Clinical Data Management Specialist

Healthcare Operations Expertise: As a seasoned professional, you will leverage expertise in clinic operations, EHR/EMR systems, billing, coding, and healthcare data management to drive improved patient outcomes and enhanced operational efficiency.Key Responsibilities:Develop and implement streamlined clinic workflows that encompass front desk, clerical...

Job Overview:As a Clinical Data Management Specialist, you will be responsible for defining project specifications for data management services.Key Responsibilities:Define project specifications for data management services, including protocol conversion, database build, CRF design, and data review.Understand external data collection and its integration into...

Clinical Data Specialist Role The successful candidate will be responsible for creating and reviewing data specifications, developing analysis datasets, tables, listings, and figures. The individual must have a strong understanding of ICH-GCP guidelines, core operating procedures, and work instructions.

Data Review Associate Job OpportunityEmbark on a rewarding career as a Data Review Associate in our Global Clinical Coding Support team. This full-time, office-based role in Mumbai, India offers an exciting chance to specialize in clinical data review and development of guidelines for therapeutic areas.About the Role:Clinical Data Review: Manually review...

Job Summary:The Senior Manager of Clinical Research will lead and manage clinical trials and research studies, ensuring that they are completed on time, within budget, and in compliance with regulatory standards. The manager will supervise research teams, collaborate with cross-functional departments, and provide strategic direction for clinical research...

Company DescriptionClinSparc MedTech Research LLP is a leading Site Management Organization (SMO) based in Nashik, Maharashtra, dedicated to precision, integrity, and patient-centered care in clinical research. Our GCP-certified professionals and onsite investigators ensure reliable and timely clinical trial results. We bridge the gap between research sites...

Key Responsibilities:We manage project-specific and departmental document tracking and control activities.Clinical data management involves CRF reviews and DMTMF preparation.We work with clients, team members, and PM to resolve issues and coordinate UAT.Data clarification forms are created, reviewed, and tracked.Manual data listings and database validation...

We are seeking a medical professional to fill the role of Clinical Documentation Specialist in Nashik, India.The ideal candidate will have at least 1 year of experience in clinical documentation and coding, specifically in emergency medicine and operating rooms. They should be certified by AAPC or AHIMA with CPC/COC/CCS certifications.Key responsibilities...

Job OverviewWe are seeking a skilled data programming professional to fill this role. The ideal candidate will have hands-on experience with clinical data and excellent programming skills.Key Responsibilities:Data Programming: Develop program listings and mappings, create visualizations, and automate tasks.Data Extraction and Transformation: Configure data...

Job Title: Central Data Integrity Specialist">This role plays a crucial part in ensuring the quality and integrity of clinical trial data through centralized monitoring activities, statistical data review, and proactive risk management.Main Responsibilities:Develop Risk-Based Quality Management (RBQM) plans and conduct study risk assessments to identify...