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At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. We are looking for Clinical Data Manager III (CDM III) to join our A-team. As CDM III at Allucent, you will manage and coordinate DM deliverables from database design & set-up, through cleaning and reporting to database locking, ensuring that the completeness, accuracy and consistency of clinical data meets the quality standards and regulatory requirements for analysis and reporting.    PLEASE NOTE: This is not a remote position and we are looking for a candidate who can work from the office (Chennai Location). In this role your key tasks will include: Lead and serve as primary contact for DM with all relevant parties both internally (e.g. Clinical Programmers, Data Scientists, Project Management, Clinical Operations/Monitoring, Clinical Monitoring, Biostatistics and other functional groups) and externally (e.g. sponsors, vendors (EDC, external data), and investigational sites)     Plan and project the resources required including management of tasks, timelines, risk and quality    Monitor tasks against and keep track on budget, forecasts, identify and trigger changes of scope requests   Develop, review and maintain project-specific DM documents including data management plan (DMP), eCRF specifications, data validation plan (DVP) and external data transfer agreements    Lead and coordinate the development of clinical study database set-up, including eCRF design and database validation requirements    Participate in the review of study documents (e.g. protocol, Project Plan, safety plans/manuals and statistical analysis plan), lead and coordinate the review of (electronic) case report forms (eCRFs)    Coordinate, participate and complete the database User Acceptance Testing (UAT) related tasks    Create training materials for EDC users and provide project-specific training as required   Review and validate clinical data to ensure consistency, accuracy, integrity and completeness   Create data cleaning strategy in consultation with applicable functional groups and oversee data releases (such as for DETC/DSMB/IDMC, interim and final locks, updates after lock)  Perform and/or coordinate various data transfers and reconciliation activities including (but not limited to) SAE, PK, and (other) external laboratory data   Create and review project metric reports, status updates, study progress to Lead DM in order to share information on site performance issues, data trends and protocol non-compliance  Support and conduct Quality Review checks during study. As lead DM, may organize and lead Quality Review activities   Assist in contracts negotiation and contracting process with vendors (EDC, IRT, eCOA)  Manage the database maintenance, lock and close-out processes and procedure  Participate in conference calls and/or meetings with vendors and sponsors  Recognize and solve potential problems and evaluate effectiveness  Maintain DM study documentation on an ongoing basis and ensure that all filing is up to date    Plan and create necessary documentation to support internal and external audits; may participate in such audits assigned  Help to align data management and clinical programming best practices, standards and conventions within the company  Propose and support initiatives for improving efficiency. Requirements To be successful you will possess: Minimum Educational Requirement: Preferably Life science graduate or equivalent qualification 6+ years’ experience in clinical data management experience within Contract Research Organization (CRO), Pharmaceutical or biotech indu