203 Medidata Jobs - Page 7

Job Title: Director – Clinical Research Location: Greater Noida Experience Required: 5–10 Years in Clinical Research Educational Qualification: Ph.D., MD, or MPH (or equivalent) in a relevant scientific discipline (e.g., Biology, Medicine, Pharmacy) Budgeted CTC: Upto ₹36 LPA Employment Type: Full-Time | Onsite About the University: Our Client is a NAAC A+ accredited, multidisciplinary university in Greater Noida that fosters global learning, cutting-edge research, and innovation. With over 20,000 students from 85+ countries, the university is one of India’s leading education providers with a focus on holistic and interdisciplinary education. Position Overview: We are seeking a highly qualif...

Vasta Bio-Informatics Private LimitedMAHARASHTRA Posted On 20 Jun 2025 End Date 31 Jul 2025 Required Experience 1 - 3 Years Basic Section No. Of Openings 2 Grade C1B Designation Clinical Research Associate Closing Date 31 Jul 2025 Organisational Country IN State MAHARASHTRA City NAVI MUMBAI Location Navi Mumbai-I Skills Skill PHARMACOVIGILANCE CLINICAL RESEARCH MEDICAL WRITING ONCOLOGY CLINICAL DEVELOPMENT CRO GCP EDC CLINICAL DATA MANAGEMENT ICH-GCP Education Qualification No data available CERTIFICATION No data available Job Description Job Title: Clinical Research Associate Department: Delivery Job Location: Navi Mumbai Reporting To: Lead Job Duties / Responsibilities: Project and Operati...

CDC II _ Office Based ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Clinical Data Coordinator II to join our diverse and dynamic team. As a Clinical Data Coordinator II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of inNvative treatments and therapies. What you will be doing Assist Data Management Study Lead in maintenance of eCRF, Data Validation Sp...

CDC II _ Office Based ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Clinical Data Coordinator II to join our diverse and dynamic team. As a Clinical Data Coordinator II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of inNvative treatments and therapies. What You Will Be Doing Assist Data Management Study Lead in maintenance of eCRF, Data Validation S...

About CloudLabs: CloudLabs Inc was founded in 2014 with the mission to provide exceptional IT & Business consulting services at a competitive price, to help clients realize the best value from their investments. Within a short span, CloudLabs evolved from pure-play consulting into a transformative partner for Business Acceleration Advisory, Transformative Application Development & Managed Services - enabling digital transformations, M&A transitions, Automation & Process-driven optimizations & complex Integration initiatives for enterprises across the globe. As a Strategic Planning & Implementation Partner for global companies, CloudLabs has seen a 200% uptake in winning high-value, high-impa...

Data Quality System Testing Expert Location: Remote Objective: The Data Quality System Testing Expert is responsible for leading and executing user acceptance testing (UAT) and validation of clinical study builds in EDC systems (e.g., Veeva CDMS, Medidata Rave). The role ensures study database quality and compliance with technical specifications and regulatory standards, supporting cross-functional teams in delivering accurate, reliable data for clinical trials. Key Responsibilities: Testing Execution & Documentation Create and execute test plans, UAT scripts, and summary reports in Excel or ALM. Develop and execute standardized test cases for EDC components, data listings, and system integr...

Role: Clinical Operations Support Required Technical Skill Set: Highly skilled with Veeva eTMF Application Experience: 5 to 8 Years Work Location: Mumbai, New Delhi, Indore, Bangalore , Hyderabad, Pune, Lucknow, Chennai, Kolkata Desired Competencies (Technical/Behavioral Competency) Must-Have: Experience with R&D specific IT application systems for Document management, trial management, Data management and/or Pharmacovigilance. Experience with data visualization and/or analytics tools and ability to build, program and modify new reports and visualizations. Experience with Clinical Trial related systems, e.g. Clinical Trial Management System (CTMS), electronic Trial Master File (eTMF, prefera...

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a w...

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a w...

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a w...

Description At Quanticate, we're pioneers in providing top-tier statistical and data management support to our clients. We're seeking a dedicated "Clinical Data Manager I" who's committed to upholding the highest standards, following procedures, and ensuring compliance with regulations, all while providing exceptional customer care. As a "Clinical Data Manager I" you will lead, co-ordinate, and action all tasks relating to Clinical Data Management from the start to the finish of a study & to project manage studies across CDM functions. Core Accountabilities Activities required of a Clinical Data Manager I (however not restricted to) are as below: To contribute to the efficient running of the...

Software Engineering Consultant C# We are looking for a skilled Software Engineering Consultant (Study Transfer Developer) to join our Medidata Service team and contribute to the critical Transfer Project. In this role, you will work closely with team members in Pune, India, as well as colleagues in the United States, ensuring seamless collaboration. The Study Transfer Project involves transferring specific client data securely from one client to another, a process that demands careful handling of sensitive information and precision across each transfer step. This position is based in Pune, India. Role Description & Responsibilities Analyze, design, code, test, and debug software solutions t...

We are looking for a skilled Software Engineering Consultant (Study Transfer Developer) to join our Medidata Service team and contribute to the critical Transfer Project. In this role, you will work closely with team members in Pune, India, as well as colleagues in the United States, ensuring seamless collaboration. The Study Transfer Project involves transferring specific client data securely from one client to another, a process that demands careful handling of sensitive information and precision across each transfer step. This position is based in Pune, India. Role Description & Responsibilities Analyze, design, code, test, and debug software solutions to meet business requirements indepe...

