619 Clinical Data Jobs - Page 6

About the Role: We are seeking a compassionate and dependable Patient Care & Support professional to assist patients with daily activities and ensure a comfortable, safe, and healing environment. You will work under the supervision of registered nurses and medical staff to provide direct care and emotional support to patients in a healthcare setting. Key Responsibilities: Measure and record vital signs (temperature, pulse, blood pressure, respiration) Collect samples for lab tests (under supervision) Monitor patient behavior and report changes to nurses or doctors Assist in preparing patients for examinations or procedures Maintain logs of patient care activities and vital signs Report unusu...

Must have experience in any of the EHR platforms (Nextgen, Epic, Athena, eClinicalWorks, Dr.Chrono, Cerner, Medent, Veradigm) Analyze patient medical information on EHR platforms. Enter & update patient data accurately based on predefined rules. Required Candidate profile Good verbal communication skills, may have to communicate with US team members Ability to perform repetitive tasks with consistency Willing to work in night shift (8 PM to 4 AM) Cab will be provided

As a Data Coordinator at Medpace, you will be part of the Data Management team based in India, Mumbai. Your primary responsibility will be to track and maintain metrics of data within EDC systems, clean the clinical database, reconcile clinical data, and assist with support activities for the Data Management department. Key Responsibilities: - Track and maintain metrics regarding the status of data within EDC systems - Clean the clinical database, including 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 atten...

Manage and maintain clinical trial data in compliance with regulatory standards (GCP, ICH). Perform data validation, discrepancy management, and query resolution.

Ensure the integrity of data and that the study is conducted in compliance with approved protocol, GCP, applicable regulations, and internal SOPs Prepare and maintain documents related to clinical trials. Generate data entry queries and test clinical applications for numerous clinical trials. Analyze clinical trials data and prepared reports for Data Coordinator and Sponsor. Serve as liaison between Data Management and other departments in Clinical application developments. Manage clinical research data for the new and ongoing electronic clinical trials. Conduct UAT Testing and validate software application processes for the management of clinical trials. Assist with the creation of data man...

Position Overview The CRIO & eSource Tool Specialist is responsible for the end-to-end management of the CRIO platform, with a strong emphasis on eSource creation, template design, and system administration. This role ensures that study teams are equipped with accurate, compliant, and protocol-specific eSource documents to support efficient, high-quality clinical trial execution. The Specialist will serve as the primary point-of-contact for CRIO tool usage across research sites, providing system configuration, troubleshooting, and training. Candidates with prior experience in clinical trials, interventional studies, and eSource systems are highly preferred. Key Responsibilities System Admini...

Job Description Summary GE Healthcare s Monitoring Solutions (MS) team is seeking a Senior Software Engineer Automation with a strong background in test automation and system verification. In this role, you will contribute to the development of a cutting-edge Digital Health Software platform that delivers clinical intelligence at the point of care. This hospital-wide solution is mobile, cable-less, and cloud-enabled redefining the future of patient monitoring. Join us in driving the Digital Industrial transformation at GE Healthcare, where innovation meets impact. About Monitoring Solutions: GE Healthcare s MS business is a global leader in technologies for acquiring, analyzing, and integrat...

Role & responsibilities : Supports development of specifications for technical data management processes and systems Contribute to the Request for Proposal (RFP) and Request for Information (RFI) process. Prepares input for and participates in proposal bid defense meetings where appropriate Acts as Subject Matter Experts (SME) for designated systems/databases used by Data Management (DM) Supports DM to ensure processes in relation to systems/databases are consistent and that best practices are maintained globally. Can consult with internal functional teams and sponsors as a SME Assists with developing, monitoring and enforcing productivity, quality standards and efficiencies, input into the ...

