203 Medidata Jobs - Page 8

Looking for experienced Full Stack engineer who is passionate about application development. Primary responsibilities will include hands-on development of Medidata's software applications with Java, Clojure, Python, R, React/Typescript, and Amazon Web Services. Responsibilities 8+ years hands on experience in Java , ready to shift gears to Clojure (a must), python as needed Working experience with AWS (cloud watch , Lambdas, Sagemaker, familiar with container orchestration ECS / EKS) . Proficient in React, including both class components and hooks Strong understanding of Redux for state management (actions, reducers, middleware) Experienced with TypeScript in large-scale front-end applicatio...

Job title : Data Validation Team Member Hiring Manager: Project Lead-ESR & Grants Location: Hyderabad % of travel expected: Travel required as per business need Job type: Permanent and Full time About The Job Our Team: Sanofi Business Operations (SBO) is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions . Sanofi Business Operations strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, globally. The Sanofi Business Operations is built to reduce reliance on exter...

Job Title: Legal & Contract Manager – Biologics & CRO (Legal Focus) Location: Vapi, Gujarat About the Role We are seeking an experienced Contract Manager with a strong background in legal writing to support global contract management for clinical research organizations (CROs) and pharmaceutical/biologics programs. The role involves drafting, reviewing, and negotiating complex agreements within regulated environments, collaborating cross-functionally with legal, clinical, procurement, and business development teams. Key Responsibilities Draft, review, and negotiate a wide range of agreements including: Clinical Trial Agreements (CTAs) Confidentiality Disclosure Agreements (CDAs) Master Servic...

As a Medical Coding Specialist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Location: Remote Shift: 2pm-11pm IST What You Will Be Doing Coding performed in accordance with departmental coding conventions and company SOPs. The coder will generate queries for clarification of potentially discrepant data. Ability to work in cross-functional team-oriented environments. Assist with data coding consistency reviews and SAE reconciliation, as needed. The Coder will collaborate with medical monitors, Clinical and Data Management team members, as required, to ensure the timely processing of coding, according to project...

Bangalore Karnataka India Job Type: Regular Full-time Division: Precision for Medicine Business Unit: Clinical Solutions Requisition Number: 5467 Position Summary: The Senior/Principal Clinical Database Manager is responsible for the design, development, testing, implementation, maintenance and support of clinical databases and applications. Position will interface directly with the internal team (i.e. Data Management, Project Management, etc.), EDC vendor, clients and third-party vendors to gather requirements and provide status updates. Provides operational and technical training to end users and junior staff. Additionally, the Senior/Principal Clinical Database Manager may play a lead rol...

Bangalore Karnataka India Job Type: Regular Full-time Division: Precision for Medicine Business Unit: Clinical Solutions Requisition Number: 5543 Job Description Position Summary The primary responsibility of the Clinical Systems Administrator is to provide business administration support for the Sponsor’s clinical systems, including but not limited to eTMF/CTMS, IRT and EDC systems (i.e., Veeva Clinical Vault and Medidata CTMS). The Clinical Systems Administrator will work with the Clinical Systems Manager/Sr. Manager and Project teams to ensure on-time deliverables and provide clinical systems user support as outlined below. Essential functions of the job include but are not limited to: Re...

Location: Pune-Kothrud/Wakad(Offline/Online) Experience: 2-3 yrs Qualification: Graduate/Post Gradu Job Description: Job Summary: We are seeking a highly qualified and experienced Clinical Data Management (CDM) Trainer to deliver a structured and in-depth curriculum covering Clinical Research, Drug Development, GCP-ICH Guidelines, Clinical Data Management, Pharmacovigilance, and Regulatory Affairs. The ideal candidate should have a strong background in clinical research and data management with proven experience in training or academic instruction. Key Responsibilities: Design, update, and deliver training content aligned with the clinical data management curriculum. Conduct engaging classro...

Our clinical activities are growing rapidly, and we are currently seeking a full-time, office-based Data Coordinator to join our Data Management team in India, Mumbai. If you want an exciting career where you can develop and grow your career even further, then this is the opportunity for you. Responsibilities Track and maintain metrics regarding the status of the data within EDC systems Clean the clinical database, which includes generating and resolving data clarifications Reconcile clinical data Assist with support activities for the Data Management department Qualifications Bachelor’s degree in life science/ pharmacy/ health related field with strong attention to detail and working knowle...

eClinical Solutions helps life sciences organizations around the world accelerate clinical development initiatives with expert data services and the elluminate Clinical Data Cloud – the foundation of digital trials. Together, the elluminate platform and digital data services give clients self-service access to all their data from one centralized location plus advanced analytics that help them make smarter, faster business decisions. Overview The Manager of Data Management assumes operational leadership in overseeing the end-to-end data management services across designated projects and studies in the realm of modern clinical data management. This role entails close collaboration with clients...

Hi, We are hiring for Leading ITES Company for Lead Data Manager Profile. Job Description Perform day to day Clinical Data Management activities. Work and coordinate with the team to perform data management activities and deliver an error free quality database in accordance with the data management plan and regulator standards. Read and understand the study protocol and the timelines. Perform test data entry in TEST environment, data listing review, data reconciliation and query management tasks. Escalate/Action discrepancy in the clinical data as appropriate. Perform external checks to handle manual discrepancies and action the same. Ensure an error free, quality data with no open queries. ...

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-impact and high-risk ...

