75 Clinical Programming Jobs

Job Details: Manages multiple projects Likely to oversee contingent workers and/or vendors; Likely to provide training/Mentoring to others Ensures accurate set-up of data transfer processing Delivers assignments with quality and within timelines Provides strong programming support to CDISC based e-submission. Develops, debugs, and enhances SAS/SQL programs to support to support study data batch processing and oversight listings Responsible to define case report forms (CRFs) and external (non CRF) data specifications in accordancewith CDISC guideline and Teva standards Responsible to define data flow and additional startup activities related to study initiation Responsible to perform, supervi...

Role & responsibilities Medidata Patient profile (CSA) Should have experience with patient profile, preferred Medidata Patient Profile. Tool used: Medidata Clinical Data studio (new evolving tool) Good to have applicants from SAS background who have worked on patient profiles and can be further trained to our new systems. New evolving technology, Medidata CDS Reporting tool. Ability to deal effectively with sponsors and internal customers at all levels. Excellent communication and interpersonal skills, both written and spoken, with an ability to inform. Demonstrated experience in managing multiple priorities in a highly dynamic environment Experience working in a matrix-structured environmen...

Role & responsibilities Medidata Patient profile (CSA) Should have experience with patient profile, preferred Medidata Patient Profile. Tool used: Medidata Clinical Data studio (new evolving tool) Good to have applicants from SAS background who have worked on patient profiles and can be further trained to our new systems. New evolving technology, Medidata CDS Reporting tool. Ability to deal effectively with sponsors and internal customers at all levels. Excellent communication and interpersonal skills, both written and spoken, with an ability to inform. Demonstrated experience in managing multiple priorities in a highly dynamic environment Experience working in a matrix-structured environmen...

Role & responsibilities Regional Clinical Operations Manager In-Patient and Clinical Services To ensure excellence, safety, and efficiency across all inpatient areas of the Chennai Region, while driving regional clinical programs and enabling shared resource utilization for improved outcomes, productivity, and patient experience. Key Responsibilities: Operational Excellence & Patient Experience Oversee inpatient operations across wards, ICUs, HDUs, and day-care beds in all hospitals. Standardize admission, transfer, and discharge workflows for consistency and speed. Develop protocols for safe and efficient transition of care within hospital units and between facities. Drive inpatient NPS imp...

We are looking for a skilled Senior Clinical Programmer with 6 to 12 years of experience to join our team at Syneos Health, a leading player in the Pharmaceutical & Life Sciences industry. The ideal candidate will have a strong background in clinical programming and a passion for delivering high-quality results. Roles and Responsibility Develop and maintain complex clinical trial databases using various programming languages. Collaborate with cross-functional teams to design and implement clinical trial protocols. Write efficient and well-documented code that meets regulatory requirements. Troubleshoot and resolve technical issues related to clinical trial data management. Participate in pro...

Serve as the primary point of contact for system programming during study setup, collaborating with cross-functional teams. Translate clinical study reporting needs into specifications and develop custom data review solutions using tools like JReview, Spotfire, and SAS. Build and maintain global standard reports integrating CRF, biomarker, and eCOA data. Design and implement advanced SQL queries, stored procedures, and visual analytics dashboards. Contribute to SOPs, working procedures, and internal documentation to support functional excellence. Support metadata management and MDR system updates. Deliver role-based training and generate compliance and metrics reports to support clinical ope...

Role Overview: As an R&D Programmer III at Teva Pharmaceuticals, you will play a crucial role in providing high-level clinical programming support for clinical projects and regulatory submissions. Your responsibilities will include generating and validating analysis datasets, tables, listings, and figures. You will also contribute to the development of global data standards, such as SDTM, ADaM, and Teva's database structure. Additionally, you will lead departmental tasks, drive initiatives to enhance clinical programming processes, and focus on SAS Programming. Key Responsibilities: - Work at the project level and provide input for budget planning - Deliver assignments with quality and withi...

Design, develop, and implement Veeva EDC clinical programming solutions.Collaborate with cross-functional teams to ensure seamless integration of EDC systems.Develop/ maintain technical documentation for EDC systems.Troubleshoot and resolve issues Required Candidate profile Strong understanding of Veeva EDC clinical programming principles and practices.Experience working with various EDC tools and technologies.Excellent problem-solving skills and attention to detail.

Design, develop, and implement Veeva EDC clinical programming solutions.Collaborate with cross-functional teams to ensure seamless integration of EDC systems.Develop and maintain high-quality code that meets industry standards. Required Candidate profile Strong understanding of Veeva EDC clinical programming principles and practices.Experience working with various EDC systems and technologies.Excellent problem-solving skills and attention to detail.

