Senior Clinical Data Co-ordinator

As a Senior Clinical Data Co-ordinator, you will be the primary point of contact for data management activities related to the study. Your responsibilities will include overseeing and coordinating tasks assigned to the study team members, providing training to new data management personnel, and planning, managing, and performing data processing and management activities for assigned projects. Key tasks will involve creating and developing study specifications, implementing and testing eCRF or paper CRF edit checks, authoring and reviewing the Data Management Plan (DMP), designing and reviewing case report forms (CRFs/eCRFs), and participating in the database design process including User Acceptance Testing (UAT). You will review data, resolve queries, assist in resolving medical coding discrepancies, validate electronically captured data, and write clear queries on missing data and data points failing pre-defined range checks and/or logical checks. Additionally, you will cooperate with the Quality Assurance Department on quality control audits, review database edit check specifications, and lead efforts in developing and maintaining standard database integrity checks. Furthermore, you will define and monitor clinical trial data flow and quality control processes in accordance with corporate Standard Operating Procedures (SOPs), provide training to new staff and study site personnel on data management processes and procedures, and assist in the recruitment process by conducting interviews and shortlisting candidates. Desirable Skills and Experience: - Experience in Clinical Data Management - Bachelors Degree in Pharma - Junior level experience in Clinical Research Location: Chennai, India Employment Type: Full Time In this role, you will play a crucial part in ensuring the accuracy and compliance of data management processes for clinical trials. Your expertise and attention to detail will contribute to the success of the study and the overall advancement of clinical research.,