69 Clinical Programming Jobs - Page 2

Roles and Responsibility 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. Provide training and support to clients on the use of Veeva EDC clinical programming tools. Participate in the development of best practices and standards for Veeva EDC clinical programming. Job Requirements Strong understanding of Veeva EDC clinical programming principles and methodologies. Experience working with var...

Roles and Responsibility 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. Provide training and support to clients on the use of Veeva EDC clinical programming tools. Stay up-to-date with industry trends and emerging technologies in Veeva EDC clinical programming. Job Requirements Strong knowledge of Veeva EDC clinical programming principles and practices. Experience working with IT Service &...

Roles and Responsibility Design, develop, and implement clinical trial data management systems using Veeva EDC. Collaborate with cross-functional teams to ensure seamless integration of clinical data into the development process. Develop and maintain high-quality, accurate, and timely clinical trial data. Troubleshoot and resolve issues related to clinical data management and reporting. Ensure compliance with regulatory requirements and industry standards. Participate in project planning, execution, and delivery to meet business objectives. Job Requirements Strong knowledge of Veeva EDC and its applications in clinical trials. Experience working in the IT Service & Consulting industry, prefe...

We are looking for a highly skilled and experienced Clinical Data Analyst and Programmer with expertise in SAS and Veeva to join our team at Gratitude India Manpower Consultants Pvt. Ltd. The ideal candidate will have 2-5 years of experience in the IT Service & Consulting industry. Roles and Responsibility Analyze and interpret complex clinical trial data using SAS. Develop and maintain databases, tables, and reports using Veeva. Collaborate with cross-functional teams to ensure accurate and timely delivery of projects. Design and implement data visualization tools to communicate insights to stakeholders. Ensure compliance with regulatory requirements and company standards. Provide technical...

We are looking for a highly skilled and experienced Clinical Data Analyst and Programmer with expertise in SAS and Veeva to join our team at Gratitude India Manpower Consultants Pvt. Ltd. The ideal candidate will have a strong background in the IT Service & Consulting industry, specifically in clinical data analysis and programming using SAS and Veeva. Roles and Responsibility Develop and maintain complex databases and systems for clinical trial data management. Design, develop, and implement data models, data flows, and validation rules for clinical trial data. Collaborate with cross-functional teams to ensure accurate and timely delivery of high-quality results. Troubleshoot and resolve te...

Looking for a skilled Clinical Data Analyst and Programmer with expertise in SAS and Veeva to join our team. The ideal candidate will have 3-8 years of experience in the field. Roles and Responsibility Analyze and interpret complex clinical trial data using SAS. Develop and maintain databases, tables, and reports using Veeva. Collaborate with cross-functional teams to ensure accurate and timely delivery of results. Design and implement effective data management strategies. Ensure compliance with regulatory requirements and company standards. Provide technical support and training to junior team members. Job Requirements Strong knowledge of SAS programming language and its applications in cli...

Roles and Responsibility Design, develop, and implement clinical trial protocols using SAS. Collaborate with cross-functional teams to ensure timely delivery of high-quality deliverables. Develop and maintain complex statistical analysis plans and datasets. Troubleshoot and resolve technical issues related to clinical trial data management. Participate in project meetings and provide input on project scope and timelines. Ensure compliance with regulatory requirements and company standards. Job Requirements Strong knowledge of clinical trial design, protocol development, and statistical analysis. Proficiency in SAS programming language, including Base SAS and Enterprise Guide. Experience with...

Roles and Responsibility Design, develop, and implement clinical trial protocols using SAS. Collaborate with cross-functional teams to ensure timely delivery of high-quality deliverables. Develop and maintain complex statistical analysis plans and datasets. Troubleshoot and resolve technical issues related to clinical trial data management systems. Participate in project meetings and provide input on project scope and timelines. Ensure compliance with regulatory requirements and company standards. Job Requirements Strong knowledge of clinical trial design principles and methodologies. Proficiency in SAS programming language, including Base SAS, Enterprise Guide, and Macros. Experience workin...