Lead Clinical Data Science Programmer, Bangalore, India ICON plc is a world-leading healthcare intelligence and clinical research organization Were 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, ICON PLC is seeking a highly skilled and experienced Senior Lead Clinical Data Science Programmer to join our team The ideal candidate will have over 4 years of experience working within Data Warehouse platforms in a regulated industry, specifically within a clinical trial environment (IDAR) This role demands a deep understanding of data visualization tools, scripting languages, and ...

Job Summary - Hands on working experience in EHR / EMR Application clinical data analysis and support activities - Experience in Netsmart myAvatar application support is a plus - Experience in Mental healthcare and behavioral healthcare workflows & data management - Experience in EHR / EMR application troubleshooting - Knowledge of USA healthcare workflows & HIPAA compliance would be a plus - Proficient communication and interpersonal skills to manage calls and interact with physicians, nurse practitioners, and other healthcare personnel - Good technical skills

About Founda Health At Founda, were driven by a deep curiosity about the future of healthcare. Our mission is to build the global infrastructure that empowers innovators to shape tomorrows healthcare system. Were not just participating in the healthcare technology revolution; we are leading it. As a global player in data exchange between healthcare institutions, we facilitate the coordination of patient care and streamline the flow of data between healthcare facilities and applications. Our mission is to set the standard for data availability in healthcare. By combining our platform for data access with the newly acquired platform for data exchange, including image and document exchange, wer...

Skill required: Clinical Data Services - Clinical eTMF Management Designation: Clinical Data Svs Associate Qualifications: BTech/Bachelor of Pharmacy/Master of Pharmacy Years of Experience: 1 to 3 years What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the worlds leading biopharma companies bring their vision to life enabling them to improve outcomes by conv...

Skill required: Clinical Data Services - Clinical Data Management Designation: Clinical Data Svs Associate Qualifications: BTech/Bachelor of Pharmacy/Master of Pharmacy Years of Experience: 1 to 3 years What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the worlds leading biopharma companies bring their vision to life enabling them to improve outcomes by conv...

Skill required: Clinical Data Services - Clinical Data Management Designation: Clinical Data Svs Sr Analyst Qualifications: Bachelor of Pharmacy/Master of Pharmacy Years of Experience: 5 to 8 years What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the worlds leading biopharma companies bring their vision to life enabling them to improve outcomes by convergin...

Job Description: As a Medical Representative, your role involves promoting and selling pharmaceutical products or medical devices to healthcare professionals. You will be responsible for building strong relationships with key stakeholders and achieving sales targets. Acting as a liaison between the company and the medical community, you will provide product information, clinical data, and support to drive product adoption and meet customer needs. Key Responsibilities: - Present and demonstrate pharmaceutical products or medical devices to doctors, pharmacists, and other healthcare professionals, highlighting benefits, features, and clinical evidence. - Achieve sales goals by identifying cust...

Role & responsibilities : 1. Collaborate with DM and DMQL to discuss on vendor/data types associated with trial based on Veeva vendor tracker. 2. Create DTS and DTA based on vendor tracker, by using P21 standards. 3. Create appropriate DS requests for missing standards. 4. Perform import review for each test transfer, and production transfer for initial and during milestone. 5 5. Perform changes as required based on new requirements/protocol amendments. 6. Perform eCOA device UAT, and UAT test script creation. 7. Perform Key mappings/unblinding rules as required. 8. Adhere to good documentation practice, and follow the process for required review/approval in ETMF. Preferred Candidate: Must h...

Role & responsibilities : Core responsibilities: 1. Collaborate with DM and DMQL to discuss on vendor/data types associated with trial based on Veeva vendor tracker. 2. Create DTS and DTA based on vendor tracker, by using P21 standards. 3. Create appropriate DS requests for missing standards. 4. Perform import review for each test transfer, and production transfer for initial and during milestone. 5 5. Perform changes as required based on new requirements/protocol amendments. 6. Perform eCOA device UAT, and UAT test script creation. 7. Perform Key mappings/unblinding rules as required. 8. Adhere to good documentation practice, and follow the process for required review/approval in ETMF. Pref...

