Careers

Careers

We provide unparalleled professional services in clinical data analytics and functional outsourcing biometrics in all over the world. A leading innovator, most trusted, and most valuable in Life Sciences vertical, Vita Data teams with clients to develop and deliver full service, scalable data solutions in pharmaceutical, Biotechnology, Medical Device, & CRO industries. Our growth and success is our strong multi-cultural diverse workforce from different nationalities. Our team is our most valuable asset and they have taken Vita Data Science to the heights that it has scaled because of their and is now working to yield it further up on its high growth. We are dedicated to hiring remarkably talented people who are self-directed, determined and smart, often favoring ability over experience and encourage them professionally. Our multi-cultural work environment provides opportunities to enhance their challenging roles with clear responsibilities and the opportunity to work on a variety of assignments.

At VDS, you will have an inspiring trust-based work culture for learning with motivational, approachable and visionary leadership. Working at VDS you will see the impression of an exciting environment to work and grow.

Responsibilities

Develop statistical programs in SAS to generate the clinical datasets, tables, listings and figures.
Perform validation and QC of the programs, datasets and statistical reports per study requirements.
Develop and review CDISC SDTM and ADaM mapping specifications.
Responsible for study closeout and providing submission-ready statistical programming deliverables to the client.
Ensure compliance of CDISC SDTM and ADaM datasets by running OpenCDISC validator and documenting issues.
Generate and review submission documents such as define.xml, SDTM annotated CRF, and reviewers guide.
Ensure review of study documents such as Protocol, CRF, and SAP.
Communicates effectively within a project team to complete assigned tasks on time and within budget.
Effectively implement and promote use of established standards, SOP and best practices.
Provide training and mentoring to junior programmers in the team.

Requirements

Master’s degree or equivalent and relevant formal academic / vocational qualification.
3yrs SAS programming experience.
1yr CDISC implementation experience.
Proficient in SAS and Macros and have developed macros to automate functionality.
Experience working in Oncology therapeutic area
Participated as production or QC programmer at a product and/or study level.
Good organizational, interpersonal, leadership and communication skills.
Ability to independently manage multiple tasks and projects.

To apply, please reach out to info@vitadatasciences.com, with “APPLICATION – SENIOR STATISTICAL PROGRAMMER LEVEL I” as the subject line

Responsibilities

Develop statistical programs in SAS to generate the clinical datasets, tables, listings and figures.
Perform validation and QC of the programs, datasets and statistical reports per study requirements.
Develop and review CDISC SDTM and ADaM mapping specifications.
Responsible for study closeout and providing submission-ready statistical programming deliverables to the client.
Ensure compliance of CDISC SDTM and ADaM datasets by running OpenCDISC validator and documenting issues.
Generate and review submission documents such as define.xml, SDTM annotated CRF, and reviewers guide.
Ensure review of study documents such as Protocol, CRF, and SAP.
Communicates effectively within a project team to complete assigned tasks on time and within budget.
Effectively implement and promote use of established standards, SOP and best practices.
Provide training and mentoring to junior programmers in the team.

Requirements

Master’s degree or equivalent and relevant formal academic / vocational qualification.
5yrs SAS programming experience.
1-2yrs CDISC implementation experience.
Proficient in SAS and Macros and have developed macros to automate functionality.
Participated as production or QC programmer at a product and/or study level.
Experience working in Oncology, CNS or Rare Disease therapeutic areas.
Good organizational, interpersonal, leadership and communication skills.
Ability to independently manage multiple tasks and projects.

To apply, please reach out to info@vitadatasciences.com, with “APPLICATION – SENIOR STATISTICAL PROGRAMMER LEVEL II” as the subject line

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