300 Cdm Jobs - Page 2

Manage and oversee the development, implementation, and maintenance of clinical data management systems. Collaborate with cross-functional teams to ensure accurate and timely delivery of clinical data. Required Candidate profile Strong knowledge of Veeva EDC system and its applications in clinical trials. Experience in managing clinical data from various sources, including electronic health records and laboratory results.

Design, develop, and implement Veeva EDC clinical programming solutions for clients. Collaborate with cross-functional teams to ensure seamless integration of Veeva EDC ystems. Required Candidate profile Strong understanding of Veeva EDC principles and technologies. Experience with clinical trial data management systems. Excellent problem-solving skills and attention to detail.

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...

SAP SuccessFactors Recruiting & Onboarding Consultant(ONB 2.0, ONB 1.0) Active Certification in Success Factors ONB 2.0 Recruitment, ONB1.0 At least 2 End to End Implementation in Recruitment module Hands on experience in Creation of Panels. Hands on experience in working with Security Roles. Should have worked in Notifications, Rules. Document Centre. Experience in User roles and Admin Roles, RBP roles and Proficient Knowledge in Onboarding XMLs. Integration knowledge in RCM ONB - EC. Working knowledge on Adhoc Reports. Hands on Experience in Forms. Hands on Experience in Scheduling Jobs and Managing Jobs. Expertise in end to end Recruitment management process that include Requisition manag...

SAP SuccessFactors Recruiting & Onboarding Consultant(ONB 2.0, ONB 1.0) Active Certification in Success Factors ONB 2.0 Recruitment, ONB1.0 At least 2 End to End Implementation in Recruitment module Hands on experience in Creation of Panels. Hands on experience in working with Security Roles. Should have worked in Notifications, Rules. Document Centre. Experience in User roles and Admin Roles, RBP roles and Proficient Knowledge in Onboarding XMLs. Integration knowledge in RCM ONB - EC. Working knowledge on Adhoc Reports. Hands on Experience in Forms. Hands on Experience in Scheduling Jobs and Managing Jobs. Expertise in end to end Recruitment management process that include Requisition manag...

where youll be supported and inspired by a collaborative community of colleagues around the world, where youll be supported and inspired by a collaborative community of colleagues around the world, and where you ll be able to reimagine what s possible. Join us and help the world s leading organizations unlock the value of technology and build a more sustainable, more inclusive world. Your Role Experience 5 to 7 years Location Pune/ Bangalore Must have skillsTIBCO products (EMS7.x / 8.x, BW 5.x/6.x, Active Spaces, APIX, Adapters /SDK) . Shift timings 10am to 7pm IST Detailed JD Minimum 5 to 7 years of hands-on experience as a SOA/Integration software engineer with proven hands on design AND d...

• Provide training On End To End TMF Process • Process TMF documents with good documentation practices, indexing requirements, and TMF readiness criteria. • 3–5 years of experience in TMF management, clinical documentation, or records management. Required Candidate profile • Hands-on experience with eTMF systems and Softwares. • Able To Give Hands-on expertise with leading eTMF systems. • Interested Directly Contact Sneha - 9133469786

About The Role Skill required: Clinical Data Services - Clinical Database Programming Designation: Clinical Data Svs Specialist Qualifications: BE/BTech/BSc Years of Experience: 7 to 11 years Language - Ability: English(Domestic) - Intermediate 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...

Responsibilities: * Manage clinical data from study start to closeout using RAVE software. * Collaborate with cross-functional teams on EDC setup and maintenance.

Responsibilities: Manage clinical trial data from start to finish using CDM software. Collaborate with cross-functional teams on study setup, data cleaning, and reporting.

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...

About The Role Skill required: Clinical Data Services - Clinical Database Programming Designation: Clinical Data Svs Specialist Qualifications: BE Years of Experience: 7 to 11 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 converging around the pat...

Role & responsibilities Job Overview Manage end-to-end delivery of data management services for single/multi-service projects with minimal guidance, ensuring quality deliverables on time and within budget, to customer satisfaction. Provide comprehensive data management expertise to Data Management (DM) team to provide high quality data management products that meet customer needs. Provide leadership to the team in the areas of project planning, execution, and close-out; Overview of financial management for data management activities; communications; and milestone deliverables. Perform role of Data Team Lead (DTL). Essential Functions • Gather Study Set up requirements through discussion and ...

About The Role Skill required: Clinical Data Services - Clinical Reports Management Designation: Clinical Data Svs Analyst Qualifications: Any Graduation Years of Experience: 3-5 Yrs 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 converging around the pa...

Provide expert support and functional and technical knowledge to ensure the scientific integrity/validity for clinical development, early development, and/or research projects Participate in the full lifecycle of producing key data and/or reports in support of data review reporting development including evaluation of requirements, design specifications, interface to programmers, report programming, coordinate validation and rollout activities along with providing quantitative analytical support Provide statistical support for regulatory submissions including planning, analysis and reporting of clinical safety and efficacy summaries May also provide statistical support to research or other R&...

