sdtm

Job Title: SDTM Programmer Experience: 6+ Years Industry: Clinical Research / Pharmaceutical / Biotechnology Employment Type: Full-time Job Summary We are looking for an experienced Senior SDTM Programmer with a minimum of 6 years of relevant experience in clinical data programming. The candidate will be responsible for CRF annotation, developing,...

Job Title: SDTM Programmer Experience: 6+ Years Industry: Clinical Research / Pharmaceutical / Biotechnology Employment Type: Full-time Job Summary We are looking for an experienced Senior SDTM Programmer with a minimum of 6 years of relevant experience in clinical data programming. The candidate will be responsible for CRF annotation, developing,...

Job Title: SDTM Programmer Experience: 6+ Years Industry: Clinical Research / Pharmaceutical / Biotechnology Employment Type: Full-time Job Summary We are looking for an experienced Senior SDTM Programmer with a minimum of 6 years of relevant experience in clinical data programming. The candidate will be responsible for CRF annotation, developing,...

Job Title: SDTM Programmer Experience: 6+ Years Industry: Clinical Research / Pharmaceutical / Biotechnology Employment Type: Full-time Job Summary We are looking for an experienced Senior SDTM Programmer with a minimum of 6 years of relevant experience in clinical data programming. The candidate will be responsible for CRF annotation, developing,...

Job Title: SDTM Programmer Experience: 6+ Years Industry: Clinical Research / Pharmaceutical / Biotechnology Employment Type: Full-time Job Summary We are looking for an experienced Senior SDTM Programmer with a minimum of 6 years of relevant experience in clinical data programming. The candidate will be responsible for CRF annotation, developing,...

Job Title: SDTM Programmer Experience: 6+ Years Industry: Clinical Research / Pharmaceutical / Biotechnology Employment Type: Full-time Job Summary We are looking for an experienced Senior SDTM Programmer with a minimum of 6 years of relevant experience in clinical data programming. The candidate will be responsible for CRF annotation, developing,...

Job Title: SDTM Programmer Experience: 6+ Years Industry: Clinical Research / Pharmaceutical / Biotechnology Employment Type: Full-time Job Summary We are looking for an experienced Senior SDTM Programmer with a minimum of 6 years of relevant experience in clinical data programming. The candidate will be responsible for CRF annotation, developing,...

Role Summary We are seeking a highly skilled clinical Data Engineer. You will combine clinical data expertise with strong data engineering and technical skills to generate well documented pipelines from source to curated data sets in common data models like CDISC SDTM. You will collaborate closely with clinical SMEs, data scientists, infrastructure, and...

Role: Senior Developer Location - Chennai / Noida (Only) Job Summary looking for clinical SAS programmers with 3-5 yrs of exp in SDTM domain. should have good SDTM Mapping knowledge, good analytical skills, should have worked on SAS macro's. Good comm skills. Must be reporting to office at least 3 days a week. Key Responsibilities SAS programs, SDTM...

Skill required: Clinical Data Services - Medical Monitoring Designation: Clinical Data Svs Analyst Qualifications:BE,MSc,Bachelor of Pharmacy Years of Experience:3- 5 years About Accenture Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills...

Work Schedule Second Shift (Afternoons) Environmental Conditions Office Job Description Join Us as a Senior Programmer Analyst II – Make an Impact at the Forefront of Innovation The Senior Programmer Analyst II performs advanced statistical and clinical programming activities to support clinical research projects. The role requires strong expertise in...

Skill required: Clinical Data Services - Medical Monitoring Designation: Clinical Data Svs Analyst Qualifications:BE,MSc,Bachelor of Pharmacy Years of Experience:3- 5 years About Accenture Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills across...

Prinicipal Clinical Data Standards ConsultantICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers,...

Sponsor-dedicated: Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Senior Statistical Programmer, you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where...

Prinicipal Clinical Data Standards Consultant ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers,...

Job Overview:Assist in the development and implementation of solutions to global technical service issues and concerns regarding EDC or SAS or other proprietary software, including proactive prevention strategies. Develop/validate Custom/Complex SDTM/SAS datasets/Listings/reports. Efficiently handle external data and data reconciliations. Responsible for...

Sponsor-dedicated: Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Principal Statistical Programmer, you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where...

Overview Work as a programmer on clinical and non-clinical trials; producing non-complex datasets and outputs to excellent quality whilst adhering to deliverable timelines. Awareness of CDISC SDTM and ADaM implementation guidelines; reviewing and updating non-efficacy/non-complex data specifications; creating and debugging simple macros; understanding...

What you will be doing As a Senior Clinical Data Standards Consultant at ICON Plc, you will be responsible for: Developing tools to aid in the implementation and compliance of CDISC, Sponsor, and ICON standards. Collaborating with cross-functional teams to define data collection strategies and standards for clinical trials. Developing and maintaining...

Career Category Research Job Description Amgen is expanding its global Biomedical Data Stewardship (BMDS) capabilities, with Amgen India (AIN) playing a key role in integrated delivery. As Associate Director and Standards Lead, you will lead the India-based BMDS standards team and advance consistent clinical data standards across the development...