Clinical Data Programming
4 weeks ago
Job Description Job Purpose - The incumbent manages Clinical Data Programming to ensure timely creation, validation, testing, implementation and maintenance of databases required across all assigned projects. - Analyzes study protocol and project requirement(s), identifies data quality rules, and design data entry interfaces in accordance to the study Protocol, DMP, SOP and all applicable regulatory requirements and standards. Key Roles And Responsibilities - Deploy complete, accurate, and efficient clinical study databases to support Data Management and data processing activities. - Facilitate the preparation, transfer, and integration of clinical data from internal and external sources into study databases. Deliver clinical study data in various formats to key stakeholders as needed. - Ensure high-quality deliverables and foster strong collaboration with internal and external stakeholders. Actively participate in project teams to develop and maintain programs aligned with project standards. - Manage data exchange with external stakeholders (e.g., labs, ECG vendors, Safety/IDMCs) as required. - Provide ongoing end-user support to project teams to ensure systems and programs function correctly and efficiently. - Set up and support data review and reporting tools for DM stakeholders, including SAS programmers, Clinical, Medical, Pharmacovigilance, and Regulatory Affairs, and the Study Management Team. - Offer technical expertise and programming support to projects and data management staff. - Communicate project status and key issues to DM Management. - Contribute to the development of new data systems programming procedures and processes. - Stay current with technological advancements and collaborate with Global Training and IT teams to maximize their application in data management. - Mentor and train team members while assisting in work delegation. - Support and maintain standardization of CRF/eCRF modules, data quality rules, data structures, libraries, code lists, and dictionaries in line with CDISC standards. - Participate in evaluating external vendors and technologies for alignment with project goals and quality standards. - Identify opportunities for process improvement through standardization and technology to enhance efficiency, quality, and timeliness of deliverables. Advanced Analytics & Visualization Responsibilities - Strong proficiency in Power BI, R, and/or SAS for programming data listings, KRI visuals, and developing impactful visualizations that aid cross-functional teams (e.g., Medical Monitors, Biostatisticians) in drawing meaningful inferences. - Ability to build analytical models, generate reports, and design dashboards tailored to business requirements. - Experience in working with dashboards integrating multiple data sources (Excel, TXT, Oracle, SAS) using tools like Power BI and SAS. - Develop listings and respond to ad-hoc requests by producing tables based on supplied shells, and support edit checks, patient profiles, protocol deviations, coding reports, and other data analysis requirements. Qualification, Skill And Competencies Requirements - Preferably a minimum of a Bachelor's degree in a Life Science, Computer Science or related discipline. - Minimum 8-10 years of clinical data programming experience including working knowledge using clinical data programming tools and applications. - Experience of leading clinical programming effort across global clinical studies is preferred. Job Location Gurugram, HR Reporting To Clinical Database Programming Lead (CDPL)
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Clinical Trial Physician
2 weeks ago
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Senior Data Analysis
7 days ago
India Advanced Clinical Full timeThe Senior Biostatistician is responsible for leading, developing, implementing, and overseeing statistical strategies and deliverables in support of the Client’s R&D sponsored clinical trials. Under the guidance of Head of Biostatistics, this role contributes to the planning, execution and interpretation of statistical analyses across development...
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Clinical Database Programmer
4 weeks ago
Gurugram, Gurugram, India SUN PHARMA Full timeJob Description Qualification, Skill and Competencies Requirements - Preferably a minimum of a Bachelor's degree in a Life Science, Computer Science or related discipline. - Minimum 8-10 years of clinical data programming experience including working knowledge using clinical data programming tools and applications. - Experience of leading clinical...
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Clinical Research Associate
4 weeks ago
Bengaluru, Karnataka, India, Karnataka MS CLINICAL RESEARCH Full timeJob Title: Clinical Research Associate (CRA)Company: MS Clinical Research Pvt LtdExperience: Minimum 3 yearsAbout 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...
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Clinical Data Associate
5 days ago
India Novotech Full time ₹ 2,00,000 - ₹ 4,00,000 per yearAbout the RoleThe Clinical Data Associate supports the day-to-day operations of the data management projects, providing in-house data entry support to projects and administrative support to CDMsResponsibilities:Data entry of clinical trial data using Clinical Data Management software.Assistance in review of data queries to be raised with sponsor...
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Senior Manager, Clinical Programming
4 weeks ago
Bengaluru, India eClinical Solutions Full timeJob Description The Senior Manager, Clinical Programming is responsible for strategic oversight, implementation, and support of clinical systems and the associated operational use of these systems as part of client engagements within the Data Services business unit. The Senior Manager, Clinical Programming will provide direction and manage staff associated...
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Clinical Data Associate
2 weeks ago
India Novotech Full time**About the role**: Supports the day-to-day operations of the data management projects, providing in-house data entry support to projects and administrative support to CDMs, according to GCDMP guidelines, local regulatory requirements and Novotech/Client SOPs. **Minimum Qualifications & Experience**: Graduate in a clinical or life sciences related field....
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Senior Clinical Research Associate
2 weeks ago
Bengaluru, Karnataka, India, Karnataka MS CLINICAL RESEARCH Full timeJob Title: Senior Clinical Research Associate (Sr. CRA)Company: MS Clinical Research Pvt LtdExperience: Minimum 5 yearsAbout UsMS Clinical Research (MSCR) is a leading clinical research organization committed to advancing scientific innovation and improving healthcare outcomes. We conduct high-quality clinical trials that adhere to global standards of...
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Clinical Data Associate Ii
1 week ago
India Novotech Full time**Brief Position Description**: Supports the day-to-day operations of the data management projects, providing in-house data entry support to projects and administrative support to CDMs, according to GCDMP guidelines, local regulatory requirements and Novotech/Client SOPs. **Minimum Qualifications & Experience**: Graduate in a clinical or life sciences...
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Clinical Data Associate
4 weeks ago
India Novo Tech Full timeJob Description JOB DESCRIPTION About the role: Supports the day-to-day operations of the data management projects, providing in-house data entry support to projects and administrative support to CDMs, according to GCDMP guidelines, local regulatory requirements and Novotech/Client SOPs. Minimum Qualifications & Experience: Graduate in a clinical or...