Hi, We are hiring for Leading ITES Company for Lead Study Data Manager Profile Skills: a) Minimum 5 Years of Core Clinical Data Management Experience with minimum 1 year of experience of leading a clinical trial. . b) Experience on Study Conduct and Close Out c) Any Graduate JOB DECSRIPTION: Need exposure of Inform or Medidata Rave database Responsible & Accountable for the assigned study conduct activities, in clinical trials Validate clinical trial data to ensure consistency, integrity and accuracy based on project specific guidelines. Generate data queries based on validation checks or raise Manual queries to resolve data inconsistencies. To perform reconciliation of data from external so...

Our global activities are growing rapidly, and we are currently seeking a full-time, Pune-based Clinical Database Programmer to join our Biometrics team. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. Responsibilities Develop, program, validate and maintain clinical trial databases according to company standards; Maintain and contribute to company library of standard CDASH compliant CRFs ; and Act as primary contact to the data management team for assigned studies, supp...

eClinical Solutions helps life sciences organizations around the world accelerate clinical development initiatives with expert data services and the elluminate Clinical Data Cloud – the foundation of digital trials. Together, the elluminate platform and digital data services give clients self-service access to all their data from one centralized location plus advanced analytics that help them make smarter, faster business decisions. Overview Quality Control Specialists are operationally responsible for performing quality control activities associated with Biometrics client’s deliverables. Quality Control Specialists will maintain project level perspective, focus, and communicate effectively ...

Job Title: Associate Director, Statistical Programming Introduction to role The Associate Director of Statistical Programming will oversee statistical programming activities for multiple clinical studies, maintain programming infrastructure, and ensure compliance with SOPs to produce quality and timely deliverables. This role requires extensive experience and proven skills in the use of SAS within a Statistical Programming environment, along with a complete understanding of statistical programming processes, procedures, and roles. The successful candidate will support Biostatistics in statistical analysis, including generating analysis data listings, tables, and figures, and creating all fil...

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...

Description Clinical Programmer II Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innova...

Job Summary We are seeking a dedicated Product Specialist with 3 to 6 years of experience to join our team. The ideal candidate will have strong technical expertise in RAVE and Medidata Rave and it is beneficial if they have experience in Research and Development. This hybrid role offers the opportunity to work both remotely and on-site with a day shift schedule. No travel is required. Responsibilities Oversee the implementation and maintenance of Medidata Rave systems to ensure seamless operation and data integrity. Provide technical support and troubleshooting for RAVE-related issues to ensure minimal downtime and maximum efficiency. Collaborate with cross-functional teams to gather requir...

Our global activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Database Programmer to join our Biometrics team. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. Responsibilities Develop, program, validate and maintain clinical trial databases according to company standards; Maintain and contribute to company library of standard CDASH compliant CRFs ; and Act as primary contact to the data management team for assigned studies, su...

About Birlasoft Ltd. Empowered By Innovation Birlasoft, a global leader at the forefront of Cloud, AI, and Digital technologies, seamlessly blends domain expertise with enterprise solutions. The company’s consultative and design-thinking approach empowers societies worldwide, enhancing the efficiency and productivity of businesses. As part of the multibillion-dollar diversified CKA Birla Group, Birlasoft with its 12,000+ professionals, is committed to continuing the Group’s 170-year heritage of building sustainable communities. Role: Assistant Manager Experience: 4 to 6 Years in Bid Management Industry: Life Sciences Location: Noida, Mumbai, Pune & Bengaluru Must Have Manage the end-to-end b...

Location Bengaluru, Karnataka, India Job ID R-227172 Date posted 19/05/2025 Job Title: Associate Director - Statistical Programming Work Location: Manyata Tech Park, Bangalore, India Work Schedule: Three days on-site, two days remote (3/2) Career Level: E – Individual Contributor position. Introduction to role The Associate Director of Statistical Programming will oversee statistical programming activities for multiple clinical studies, maintain programming infrastructure, and ensure compliance with SOPs to produce quality and timely deliverables. This role requires extensive experience and proven skills in the use of SAS within a Statistical Programming environment, along with a complete un...

Location Chennai, Tamil Nadu, India Job ID R-220063 Date posted 14/05/2025 Job Title - EDC IT Platform Engineer Career Level - D1 Introduction to role Are you ready to make a difference in the world of medicine? AstraZeneca is seeking an EDC IT Platform Engineer to join our R&D IT: EDC Product Engineering Team. You'll play a crucial role in managing, improving, and maintaining our EDC product, Medidata’s Rave, which is GxP compliant and integral to our Clinical Development Platforms. Collaborate with multi-functional teams, including IT Product Leads, DevOps Leads, and business teams, to support the EDC Product across all therapeutic areas. Accountabilities Facilitate key discussions with pa...

Description Senior Clinical Programmer (Spotfire/Cluepoints) Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passiona...

Hi, We are hiring for Leading ITES Company for Lead Study Data Manager Profile Skills: a) Minimum 5 Years of Core Clinical Data Management Experience with minimum 1 year of experience of leading a clinical trial. . b) Experience on Study Conduct and Close Out c) Any Graduate JOB DECSRIPTION: Need exposure of Inform or Medidata Rave database Responsible & Accountable for the assigned study conduct activities, in clinical trials Validate clinical trial data to ensure consistency, integrity and accuracy based on project specific guidelines. Generate data queries based on validation checks or raise Manual queries to resolve data inconsistencies. To perform reconciliation of data from external so...

Description Investigator Management Solutions (IMS) Specialist II Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with pas...