ensuring efficient project execution, conducting capacity building ini...

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 ...

In this role at ZS, as an Evidence Synthesis Lead within the Health Economics and Outcomes Research (HEOR) team, you will play a crucial part in elevating HEOR into a strategic function that bridges the scientific, clinical, and commercial spheres. Your main responsibility will be leading evidence synthesis standalone projects and workstreams on broader engagements, ensuring overall quality, timelines, and financial performance. You will also be involved in developing recommendations, reviewing deliverables, and leading client business development efforts. Additionally, you will play a key role in team development, mentoring, and contributing to long-term strategic planning. **Responsibiliti...

As an Associate Director, Data Sciences at Certara, you will play a crucial role in leading the development, quality assurance, and delivery of clinical trial outcome databases across various therapeutic areas. Your responsibilities will include: - Overseeing database development, curation, QC, and deployment to the platform (e.g., CODEX). - Ensuring accurate data extraction from literature and plots, validating QC documentation, and managing change impact. - Conducting systematic literature reviews using PICOS, ontologies, and data standards, refining search strategies, and applying clinical trial knowledge. - Performing R-based quality checks and exploratory analyses. - Leading planning an...

As a member of the Global Health Economics & Outcomes Research (HEOR) team at our company, your role will involve developing and updating Global Value Dossiers (GVDs), US AMCP dossiers, EU JCA dossiers, and early HTA briefing books across multiple therapeutic areas. You will also contribute to HEOR publication execution by developing abstracts, posters, and manuscripts while assisting in the creation of training materials and onboarding documents for HEOR writing resources. It is essential for you to adhere to internal processes and ensure compliance with publication and HTA standards. Key Responsibilities: - Develop and update Global Value Dossiers (GVDs), US AMCP dossiers, EU JCA dossiers,...

As a Global HEOR Value Writing Senior Associate in the Global Health Economics & Outcomes Research (HEOR) department, your role involves developing and updating Global Value Dossiers (GVDs), US AMCP dossiers, EU JCA dossiers, and early HTA briefing books across multiple therapeutic areas as assigned by the team lead. You will also contribute to HEOR publication execution by developing abstracts, posters, and manuscripts. Additionally, you will assist in creating training materials and onboarding documents for HEOR writing resources. It is essential to adhere to internal processes and ensure compliance with publication and HTA standards. You will be responsible for reviewing and QC work of pe...

ZS is a place where passion changes lives. As a management consulting and technology firm focused on improving life and how we live it, our most valuable asset is our people. Here you'll work side-by-side with a powerful collective of thinkers and experts shaping life-changing solutions for patients, caregivers, and consumers, worldwide. ZSers drive impact by bringing a client-first mentality to each and every engagement. We partner collaboratively with our clients to develop custom solutions and technology products that create value and deliver company results across critical areas of their business. Bring your curiosity for learning; bold ideas; courage and passion to drive life-changing i...