Provide expert support and functional and technical knowledge to ensure the scientific integrity/validity for clinical development, early development, and/or research projects Participate in the full lifecycle of producing key data and/or reports in support of data review reporting development including evaluation of requirements, design specifications, interface to programmers, report programming, coordinate validation and rollout activities along with providing quantitative analytical support Provide statistical support for regulatory submissions including planning, analysis and reporting of clinical safety and efficacy summaries May also provide statistical support to research or other R&...

About The Role Skill required: Clinical Data Services - Clinical Reports Management Designation: Clinical Data Svs Analyst Qualifications: BE/BTech/BSc Years of Experience: 3 to 5 years Language - Ability: English(Domestic) - Intermediate 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 enabl...

About The Role Skill required: Clinical Data Services - Clinical EDC Build Designation: Clinical Data Svs Associate Qualifications: BE/BTech Years of Experience: 1 to 3 years What would you do? You will be part of our Life Sciences R&D division, which offers a comprehensive range of services across the life sciences sector. This includes Clinical Data Management, regulatory services, pharmacovigilance, and patient services solutions. Employees within this clinical capability will join one of our sub-offerings, such as Clinical Database build and Clinical Reporting. In these roles, you will support leading biopharma companies in realizing their vision, enhancing outcomes by focusing on the pa...

About The Role Skill required: Clinical Data Services - Clinical EDC Build Designation: Clinical Data Svs Associate Qualifications: BE/BTech Years of Experience: 1 to 3 years What would you do? You will be part of our Life Sciences R&D division, which offers a comprehensive range of services across the life sciences sector. This includes Clinical Data Management, regulatory services, pharmacovigilance, and patient services solutions. Employees within this clinical capability will join one of our sub-offerings, such as Clinical Database build and Clinical Reporting. In these roles, you will support leading biopharma companies in realizing their vision, enhancing outcomes by focusing on the pa...

About The Role Skill required: Clinical Data Services - Clinical EDC Build Designation: Clinical Data Svs Associate Qualifications: BE/BTech Years of Experience: 1 to 3 years What would you do? You will be part of our Life Sciences R&D division, which offers a comprehensive range of services across the life sciences sector. This includes Clinical Data Management, regulatory services, pharmacovigilance, and patient services solutions. Employees within this clinical capability will join one of our sub-offerings, such as Clinical Database build and Clinical Reporting. In these roles, you will support leading biopharma companies in realizing their vision, enhancing outcomes by focusing on the pa...

About The Role Skill required: Clinical Data Services - Clinical EDC Build Designation: Clinical Data Svs Associate Qualifications: BE/BTech Years of Experience: 1 to 3 years What would you do? You will be part of our Life Sciences R&D division, which offers a comprehensive range of services across the life sciences sector. This includes Clinical Data Management, regulatory services, pharmacovigilance, and patient services solutions. Employees within this clinical capability will join one of our sub-offerings, such as Clinical Database build and Clinical Reporting. In these roles, you will support leading biopharma companies in realizing their vision, enhancing outcomes by focusing on the pa...

About The Role Skill required: Clinical Data Services - Clinical EDC Build Designation: Clinical Data Svs Associate Qualifications: BE/BTech Years of Experience: 1 to 3 years What would you do? You will be part of our Life Sciences R&D division, which offers a comprehensive range of services across the life sciences sector. This includes Clinical Data Management, regulatory services, pharmacovigilance, and patient services solutions. Employees within this clinical capability will join one of our sub-offerings, such as Clinical Database build and Clinical Reporting. In these roles, you will support leading biopharma companies in realizing their vision, enhancing outcomes by focusing on the pa...

As an Oracle Customer Data Management techno-functional consultant - CX at Strategic Resources International, your role will involve the implementation, integration, and support of the Customer Data Management module in Oracle Cloud Applications. You will be responsible for: - Demonstrating excellent techno-functional knowledge and hands-on experience with Oracle Customer Data Management (CDM) tools and technologies. - Leading at least 2 Oracle CDM implementations as a techno-functional consultant. - Creating and modifying data structures, views, and data stores in Oracle CDM. - Handling ad-hoc data change requests from clients effectively. - Working with complex data structures to extract a...

About The Role Skill required: Clinical Data Operations - Clinical Database Testing Designation: Clinical Data Svs Analyst Qualifications: Master Degree in Life Sciences Years of Experience: 3 to 5 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 ...

Role & responsibilities Job Summary (Clinical Trial Team Leader) Oversees and manages clinical trial execution. Ensures compliance with regulatory standards, timelines, and quality metrics. Provides cross-functional leadership and strategic planning. Supervises study teams to deliver successful trial outcomes. Key Responsibilities Lead cross-functional teams (ops managers, team leads, quality analysts, support staff). Mentor team members; promote accountability and continuous improvement. Monitor performance; address risks, issues, and deviations. Manage client onboarding, workflows, quality assurance, and process optimization. Deliver operational reports and performance updates to senior ma...