10,018 clinical data manager jobs in India.

... experience\ **Salary Range:** ₹9–20 LPA\ **Band:** BPO 3/4/5/6\ **Locations:** Mumbai / Pune / Bangalore / Noida\ **Shift:** General Shift\ **Reporting To:** Delivery Manager ## Job Summary We are looking for skilled Statistical Programmers with experience in SAS programming, clinical trial data analysis, and statistical reporting ...

... product and engineering leaders to define problems, shape roadmaps, and agree on success measures across your product areas ● Use customer research, product data, and domain knowledge to challenge assumptions and guide decisions ● Bring coherence to data-dense clinical and operational workflows, including permissions exceptions, ...

Assistant Manager, Sales position in Nasik, India focused on driving pharmaceutical product sales across the Marathwada region. Responsible for building healthcare professional relationships, managing territory development, and achieving sales forecasts for Baxter's medical product portfolio. Responsibilities - Drive sales ...

... create a thriving ecosystem that delivers accessible high-quality and sustainable healthcare for all. Position Summary : We are looking for a Senior Product Manager to join our Value-Based Care Analytics & Performance team within our Clinicals division in Bangalore . In this role you will be responsible for defined problem ...

... automation and program roles. - Strong knowledge on SDLC, PRD process, Risks, FMEAs. - Awareness of patient-data privacy, cybersecurity and secure handling of clinical information. - Knowledge of healthcare interoperability standards such as DICOM, HL7 and FHIR. - Experience with real-time clinical data, device connectivity, ...

... Sciences Domain : - Good understanding of pharmaceutical industry data and business processes, preferably across Commercial, Sales, Marketing, Patient Services, Clinical, or R&D domains.- Exposure to pharma datasets, data integration challenges, industry-specific business rules, and data governance https://jobeax.com/link/jd7RJPTFkCOnxWn2 ...

... Vault Quality Suite, Safety Suite, RIM Suite, Clinical Suite - Drive requirements management, including workshops for as-is/to-be analysis, workflow design, and data mapping between legacy and Veeva systems. - Oversee data migration and system integration planning, ensuring alignment with business processes and compliance ...

Pfizer seeks a Senior Associate for Central Monitoring and Data Surveillance in clinical data sciences. This role involves establishing and maintaining risk-based monitoring systems, ensuring data quality and regulatory compliance across clinical trial databases, and coordinating with global study teams to manage signals ...

... you. Prudentia, a PrimeVigilance company, is where safety science meets technology. We advise pharmaceutical companies on the processes and systems behind clinical and post-marketing safety, from selecting and implementing safety databases to managed services, data migration and turnkey tools that close the gaps in leading ...

... records, alongside molecular and imaging https://jobeax.com/link/BWpQKGsB5IG4pVxY flagship platform, nSights, gives researchers access to de-identified real-world data across clinical, molecular and imaging modalities, covering more than 20 years of data and over 11 million patient records. We work with leading academic health ...

... records, alongside molecular and imaging https://jobeax.com/link/BWpQKGsB5IG4pVxY flagship platform, nSights, gives researchers access to de-identified real-world data across clinical, molecular and imaging modalities, covering more than 20 years of data and over 11 million patient records. We work with leading academic health ...

... teams across focus geographies. The role requires close collaboration with internal Intuitive stakeholders including other marketing departments capital and clinical sales training clinical affairs legal regulatory and compliance to execute key initiatives such as: - Engage in market research activities for lead generation. ...

Senior Manager, Finance ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, ...

... Degree in technology, statistics, pharmaceutics or another related science or mathematics field with a minimum of 8 years of SAS programming experience with clinical trial data OR Master's Degree in technology, statistics, pharmaceutics or another related science or mathematics field with a minimum of 6 years of SAS programming ...

... on its customers, employees, and communities. The Role Veeva is looking for a highly motivated individual with life science industry experience within the Clinical Data domain. You will drive impactful product communication and champion customer success with our Clinical Data Management applications, Veeva EDC and Veeva ...

... and delivering impactful, compliant engagement. You will focus on achieving sales and growth objectives through effective multi-channel customer interactions, data-driven insights, and close collaboration with cross-functional teams. If you are looking to launch a new product in a specialty portfolio in a priority TA and ...

... and stakeholder feedback to optimise targeting, messaging, content, timing and channel investment. - Coordinate priorities and approvals with the Operations Manager, Lead Recruiter and part-time Marketing Director. - Promote consistent brand and messaging standards and ensure agreed approval and data-handling processes ...

... stakeholders, including their needs and priorities. • Creates annual segment/account plans with financial targets and clear roadmap for achieving targets. • Maintains a database of intelligence on competitor activity and strategy within the account. • Provides regular cadence with all aligned members of the customer/segment account. ...

... excellence. Researches, writes, and edits clinical study reports and study protocols, and summarizes data from clinical studies. Researches, writes, and edits clinical study reports and study protocols, and summarizes data from clinical studies. - Serves as primary author who writes and provides input on complex clinical and ...

... Precision and attention to detail in preparing regulatory documentation and ensuring compliance. - Familiarity with electronic submission standards (eCTD, NeeS) and data standards (IDMP, xEVMPD). - Ability to work collaboratively with cross-functional teams across clinical, regulatory, and quality domains. - Commitment to high ...