Current jobs related to Sdtm Programmer - Bengaluru Karnataka - Novo Nordisk

  • Statistical Programmer 1

    4 months ago

    Bengaluru, Karnataka, India Fortrea Full time

    As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

  • Principal Statistical Programmer

    4 months ago

    Bengaluru, Karnataka, India Fortrea Full time

    As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

  • Principal Stats Programmer

    3 months ago

    Bengaluru, Karnataka, India Fortrea Full time

    As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

  • Principal Statistical Programmer

    4 months ago

    Bengaluru, Karnataka, India Fortrea Full time

    As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

  • Statistical Programmer 2

    3 months ago

    Bengaluru, Karnataka, India Fortrea Full time

    As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

  • Principal Statistical Programmer

    4 months ago

    Bengaluru, India Fortrea - Organic Full time

    As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

  • Principal Stats Programmer

    4 months ago

    Bengaluru, India Fortrea - Organic Full time

    As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

  • Principal Statistical Programmer

    5 months ago

    Bengaluru, India Novotech Asia Full time

    **Brief Position Description**: The Principal Statistical Programmer (PSP) is primarily responsible for all statistical programming aspects, and/or acts as Lead Programmer, across several studies. The PSP will act as the Statistical Programming Coordinator and may provide ongoing supervision of an assigned portfolio of projects to ensure timely and...

  • Clinical SAS Programmer

    3 months ago

    Bengaluru, India Element Technologies Inc Full time

    We are looking for Clinical SAS programmers with the following skills: 1. Should have relevant experience in SDTM, ADAM & TLF. 2. Should know to write specifications. 3. Should write programs from scratch 4. Should be in CRT file creation. 5. Can u do a pinnacle report. 6. Should have created data sets. 7. Should have knowledge on XML. 8. Should know...

  • Principal Statistical Programmer

    5 months ago

    Bengaluru, India PHASTAR Full time

    Overview: Work as a principal programmer across multiple clinical and non-clinical studies; supporting regulatory submission activities; producing and validating datasets and outputs to excellent quality whilst adhering to deliverable timelines. Excellent knowledge of CDISC SDTM and ADaM implementation guidelines working independently in this area;...

  • Statistical Programmer

    4 months ago

    Bengaluru, Karnataka, India Clario Full time

    Are you seeking a purposeful and rewarding SAS programming career opportunity? - Our statistical programming team is growing in India, and with big ambitions and a clear vision for the future, now is the time to join Clario! - What we offer: - Competitive compensation- - Attractive benefits (security, flexibility, support and well-being)- - Engaging employee...

  • Senior Statistical Programmer

    2 weeks ago

    Bengaluru, India Cytel Full time

    Job Title: Senior Statistical ProgrammerLocation: India (Remote) / Hybrid (Open to Pune / Hyderabad)We are experiencing exponential growth on a global scale and hiring Senior Statistical Programmers to join our FSP division. You will apply your know-how in CDISC standards (SDTM & ADaM) and advanced SAS programming skills, to support or lead one or more...

  • Senior Statistical Programmer

    4 months ago

    Bengaluru, India IQVIA Full time

    Job Profile: Senior Statistical Programmer Functional Area Statistical Programming Education Requirements: • Bachelor's degree from reputable university preferably in science/ mathematics related fields • Attained SAS® certification Technical Skills Requirements • Must have excellent knowledge of SAS® Base, and good knowledge of SAS® graph and...

  • Principal Statistical Programmer

    3 months ago

    Bengaluru, Karnataka, India ClinChoice Full time

    ClinChoice is a global full-service CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative "one-team" culture. We are looking for a dynamic person to join our in-house team as a Principal Statistical Programmer on a permanent basis. You will work on projects from our varied client base,...

  • Clinical SAS Programmer

    2 weeks ago

    Bengaluru, Karnataka, India Clini launch Business Solutions Full time

    Job Summary We are seeking a skilled and detail-oriented Clinical SAS Programmer to join our team. The Clinical SAS Programmer will be responsible for developing, validating, and maintaining SAS programs for analyzing clinical trial data. The role involves working closely with biostatisticians, clinical researchers, and data management teams to ensure...

  • SAS Programmer

    2 months ago

    Bengaluru, India Clario Full time

    Are you seeking a purposeful and rewardingSAS programmingcareer opportunity?Our eCOA team is growing in India, and with big ambitions and a clear vision for the future, now is the time to join Clario as a Systems Analyst II.What we offerCompetitive compensation + shift allowancesAttractive benefits (security, flexibility, support and well-being)Engaging...

