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25.0 - 30.0 years

25 - 30 Lacs

hyderabad

Work from Office

What you will do The Associate Vice President, Clinical Data Management is a member of the Global Development Operations (GDO) leadership team and is a strategic partner to the R&D organization. The AVP will lead Amgens Clinical Data Management function within GDO, ensuring the highest quality of clinical data collection, processing, and analysis to support regulatory submissions and clinical development programs. This role is responsible for the strategic direction, leadership, and operational oversight of data management processes supporting clinical trials across all therapeutic areas and phases. This AVP will collaborate closely with cross-functional teams including clinical operations, ...

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4.0 - 9.0 years

6 - 10 Lacs

pune, bengaluru

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Job Summary: Synechron is seeking a highly skilled and experienced VisionPLUS MBS SME/Developer to join our dynamic team. The ideal candidate will have a proven track record of working on multiple MBS projects, demonstrating deep expertise in VisionPLUS MBS systems, and providing innovative solutions to complex banking and financial services challenges. Required: VisionPLUS Modules (MBS) with substantial hands-on experience Mainframe Technologies: JCL, COBOL, VSAM, CICS Development methodologies: Agile (Scrum/Kanban) or Waterfall Preferred: Vision Flex framework Experience with Batch Processing systems and subsystems Version control tools (e.g., Git, Rational Team Concert) Knowledge of cloud...

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2.0 - 6.0 years

3 - 4 Lacs

navi mumbai

Work from Office

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

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0.0 - 3.0 years

5 - 6 Lacs

hyderabad, chennai, bengaluru

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

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5.0 - 7.0 years

0 Lacs

bengaluru, karnataka, india

On-site

We are looking for a Mechanical Engineer to provide technical mechanical engineering support, ensuring that projects are delivered to high standards and within agreed timelines. Your Purpose As a Mechanical Engineer, you'll play a key role in the design and delivery of mechanical systems, collaborating with multidisciplinary teams to ensure project success. You'll focus on developing innovative solutions for water and wastewater treatment processes, while maintaining a commitment to health, safety, and operational excellence. What You'll Be Doing Design mechanical and hydraulic systems for water treatment plant processes, ensuring compliance with statutory and company standards. Lead the des...

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5.0 - 10.0 years

19 - 25 Lacs

gurugram, bengaluru

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Lead and manage the technical and commercial delivery of Rail Electric Track Equipment- ETE (Third Rail) projects, with a primary focus on rail Switch & Crossing (S&C) Renewal Works. Design of Positive Feeders and Negative Returns, including traction substation cabling, conductor rail layouts, negative bonding, hook switches, track isolating switches, Cable Routes and Cable Management Sleeper (CMS) systems in line with client specifications. Prepare key elements of design deliverables including technical reports, electrical calculations and CAD drawings in industry standard software.Act as Lead Engineer or Contractors Responsible Engineer (CRE), checker ensuring compliance with client requir...

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5.0 - 10.0 years

15 - 30 Lacs

hyderabad

Work from Office

Responsibilities: Lead and manage a team of QA professionals across the globe, including manual testers and automation engineers. Actively collaborate with cross functional teams including Business System Analysts, Developers, Project/Deliver Mgmt. Teams, and Product Managers to ensure quality throughout the development lifecycle. Embed the QA team early on in projects where we can work hand in hand with the BSA team during the data discovery process to build out well executed use cases. Provide feedback to the team on product quality, call out risks/issues, and balance quality with time bound delivery with a release perspective. Document and maintain manual as well as automated test result....

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7.0 - 11.0 years

3 - 7 Lacs

bengaluru

Work from Office

Skill required: Clinical Data Services - Clinical Reports Management Designation: Clinical Data Svs Specialist Qualifications: BE/BTech/MCA Years of Experience: 7 to 11 years About Accenture 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 worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. Visit us at www.accenture.com What would you do You will be aligned with our Life Sciences R&D vertica...

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1.0 - 3.0 years

2 - 6 Lacs

bengaluru

Work from Office

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...