Roles and Responsibility Design, develop, and implement clinical trial protocols using SAS. Collaborate with cross-functional teams to ensure timely delivery of high-quality deliverables. Develop and maintain complex statistical analysis plans and datasets. Troubleshoot and resolve technical issues related to clinical trial data management. Participate in project meetings and provide input on project scope and timelines. Ensure compliance with regulatory requirements and company standards. Job Requirements Strong knowledge of clinical trial design, protocol development, and statistical analysis. Proficiency in SAS programming language, including Base SAS and Proc SQL. Experience with clinica...

Roles and Responsibility Design, develop, and implement clinical data programming solutions using R/SQL. Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Develop and maintain complex databases and data systems. Troubleshoot and resolve technical issues related to clinical data programming. Ensure compliance with regulatory requirements and industry standards. Participate in code reviews and contribute to improving overall code quality. Job Requirements Strong knowledge of R/SQL programming languages. Experience working with large datasets and complex data systems. Excellent problem-solving skills and attention to detail. Ability to work collaborative...

Roles and Responsibility Design, develop, and implement clinical data programming solutions using R/SQL. Collaborate with cross-functional teams to ensure accurate and timely delivery of projects. Develop and maintain complex databases and data systems. Write efficient and well-documented code. Troubleshoot and resolve technical issues related to clinical data programming. Participate in code reviews and contribute to improving overall code quality. Job Requirements Strong knowledge of R/SQL and its applications in clinical data programming. Experience working with large datasets and developing scalable solutions. Excellent problem-solving skills and attention to detail. Ability to work coll...

Roles and Responsibility Design, develop, and implement clinical trial data management systems using SAS and SQL. Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Develop and maintain complex statistical analysis plans and reports. Troubleshoot and resolve technical issues related to clinical trial data management. Ensure compliance with regulatory requirements and industry standards. Participate in project planning, execution, and monitoring activities. Job Requirements Strong knowledge of IT Service & Consulting, particularly in clinical programming using SAS and SQL. Experience working on clinical trials and data management projects. Excellent pro...

Roles and Responsibility Design, develop, and maintain clinical databases using R/SQL. Collaborate with cross-functional teams to ensure data quality and integrity. Develop and implement data validation and verification processes. Troubleshoot and resolve data-related issues efficiently. Ensure compliance with regulatory requirements and industry standards. Participate in the development of new systems and technologies. Job Requirements Strong knowledge of R/SQL and clinical data programming principles. Experience working with large datasets and complex data structures. Excellent problem-solving skills and attention to detail. Ability to work collaboratively in a team environment. Strong com...

As a Statistical Programming Manager at Medpace, based in Mumbai, India, within the Biostatistics team, you will have a crucial role in supporting project teams on programming matters. Your responsibilities will include managing programming staff, ensuring high-quality delivery, providing leadership and training for the Programming group, and leading the development of Programming standards to maximize efficiencies. Key Responsibilities: - Support project teams on programming matters - Manage programming staff - Ensure high-quality delivery - Provide leadership and training for the Programming group - Lead the development of Programming standards to maximize efficiencies Qualifications Requi...

Role Overview: As an Elluminate Data Programmer, you will be responsible for developing, maintaining, and delivering high-quality clinical data programs and visualizations using Elluminate. You will work closely with cross-functional clinical teams to ensure accurate and insightful reporting that supports clinical trial operations, data cleaning, and regulatory compliance Core Responsibilities: Create and manage clinical reports, dashboards, and visualizations. Write SQL queries to extract and transform clinical data. Collaborate with clinical teams to meet reporting needs. Ensure compliance with CDISC, SDTM, and GCP standards. Support data quality checks and documentation Technical Expertis...

The R&D Programmer III position at Teva Pharmaceuticals in Bangalore, India offers an exciting opportunity for a Senior Clinical Programmer to support clinical projects and regulatory submissions. As part of a global team dedicated to making good health more affordable and accessible, you will play a lead role in generating and validating analysis datasets, tables, listings, and figures. Your expertise in SAS programming will be crucial in developing global data standards, including SDTM, ADaM, and Teva's database structure. Your responsibilities will include working at the project level, providing input for budget planning, delivering assignments with quality and within timelines, overseein...

We are seeking a proactive Principal Clinical Programmer to serve as a subject matter expert and technical leader for clinical programming projects. The ideal candidate will have extensive experience with Medidata Rave and Custom Functions and will be responsible for leading project teams, managing deliverables, and mentoring junior programmers. Roles and Responsibilities Act as a subject matter expert on core business packages, including Medidata, Rave, Oracle OC/RDC, Oracle Inform, and SAS . Utilize development tools to design, write, validate, and maintain software to meet specifications. Generate and maintain all required documentation, including specifications, coding, and validation ef...