At Quanticate, we're pioneers in providing top-tier statistical and data management support to our clients. We're seeking a dedicated "Clinical Data Manager I" who's committed to upholding the highest standards, following procedures, and ensuring compliance with regulations, all while providing exceptional customer care. As a "Clinical Data Manager I" you will lead, co-ordinate, and action all tasks relating to Clinical Data Management from the start to the finish of a study & to project manage studies across CDM functions. Core Accountabilities: Activities required of a Clinical Data Manager I (however not restricted to) are as below: To contribute to the efficient running of the CDM depart...

Premier Research is looking for a Data Management Reporting Programmer (SQL Developer) - Fixed Term Contract - India to join our Functional Services Provider (FSP) team. You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success. We are Built for You. We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires. We are Built by You. Your ideas influence the way we...

Company Description ClinFocus empowers life sciences organizations to accelerate clinical trials through technology-driven solutions. Our services include EDC Development, Systems Integration, AI Deployment & Enablement, Clinical Data Science, Project Management, and Development of Integrated Dashboards. As an ISO-certified organization and partner of Medidata Rave, we are committed to excellence and trust in clinical research. We are seeking a highly motivated and skilled Clinical Statistical Programmer to join our dynamic Biometrics team. In this role, you will be instrumental in the development, validation, and maintenance of programs used for the analysis and reporting of clinical trial ...

Company Description ClinFocus is a life sciences organization that specializes in accelerating clinical trials and enhancing data quality through technology-driven solutions. Our services include EDC Development, Systems Integration, AI Deployment & Enablement, Clinical Data Science, Project Management, and Development of Integrated Dashboards. We are an ISO-certified organization and an accredited partner of Medidata Rave, dedicated to delivering excellence and building trust. ClinFocus is seeking an experienced and highly detail-oriented Quality Assurance Manager to lead and enhance our quality management system across all clinical data management and technology services. This critical rol...

Jd Cdm 3.5 + yrs of minimum Clinical Data Management experience Must have exposure to Study Start up, Conduct and Study Closeout. If not three phases should have good exposure to minimum two phases. Rave (Medidata) or Veeva EDC hands on experience is must. Must Have Setup experience should have knowledge of DMP (Data Management Plan) creation, Edit check creation, Data Transfer specification creation, UAT knowledge (not mandatory). Conduct Experience Data Cleaning experience (Query Handling), Postproduction Changes, SAE reconciliation, LAB Reconciliation, ECOA/EPRO Reconciliation, PK/PD Reconciliation, Dataset review etc . Study Lock Freezing/Locking, should have good experience of Study loc...

Key Responsibilities: Understand and document business and data requirements across clinical domains and translate them into actionable technical tasks Manage and maintain Jira boards for the Data Engineering team: groom stories, track progress, and coordinate with developers, QA, and stakeholders Act as a liaison between product, engineering, and external stakeholders to clarify requirements and ensure alignment across teams Drive the creation and maintenance of data entity mapping documentation between legacy systems and Medidata CTMS Collaborate with engineering leads to support ETL and data pipeline validation, including defining edge cases and expected behaviors Support UAT efforts for ...

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 management activities, timelines and deliverables. Key Tasks & Responsibilities Design/develop and test clinical databases including forms, folders, matrices, data dictionaries, unit dictionaries, edit checks, derivations, custom functions, standard and custom reports Performs peer review for the studies built by other Clinical Database ...

Skill required: Clinical Data Services - Clinical EDC Build Designation: Clinical Data Svs Analyst Qualifications: BSc/Master of Pharmacy Years of Experience: 3 to 5 years Language - Ability: English(International) - Expert About Accenture Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song— all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenui...

Job Title: Associate Director, GCS Business Technology Solutions Introduction to role: Are you ready to make a significant impact in the world of Biopharma Clinical Operations? As an Associate Director in GCS Business Technology Solutions, you'll be at the forefront of driving industry-leading processes, technology, and services. Your role will be pivotal in owning the lifecycle management and continuous improvement of specific clinical operations processes, systems, or services. Collaborate with internal and external stakeholders to ensure customer needs are met and optimize the delivery of clinical studies. You'll identify and deliver improvements using tools like Lean Six Sigma to improve...

Job ID R-228515 Date posted 06/09/2025 Job Title: Associate Director, GCS Business Technology Solutions Introduction to role: Are you ready to make a significant impact in the world of Biopharma Clinical Operations? As an Associate Director in GCS Business Technology Solutions, you'll be at the forefront of driving industry-leading processes, technology, and services. Your role will be pivotal in owning the lifecycle management and continuous improvement of specific clinical operations processes, systems, or services. Collaborate with internal and external stakeholders to ensure customer needs are met and optimize the delivery of clinical studies. You'll identify and deliver improvements usi...

Job Summary: We are seeking a Medidata eTMF/CTMS Product Consultant to support the implementation and use of Medidata eTMF/CTMS Key Responsibilities Implement and support Medidata eTMF/CTMS Perform configuration changes. Oversee master data creation and study setup. Manage user access, roles, and permissions. Perform data reconciliation and cleanup. Generate report dashboards in Visual Analytics. Troubleshoot user issues and submit enhancements. Ensure compliance with regulatory standards. Conduct user training sessions. Collaborate with cross-functional teams. Generate user training manuals. Qualifications Bachelor's degree in Life Sciences, IT, or related field. 6+ years of relevant IT exp...

Company Description ClinFocus is a leading provider of technology-driven solutions and expert services for life sciences organizations to accelerate their clinical trials and gain deeper insights. Our services include EDC development, systems integration, AI deployment & enablement, clinical data science, project management, and development of integrated dashboards. As an ISO-certified organization and an accredited partner of Medidata Rave, ClinFocus is dedicated to delivering excellence and building trust through exceptional work ethics and ownership. Role Description This is a full-time remote role for a Clinical Systems and Data Manager. The Clinical Systems and Data Manager will be resp...