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1.0 - 3.0 years

2 - 6 Lacs

bengaluru

Work from Office

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...

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3.0 - 6.0 years

4 - 8 Lacs

hyderabad

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Looking for a skilled Functional Tester to join our team in Hyderabad. The ideal candidate will have 3-6 years of experience in functional testing, preferably in the cards domain. Roles and Responsibility Develop and execute comprehensive test plans to ensure high-quality software delivery. Collaborate with cross-functional teams to identify and prioritize testing requirements. Design and implement automated testing scripts using Python. Analyze and report defects found during testing, working closely with development teams to resolve issues. Participate in agile development methodologies, providing feedback and suggestions for process improvements. Stay up-to-date with industry trends and e...

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7.0 - 10.0 years

7 - 10 Lacs

bengaluru

Work from Office

Requisite work experience, certification and skill set: Proven experience managing construction and/or engineering projects valued at 5m+. Strong organizational and multitasking skills, with a keen attention to detail. Excellent interpersonal skills, with the ability to effectively communicate with clients, contractors, and project teams. Strong commercial awareness and a focus on achieving project objectives within budget and scope. A recognized project management qualification or certification (e. g. , APM, Chartered status) is essential. IOSH Managing Safely qualifications and experience with CDM regulations is required. Proficiency in Primavera P6, Microsoft Project, Excel, Word, and Acc...

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10.0 - 15.0 years

10 - 14 Lacs

bengaluru

Work from Office

We focus on gaining, refining and sharing expertise in the energy and utility sector, then provide strategic advice and implement outcome-driven solutions. Working with customers across the utility value chain, we deliver sustainable and lasting improvements to their efficiency and performance, adding value to their bottom line. Demand for power, gas and water is consistently growing as the population of the planet expands. Our goal is to support large consumers of energy and water, and improve the sustainability of resources by increasing efficiency and optimizing existing operations. We also develop commercially successful ways to use renewable resources which deliver transformative advant...

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5.0 - 7.0 years

6 - 10 Lacs

mumbai suburban

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Roles and Responsibility Manage and maintain accurate and up-to-date clinical trial data. Develop and implement effective data management plans and procedures. Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Analyze and interpret complex data sets to inform business decisions. Develop and maintain reports and dashboards to track key performance indicators. Ensure data quality and integrity by implementing robust validation and verification processes. Job Requirements Strong knowledge of clinical data management principles and practices. Experience with data analysis and interpretation tools and techniques. Excellent communication and collaboration s...

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3.0 - 4.0 years

2 - 3 Lacs

chennai

Work from Office

Responsibilities: * Collaborate with cross-functional teams on data analysis and reporting * Manage manufacturing plant data using GCP/CDM principles * Ensure compliance with industry standards and regulatory requirements

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5.0 - 10.0 years

3 - 7 Lacs

bengaluru

Work from Office

Manage and oversee clinical study data management activities, ensuring compliance with regulatory requirements. Develop and implement effective data management plans to ensure data quality and integrity. Collaborate with cross-functional teams to identify and resolve data-related issues. Conduct regular audits to ensure adherence to data management standards. Provide training and support to junior staff members on data management best practices. Ensure timely delivery of high-quality results while maintaining attention to detail. Job Requirements Strong understanding of clinical trial conduct, including GCP guidelines and regulatory requirements. Experience with data management systems, such...

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3.0 - 5.0 years

1 - 5 Lacs

bengaluru

Work from Office

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...

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3.0 - 6.0 years

3 - 7 Lacs

pune

Work from Office

Design, develop, and implement Veeva EDC clinical programming solutions for clients. Collaborate with cross-functional teams to identify and prioritize project requirements. Develop and maintain high-quality code that meets client specifications and industry standards. Troubleshoot and resolve technical issues related to Veeva EDC clinical programming. Participate in code reviews and contribute to improving overall code quality. Stay up-to-date with industry trends and emerging technologies in Veeva EDC clinical programming. Job Requirements Strong understanding of Veeva EDC clinical programming principles and practices. Proficiency in developing complex programs using Veeva EDC tools and te...