Roles and Responsibility Analyze and interpret complex clinical trial data to identify trends and patterns. Develop and maintain databases and systems for managing clinical trial data. Collaborate with cross-functional teams to ensure accurate and timely delivery of data. Conduct quality control checks on data to ensure accuracy and integrity. Provide insights and recommendations to stakeholders based on data analysis. Stay up-to-date with industry developments and best practices in clinical data analysis. Job Requirements Strong understanding of clinical trial design, protocols, and statistical analysis plans. Proficiency in database management systems such as SQL or Oracle. Experience with...

Roles and Responsibility Conduct thorough reviews of clinical trial data to ensure accuracy, completeness, and compliance with regulatory requirements. Collaborate with cross-functional teams to identify and resolve data discrepancies and issues. Develop and maintain detailed reports of findings and recommendations for data improvements. Participate in developing and implementing process improvements to enhance data quality and efficiency. Provide training and support to junior staff members on data review procedures and best practices. Stay up-to-date with changing regulations and guidelines related to clinical data management. Job Requirements Strong understanding of clinical data manageme...

JR135624 CRA I /II 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 Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate 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 innovative treatments and therapies. What you will be doing Conducting site qualification, initiation, monitoring, and close-out visit...

ZS Life Science R&D Technologist in Clinical development ZS life science R&D team partners with clients to discover and develop innovative medicines that improve patient's lives. Our work spans consulting, analytics and technology (services and platforms) projects across the several domains. We have 3500+ zs professionals that deliver R&D programs, $100MM+ invested in R&D data, analytics and technology assets and 100+ clients on R&D programs. Our Clinical/Drug Development division displays a substantial history of contributing to numerous client projects with significant results in drug development. The Drug Development R&D Technologists possess a deep understanding of technological solution...

What Youll Do - You will design & implement various innovative solutions in the realms of clinical trial, data management, analytics You will work in designing common data model based on clinical standards like SDTM / ADAM/ I ISS/ ISE . You will work on designing safety data mart for cross study analysis and exploratory analysis You will work on building analysis ready datasets which serves various safety and exploratory use cases across clinical trials. You have experience of building usecases like safety signal detection, reverse translation research, combination therapy exploration As a solution lead, your role will involve planning, offering tech consultancy, conducting assessments,and e...

Analyze and interpret complex clinical data using SAS. Develop and maintain databases, data systems, and computer models for clinical trial management. Collaborate with cross-functional teams to design and implement data analysis plans. Ensure data quality, integrity, and compliance with regulatory requirements. Provide technical support and training to junior staff members on data analysis tools and techniques. Participate in project meetings and contribute to the development of project plans and timelines. Job Requirements Strong knowledge of SAS programming language and its applications in clinical data analysis. Experience with Veeva or similar clinical trial management systems. Excellen...

Design, develop, and implement clinical trial data management systems using SAS. Collaborate with cross-functional teams to ensure seamless integration of clinical data into existing systems. Develop and maintain complex SQL queries to extract insights from large datasets. Troubleshoot issues related to clinical trial data management and reporting. Ensure compliance with regulatory requirements and industry standards. Participate in code reviews and contribute to improving overall code quality. Job Requirements Strong proficiency in SAS programming language, including Base SAS and Enterprise Guide. Experience with SQL programming, particularly in a clinical trial context. Knowledge of clinic...

Manage and resolve discrepancies in clinical trial data. Develop and implement effective data reconciliation processes. Collaborate with cross-functional teams to ensure accurate and timely resolution of data issues. Analyze and report on data trends and patterns to identify areas for improvement. Ensure compliance with regulatory requirements and industry standards. Provide training and support to junior team members on data reconciliation best practices. Job Requirements Strong understanding of clinical trial data management principles and practices. Experience with data reconciliation tools and technologies. Excellent analytical and problem-solving skills. Ability to work effectively in a...