7 Clinical Databases Jobs

Job Description: As a Clinical Data Associate II, you will provide data management support and assistance throughout the clinical trial data management process for assigned projects under direct supervision. You will be responsible for following Standard Operating Procedures (SOPs), regulatory directives, study specific plans, and guidelines. Your duties will include supporting the Lead DM, performing data entry for paper-CRF studies, conducting quality control of data entry, developing CRF specifications, assisting in building clinical databases, maintaining quality controlled database build documentation, specifying requirements for edit check types, creating and revising data management d...

Position: Clinical Database Programmer *** JOB DESCRIPTION *** OVERVIEW The Clinical Programmer is responsible for developing and maintaining clinical trial programming, ensuring data integrity, and supporting data analysis for clinical studies. The role involves working closely with biostatisticians, clinical data managers, clients and other stakeholders to ensure that all programming tasks are executed accurately and efficiently across all Biometrics Services projects. The Clinical Programmer is accountable for quality, timely and efficient delivery of project programming tasks and quality information management. KEY TASKS & RESPONSIBILITIES • Read and understand clinical study protocols t...

As a Data Coordinator at Medpace, you will be part of the Data Management team based in India, Mumbai. Your primary responsibility will be to track and maintain metrics of data within EDC systems, clean the clinical database, reconcile clinical data, and assist with support activities for the Data Management department. Key Responsibilities: - Track and maintain metrics regarding the status of data within EDC systems - Clean the clinical database, including generating and resolving data clarifications - Reconcile clinical data - Assist with support activities for the Data Management department Qualifications: - Bachelor's degree in life science/pharmacy/health-related field with strong atten...

Job Description (but not limited to) Responsible for project-specific and departmental document tracking and control activities Reviews CRF (as per protocol) and project-specific documents Responsible for initiating project-specific DMTMF (Data Management Trial Master File) and e-filing and reviewing it on an ongoing basis. Responsible for preparing project-specific documents. Handling requests/issues by the client and team, in coordination with PM. Coordinates with CDA in User Acceptance Testing (UAT) leading to robust database design. Performs procedure verification as a part of database validation. Responsible for creating, reviewing, processing and tracking of Data Clarification Forms an...

As a Regulatory Toxicology & Pharmacology professional in Kolkata, you will be expected to have a clear understanding of Regulatory Toxicology & Pharmacology principles with robust domain knowledge. Additionally, you should possess a good understanding of OECD guidelines Safety Guidelines and be familiar with risk assessment, Hazard assessment, Exposure assessment & Safety assessment. Your role will also require knowledge of various Toxicology/ Pharmacology/ clinical/ Regulatory databases and dose calculation & conversions. With 2-3 years of experience, you should have the capability of interpretation of results and analysis of key toxicity data. Qualifications required for this position inc...

You will be responsible for project-specific and departmental document tracking and control activities. This includes reviewing CRF and project-specific documents as per the protocol. Additionally, you will initiate project-specific DMTMF and e-filing, reviewing it regularly. Your role will involve preparing project-specific documents and handling requests/issues from the client and team in coordination with the Project Manager. You will collaborate with CDA in User Acceptance Testing (UAT) to ensure a robust database design. As part of database validation, you will perform procedure verification and create, review, process, and track Data Clarification Forms. This is crucial for updating cl...

Premier Research is seeking an Associate Database Developer for an 8-month contract in India to join the Functional Services Provider (FSP) team. In this role, you will contribute to the transformation of life-changing ideas from biotech, medtech, and specialty pharma companies into new medicines, devices, and diagnostics. Your work will play a crucial role in saving and enhancing lives, and we value our team members as our most important asset for achieving success. We are committed to supporting your growth, providing you with the necessary skills and opportunities to thrive at work while maintaining the flexibility and balance that your life demands. Your input shapes our work culture, an...