Clinical Data Coordinator

Role & responsibilitiesPlan and execute clinical validation studies, including protocol development, data collection, and analysis.Coordinate with hospitals/clinicians for clinical simulation, usability, and in-hospital evaluations.Supporting on preparation of Clinical Evaluation Report, clinical validation report for regulatory submissionPrepare informed...

Clinical Research Coordinator (CRC) manages and coordinates the day-to-day operations of a clinical trial, which includes recruiting and screening participants, obtaining informed consent, collecting and managing data, and ensuring compliance with study protocols and regulations. They also act as a liaison with sponsors, investigators, and regulatory bodies,...

About the Role We are seeking a Clinical Data Co-ordinator to take ownership of data management activities for our ongoing clinical studies. The role requires end-to-end responsibility for data collection, cleaning, storage, quality control, and preparation of datasets for analysis, ensuring accuracy, integrity, and compliance with research standards. Key...

Position OverviewWe are seeking an experienced Clinical Data Specialist II to join our clinical research team in Chennai. The successful candidate will be responsible for accurate and timely data entry into Electronic Data Capture (EDC) systems from various e-source documents, including real-time data and Clinical Research Information Officer (CRIO) sources....

Position OverviewWe are seeking an experienced Senior Clinical Data Manager to support our clinical data management team in Chennai. The successful candidate will work as Subject Matter Expert (SME) for CRIO CTMS including e-Source creation, edit, oversee and mentor the end-to-end clinical trial management system activities, ensuring seamless integration...

Position OverviewWe are seeking an experienced Associate Manager - CDM to support our clinical data management team in Chennai. The successful candidate will work as Subject Matter Expert (SME) for CRIO CTMS including e-Source creation, edit, oversee and mentor the end-to-end clinical trial management system activities, ensuring seamless integration between...

Ensure the integrity of data and that the study is conducted in compliance with approved protocol, GCP, applicable regulations, and internal SOPsPrepare and maintain documents related to clinical trials.Generate data entry queries and test clinical applications for numerous clinical trials.Analyze clinical trials data and prepared reports for Data...

Key Responsibilities:Bachelor's degree in Life Sciences, Computer Science, or related field.8+ years of experience in clinical data testing and validation.Perform UAT for CRF screens, database edit checks, and exceptional reports/listings.Test clinical study setup configurations including protocol parameters, visit schedules, and form designs.Validate...

Job Description We are seeking a highly organized and proactive Clinical Research Assistant to support the daily operations of our longitudinal clinical trials. The study involves Continuous Glucose Monitoring (CGM), lab testing, gut microbiome analysis, and remote consultations with physicians. The ideal candidate will play a critical role in...

Responsibilities:* Collaborate with cross-functional teams on study setup, data cleaning, and reporting.* Manage clinical data from CRFs using RAVE software following ICH-GCP guidelines.Health insuranceAnnual bonusProvident fundAccidental insuranceLife insuranceMobile bill reimbursements