We are seeking a proactive Principal Clinical Programmer to serve as a subject matter expert and technical leader for clinical programming projects. The ideal candidate will have extensive experience with Medidata Rave and Custom Functions and will be responsible for leading project teams, managing deliverables, and mentoring junior programmers. Roles and Responsibilities Act as a subject matter expert on core business packages, including Medidata, Rave, Oracle OC/RDC, Oracle Inform, and SAS . Utilize development tools to design, write, validate, and maintain software to meet specifications. Generate and maintain all required documentation, including specifications, coding, and validation ef...

We are seeking a proactive Principal Clinical Programmer to serve as a subject matter expert and technical leader for clinical programming projects. The ideal candidate will have extensive experience with Medidata Rave and Custom Functions and will be responsible for leading project teams, managing deliverables, and mentoring junior programmers. Roles and Responsibilities Act as a subject matter expert on core business packages, including Medidata, Rave, Oracle OC/RDC, Oracle Inform, and SAS . Utilize development tools to design, write, validate, and maintain software to meet specifications. Generate and maintain all required documentation, including specifications, coding, and validation ef...

We are seeking a Principal Clinical Programmer (Rave/Veeva) to be a subject matter expert and lead developer for our core business packages. This pivotal role involves providing technical support, leading programming projects, and mentoring a team to accelerate the delivery of clinical therapies. Roles and Responsibilities Act as a subject matter expert and provide technical support for core business packages such as Medidata, Rave, Oracle OC/RDC, and Veeva . Design, write, validate, and maintain software to meet project specifications in a timely and productive manner. Generate and maintain all required documentation, including specifications and validation efforts for eCRFs, database creat...

We are seeking a Principal Clinical Programmer (Rave/Veeva) to be a subject matter expert and lead developer for our core business packages. This pivotal role involves providing technical support, leading programming projects, and mentoring a team to accelerate the delivery of clinical therapies. Roles and Responsibilities Act as a subject matter expert and provide technical support for core business packages such as Medidata, Rave, Oracle OC/RDC, and Veeva . Design, write, validate, and maintain software to meet project specifications in a timely and productive manner. Generate and maintain all required documentation, including specifications and validation efforts for eCRFs, database creat...

The Statistical Programming Manager position is a full-time opportunity based in Mumbai, India, within the Biostatistics team. As a Statistical Programming Manager, you will play a crucial role in supporting project teams on programming matters, managing programming staff, ensuring high-quality delivery, providing leadership and training for the Programming group, and leading the development of Programming standards to maximize efficiencies. To qualify for this role, you should hold a Bachelor/Master's degree in statistics, mathematics, health informatics, computer science, or a related field. Additionally, you should have proficiency in SAS programming skills, at least 5 years of clinical p...

At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. We are looking for a Senior Clinical Data Manager I to join our A-team (hybrid*). The Senior Clinical Data Manager I (SrCDM1) is responsible for leading data management activities of the Allucent Data Management (DM) department. In this role, you will manage, coordinate, review, and approve DM deliverables from database design & set-up, through cleaning and reporting to database locking. It is crucial to ensure that the completeness, accuracy, and consistency of clinical data meet the...

The company's corporate activities are expanding rapidly, and we are currently in search of a full-time Statistical Programming Manager to join our Biostatistics team in India, Mumbai. In this role, you will collaborate with a team to complete tasks and projects crucial to the company's success. If you are seeking a dynamic career where you can utilize your existing skills and further advance your professional development, this opportunity is ideal for you. As the Statistical Programming Manager, your responsibilities will include providing support to project teams on programming issues, overseeing programming staff, coordinating task assignments, and reviewing activities to ensure high-qual...

At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. We are looking for a Senior Clinical Data Manager I to join our A-team in the Chennai location. The Senior Clinical Data Manager I (SrCDM1) will be responsible for leading data management activities of the Allucent Data Management (DM) department. In this role, your key tasks will include leading and serving as the primary contact for DM with all relevant parties both internally and externally, planning and projecting the resources required, monitoring tasks against budgets and foreca...