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5.0 - 8.0 years

2 - 6 Lacs

mumbai

Work from Office

Develop and maintain complex statistical models and databases for clinical trial data. Design and implement data visualization tools to effectively communicate insights to stakeholders. Collaborate with cross-functional teams to identify business needs and develop solutions. Analyze large datasets to extract meaningful trends and patterns. Develop and maintain technical documentation of data systems and processes. Provide training and support to junior team members on R and SAS programming best practices. Job Requirements Strong proficiency in R and SAS programming languages. Experience working with clinical trial data and statistical modeling techniques. Excellent analytical and problem-sol...

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2.0 - 4.0 years

6 - 10 Lacs

bengaluru

Work from Office

Manage and oversee the development and implementation of clinical data management systems. Ensure compliance with regulatory requirements and industry standards for clinical data management. Collaborate with cross-functional teams to identify and prioritize project requirements. Develop and maintain data quality control processes to ensure accuracy and integrity of clinical data. Provide training and support to staff on clinical data management systems and procedures. Analyze and resolve complex technical issues related to clinical data management. Job Requirements Strong knowledge of clinical data management principles and practices. Experience with Veeva EDC is highly desirable. Excellent ...

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5.0 - 8.0 years

2 - 6 Lacs

mumbai

Work from Office

Develop and maintain complex statistical models and databases for clinical trial data. Design and implement data visualization tools to effectively communicate insights to stakeholders. Collaborate with cross-functional teams to identify business needs and develop solutions. Conduct thorough data quality checks and ensure compliance with regulatory requirements. Provide expert-level support for data-related queries and issues. Stay up-to-date with industry trends and emerging technologies in clinical data analysis. Job Requirements Strong proficiency in R and SAS programming languages. Experience working with large datasets and complex statistical models. Excellent problem-solving skills and...

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5.0 - 8.0 years

2 - 6 Lacs

mumbai suburban

Work from Office

Develop and maintain complex statistical models and databases using R and SAS programming languages. Analyze large datasets to identify trends and patterns, providing insights to stakeholders. Design and implement data visualizations to effectively communicate results. Collaborate with cross-functional teams to integrate data into business operations. Develop and maintain technical documentation of data systems and processes. Troubleshoot and resolve issues related to data quality and integrity. Job Requirements Strong proficiency in R and SAS programming languages. Experience working with large datasets and developing complex statistical models. Excellent analytical and problem-solving skil...

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5.0 - 8.0 years

2 - 6 Lacs

navi mumbai

Work from Office

Develop and maintain complex statistical models and databases for clinical trial data. Design and implement data visualization tools to effectively communicate insights to stakeholders. Collaborate with cross-functional teams to identify business needs and develop solutions. Conduct thorough data quality checks and ensure compliance with regulatory requirements. Provide expert-level support for data-related queries and issues. Stay up-to-date with industry trends and emerging technologies in clinical data analysis. Job Requirements Strong proficiency in R and SAS programming languages. Experience working with large datasets and complex statistical models. Excellent communication and problem-...

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2.0 - 4.0 years

6 - 10 Lacs

pune

Work from Office

Roles and Responsibility Manage and oversee the development and implementation of clinical data management systems. Ensure compliance with regulatory requirements and industry standards for clinical data management. Collaborate with cross-functional teams to identify and prioritize project requirements. Develop and maintain data quality control processes to ensure accuracy and integrity of clinical data. Provide training and support to staff on clinical data management systems and procedures. Analyze and resolve complex data-related issues and discrepancies. Job Requirements Strong knowledge of clinical data management principles and practices. Experience with Veeva EDC is highly desirable. ...

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3.0 - 5.0 years

1 - 5 Lacs

pune

Work from Office

Roles and Responsibility Manage and resolve discrepancies in clinical trial data. Collaborate with cross-functional teams to ensure accurate and timely data submission. Develop and implement effective data reconciliation processes. Analyze and report on data quality metrics 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. Proficiency in data analysis and problem-solving skills. Excellent communication and interpersonal skills. Ability to work effectively in a fast...

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