Clinical Data SME Leader

At Emerald Clinical, we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region. We are dedicated to advancing clinical research through scientific expertise and operational excellence, supporting biopharmaceutical, medical device, and diagnostic customers across all trial phases, from registration to...

About Triomics:Triomics is building the modern technology stack for oncology trial sites and investigators that unifies the workflows of clinical care and clinical research, moving the healthcare industry closer to the vision of Clinical Research as a Care Option. Our platform, which is based on our proprietary oncology-focused large language model (OncoLLM)...

Part of the Oncology Clinical Team, working on building and developing Oncology Data dictionaries, liquid tumor pipeline from scratch and SOP creation by acting as an SME for the liquid tumor portfolio, along with secondary duties of Curation/Abstraction etc. Position Summary: We are seeking a highly skilled and experienced Data Curation Subject Matter...

Job Title: Clinical Research Associate (CRA)Company: MS Clinical Research Pvt LtdAbout Us:MS Clinical Research (MSCR) is a leading clinical research organization dedicated to advancing scientific discovery and improving healthcare outcomes. We are committed to conducting high-quality clinical trials and contributing to the development of innovative medical...

About Company Our Client delivers a comprehensive integrated suite of cloud-based technologies and services that enable specialty groups to optimize clinical and financial performance as reimbursement shifts to value-based models Connected by the IntegraCloud platform the company s core applications span population health including care management ...

Clinical Database Programmers are operationally responsible to provide technical support and oversight for the Medidata Clinical Cloud (MCC) implementation activities. Clinical Database Programmers will maintain project level perspective, focus and communicate effectively as the MCC SME on technical and functional electronic data capture programming and data...

Job Summary: We are looking for a highly skilled Pharmaceutical Subject Matter Expert (SME) to provide deep industry knowledge and strategic guidance in pharmaceutical operations, technology, compliance, and digital transformation. The SME will work closely with cross-functional teams, helping drive innovation, regulatory adherence, and efficiency across...

Key Responsibilities:Requirements Gathering & Documentation: Collected, analyzed, and documented healthcare software requirements; created BRD, FRS, DFD, user manuals, and test cases; ensured client alignment and regulatory compliance (NABH, NABL, GCP).Testing & Quality Assurance: Conducted manual testing, coordinated UAT with clients, tracked metrics,...

Are you passionate about working with data?Data Associate RoleThis is an exciting opportunity to develop key skills in clinical data management within a regulated and fast-paced environment. As a Data Associate, you will play a critical role in ensuring accurate and compliant data management for clinical trials.Enter and verify clinical data from Case Report...

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 a Senior Clinical Data Manager I to join our A-team. The Senior Clinical Data Manager I (SrCDM1) is responsible for leading data...