  • Statistical Programmer Ii

    4 months ago

    Bengaluru, India Ergomed Full time

    Company Description Ergomed PLC is a rapidly expanding full service mid-sized CRO specialising in Oncology and Rare Disease. Since its foundation in 1997 the company has grown organically and steadily by making strategic investments and landmark acquisitions, with operations in Europe, North America and Asia Our company allows for employee visibility (you...

  • Sas Programmer

    7 days ago

    Bengaluru, Karnataka, India Emmes Full time

    Overview: Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into...

  • Senior Statistical Programmer

    1 month ago

    Bengaluru, India eClinical Solutions Full time

    KEY TASKS & RESPONSIBILITIES • Develop specifications for SDTM datasets and SDTM datasets specifications for Clinical Data Analysis.• Develop SAS programming to produce SDTM datasets and SDTM datasets. • Develop specifications for Analysis Data Model (ADaM) datasets. • Develop SAS programming and validation of ADaM datasets for trial level reporting...

  • Senior Statistical Programmer

    1 month ago

    Bengaluru, India eClinical Solutions Full time

    KEY TASKS & RESPONSIBILITIES • Develop specifications for SDTM datasets and SDTM datasets specifications for Clinical Data Analysis.• Develop SAS programming to produce SDTM datasets and SDTM datasets. • Develop specifications for Analysis Data Model (ADaM) datasets. • Develop SAS programming and validation of ADaM datasets for trial level reporting...

Sdtm Programmer

3 months ago

Bengaluru Karnataka, India Novo Nordisk Full time

SDTM Programmer

**Category**:Data & AI**Location**:Bangalore, Karnataka, IN**Department: SDTM Programming & Submission**About the department**

Bangalore Global Development, Global Business Service (GBS), SDTM Programming & Submission team was established in April 2016 and became a separate department in July 2021. The team has a good blend of experience and fresh perspective and comprises experienced SDTM Subject Matter and Submission experts, who form the core of the team. The main purpose & objective is to ensure high quality compliant submission ready SDTM packages in close collaboration with our stakeholders across the clinical landscape, for all clinical trials within Novo Nordisk.**The Position**
- A SDTM Programmer will be responsible for ensuring compliance with Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), Good Documentation Practice (GDP), and Good Programming Practice (GPP) and promote the exchange of knowledge within the organization and externally via participation in meetings/conferences. The Senior SDTM Programmer is recognized as responsible for supporting end users and must act independently, following the strategic objectives of the standards governance bodies and the company in general. The Senior SDTM Programmer will be responsible for assisting in solving methodological or technical demanding tasks where innovation is a key element.- Responsible for finalizing Study Data Tabulation Model (SDTM) deliverables and to review of eCRFs, special attention should be given to non-standard modules, regarding the impact on SDTM.
- Perform custom programming as required and validate according to relevant SOP.
- Run Pinnacle 21 checks and resolve issues by coordinating with the Trial squad. Ensure compliance to the Novo Nordisk SDTM Implementation Guide (NN SDTMIG).
- Responsible for reviewing and providing inputs to data collection requirements in relation but not limited to Protocol, Flow chart, electronic CRFs (eCRF), External Specifications, SDTM Domains.
- Prepare & review metadata specification (as relevant) and aCRF. Submit requests to Standards Teams to either deviate from an existing standard or use a trial-specific element in alignment with Lead SDTM Programmer.

**Qualifications**- Bachelor's or Masters in life sciences, natural sciences, pharmacy, veterinary science, engineering, clinical information management, computer science or equivalent qualifications.
- Minimum 2 -5 years of experience in the Life Sciences industry and preferably 4 years within Clinical Data Management and with hands-on experience in Clinical Data Interchange Standards Consortium (CDISC) SDTM.
- Excellent communication skills
- Expert knowledge of end-to-end clinical data management activities.
- Experience with collaboration across regional borders.
- Experience with mentoring and presentations.
- Participation in conferences/workshops.
- Demonstrated experience with project management.
- Ability to work in a diverse multi-cultural environment.
- Good knowledge of GxP and other guidelines within drug development.

**Working at Novo Nordisk**
- Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around the world and impacting more than 40 million patient lives daily. All of this has made us one of the 20 most valuable companies in the world by market cap. Our success relies on the joint potential and collaboration of our more than 63,000 employees around the world. We recognize the importance of the unique skills and perspectives our people bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk, we're working toward something bigger than ourselves, and it's a collective effort. Join us Together, we go further. Together, we're life changing.**Contact**-
**Deadline**
- 17th April 2024- We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.- At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.