Sdtm Jobs – Apply to Latest Sdtm Job Vacancies

5 - 10 years

1 - 6 Lacs

Bengaluru

Remote

Kindly share your updated resume to heena.gill@qvia.com Role & responsibilities Minimum 6+ Years of experience . Works collaboratively with clinical bioinformatics, biomarker scientists and study statistical programming team, to meet biomarker analysis deliverables and timelines Has knowledge of clinical trial study design and biomarker assay types, including but not limited to Immunohistochemistry, cell phenotype, next gene sequencing. Demonstrate knowledge of CDISC standards for SDTM, ADaM and submission experience to regulatory agencies. Demonstrates SAS programming proficiency, including in depth understanding of graphical template languages and using internal macros or writes SAS macros to automate study deliverables. Demonstrates R programming proficiency in using data science library packages including but not limited to tidyverse, pharmaverse and shiny. Demonstrate statistical knowledge, interpret complex dataset and modeling methods in both SAS and R languages. Must be familiar with Microsoft Excel, Microsoft Word, Adobe PDF. Role & responsibilities

Posted 3 months ago

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Business Advisory Senior Analyst Accenture

5 - 8 years

7 - 10 Lacs

Bengaluru

Work from Office

Skill required: Life Sciences (AR&D) Services - SDTM Programming Designation: Business Advisory Senior Analyst Qualifications: BTech Years of Experience: 5 to 8 years What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the world's leading biopharma companies bring their vision to life - enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.In this role, you will be expected to program mapping of eCRF and external data into SDTM standards using SAS/ETL tools as applicable. What are we looking for? SAS Analytics SAS Clinical SAS Visual Text Analytics Agility for quick learning Adaptable and flexible Ability to work well in a team Ability to perform under pressure Ability to meet deadlines SDTM MappingSAS Roles and Responsibilities: In this role you are required to do analysis and solving of increasingly complex problems Your day to day interactions are with peers within Accenture You are likely to have some interaction with clients and/or Accenture management You will be given minimal instruction on daily work/tasks and a moderate level of instruction on new assignments Decisions that are made by you impact your own work and may impact the work of others In this role you would be an individual contributor and/or oversee a small work effort and/or team Please note that this role may require you to work in rotational shifts Qualifications BTech

Posted 3 months ago

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Study Data Manager: Life Science: Max 20 LPA: Apply Now Outpace Consulting Services

2 - 7 years

10 - 20 Lacs

Pune, Bengaluru, Mumbai (All Areas)

Work from Office

Hi, We are looking to hire someone for Study Data Manager Please go through the JD, we shall call back the relevant Profiles a) Experience in leading clinical studies. b) Experience on Study Conduct and Close Out JOB DECSRIPTION: Need exposure to Inform or Medidata Rave database • Responsible & Accountable for the assigned study conduct activities, in clinical trials • Validate clinical trial data to ensure consistency, integrity, and accuracy based on project-specific guidelines. • Generate data queries based on validation checks or raise Manual queries to resolve data inconsistencies. • To perform reconciliation of data from external sources (e.g. Serious Adverse Events, IWRS, Central Laboratory). • SPOC for the study communications • Proactively highlight any risks associated with the study along with the mitigation plan. • Establish a partnership with the stakeholders at the operational level to work seamlessly to deliver the assigned project/activity as per timelines. • Identify process Improvement opportunities and ensure learning is shared • Ensure deliverables and/or agreed activities/tasks with customers. are completed with the expected quality. • Have worked on Study set-up, Study Conduct, and Study Closeout for various therapeutic areas. • Have also worked on writing edit check specifications, CRF completion guidelines, and review and corrections of set-up documents for different versions To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below: a) For Position in Mumbai Search : Study Data Manager Mumbai (Job Code # 184) b) For Position in Pune Search : Study Data Manager Pune (Job Code # 185) C) For Position in Bangalore Search : Study Data Manager Bangalore (Job Code # 186)

Posted 3 months ago

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