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. Required Candidate profile 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

Design, develop, and implement Veeva EDC clinical programming solutions for clients.Collaborate with cross-functional teams to ensure seamless integration of EDC systems.Develop and maintain technical documentation for EDC systems and applications. Required Candidate profile Strong knowledge of Veeva EDC clinical programming principles and practices.Experience with EDC system implementation and maintenance.Excellent problem-solving skills and attention to detail.

Design, develop, and implement Veeva EDC clinical programming solutions.Collaborate with cross-functional teams to ensure seamless integration of EDC systems.Develop and maintain high-quality code, adhering to industry standards and best practices. Required Candidate profile Strong understanding of Veeva EDC clinical programming principles and methodologies.Proficiency in developing complex programs using Veeva EDC tools and technologies.Excellent problem-solving skills

Analyze and interpret complex clinical trial data using SAS.Develop and maintain databases, spreadsheets, and reports using Veeva.Collaborate with cross-functional teams to ensure accurate and timely delivery of results. Required Candidate profile Strong proficiency in SAS programming language.Experience with Veeva database management system.Excellent analytical and problem-solving skills.Ability to work independently and as part of a team.

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. Required Candidate profile Strong knowledge of R/SQL programming languages. Experience working with clinical data management systems. Understanding of database design principles and data modeling techniques.

Develop and maintain databases, spreadsheets, and reports for tracking and analyzing clinical trial data.Collaborate with cross-functional teams to ensure accurate and timely delivery of high-quality results. Required Candidate profile Strong knowledge of SAS programming language and its applications in clinical trial data analysis. Experience with Veeva or similar systems is desirable.

Analyze and interpret complex clinical trial data to inform business decisions.Develop and maintain databases, spreadsheets, and reports using SAS and Veeva.Collaborate with cross-functional teams Required Candidate profile Strong proficiency in SAS programming language and Veeva software. Experience working with large datasets and performing complex data analysis tasks. Excellent problem-solving skills

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. Required Candidate profile 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

Design, develop, and maintain clinical data systems using R/SQL.Collaborate with cross-functional teams to ensure data quality and integrity.Develop and implement data validation and verification processes. Required Candidate profile Strong knowledge of R/SQL programming languages. Experience working with clinical data systems and databases. Understanding of data modeling and data warehousing concepts.

Analyze and interpret complex clinical trial data to inform business decisions.Develop and maintain databases, spreadsheets, and reports using SAS and Veeva.Collaborate with cross-functional teams to design Required Candidate profile Strong knowledge of SAS programming language and Veeva software. Experience working with large datasets and performing complex data analysis tasks. Excellent problem-solving skills

Analyze and interpret complex clinical trial data to inform business decisions.Develop and maintain databases, spreadsheets, and reports using SAS and Veeva.Collaborate with cross-functional teams Required Candidate profile Strong understanding of clinical trial design, protocols, and statistical analysis plans. Proficiency in programming languages such as SAS and Veeva. Experience with data management systems

Design, develop, and implement Veeva EDC clinical programming solutions for clients.Collaborate with cross-functional teams to ensure seamless integration of EDC systems.Develop and maintain technical documentation Required Candidate profile Strong knowledge of Veeva EDC clinical programming principles and practices. Experience with EDC system implementation and maintenance. Excellent problem-solving skills and attention to detail.

Analyze and interpret complex clinical trial data using SAS. Develop and maintain databases, data systems, and computer models for clinical trial management. Collaborate with cross-functional teams. Required Candidate profile Strong proficiency in SAS programming language. Experience with Veeva or similar clinical trial management systems. Excellent analytical, problem-solving, and communication skills.

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.

Hi , We are hiring for Leading ITES Company for SDTM Programmer Profile. To Apply, WhatsApp 'Hi' @ 9151555419 Follow the Steps Below: >Click on Start option to Apply and fill the details >Select the location as Other ( to get multiple location option ) a) To Apply for above Job Role ( Mumbai ) Type : Job Code # 208 b) To Apply for above Job Role ( Pune ) Type : Job Code # 209 Key Skills : Looking for an SDTM programmer with Min 3 + years experience in SDTM programming and SAS programming Should have good knowledge of CDISC standards, Trial Design domains, Define Qualifications - Health Care Professional OR Masters/Bachelor’s degree in Life Sciences/Physician Please go through the JD and we w...

Participate in the 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 These tasks are to be performed independently or team based with guidance and supervision About The Role Produce and track reports for various line functions within Global Drug Development, used for ongoing monitoring of clinical data Provide understandable and actionable reports on clinical data and monitoring of clinical data for key stakeholders Facilitate interaction with en...