Sas programmer Jobs

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Accenture —Bengaluru, Karnataka
- Full-time
- Master's degree
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- Bachelor's degree
Clinical Data Svs Associate Manager
Accenture —Bengaluru, Karnataka
- Full-time
- Master's degree
- Bachelor's degree
- Communication skills
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Triumphant ITCS —India
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Clinical Data Svs Associate Manager
Accenture —Bengaluru, Karnataka
Roles and Responsibilities: •In this role you are required to do analysis and solving of moderately complex problems • Typically creates new solutions,…
Clinical Data Svs Associate Manager
Accenture —Bengaluru, Karnataka
Roles and Responsibilities: •In this role you are required to do analysis and solving of moderately complex problems • Typically creates new solutions,…
12d

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Clinical Data Svs Sr Analyst

Accenture -
Bengaluru, Karnataka

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Job details

Full-time

Qualifications

B.Pharma
Master's degree
Analysis skills
Bachelor's degree
M.Pharma
Macros
Pharmacy
B.E.
Communication skills

Full job description

Skill required: Clinical Data Services - Medical Monitoring
Designation: Clinical Data Svs Sr Analyst
Qualifications:BE/Bachelor of Pharmacy/Master of Pharmacy
Years of Experience:5 to 8 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 more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song— all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. Our 784,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We embrace the power of change to create value and shared success for our clients, people, shareholders, partners and communities.Visit us at www.accenture.com
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 worldâ€™s leading biopharma companies bring their vision to life â€“ enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience. Clinical Data Services involve the management and processing of data collected during clinical trials. This includes data collection, validation, storage, and analysis to ensure the data is accurate and reliable. The goal is to support clinical research by providing high-quality data that can be used to evaluate the safety and efficacy of medical treatments. These services are essential for regulatory compliance and successful trial outcomes. They often utilize specialized software and systems to manage the data efficiently. Provides medical expertise for trial oversight and safety concerns. This includes creation, review and validation of protocol requirement specifications as per the applicable SOP.
What are we looking for? •Strong analytical skills •Written and verbal communication •Problem-solving skills
Roles and Responsibilities: 1. Analyze and solve increasingly complex problems with minimal supervision on routine tasks and moderate guidance on new assignments 2. Interact primarily with Accenture peers, with occasional engagement with clients and Accenture leadership 3. Make decisions impacting own deliverables and potentially the work of others 4. Function as an individual contributor and/or oversee a small workstream or team 5. Work in rotational shifts, if required 6. Act as the interface between study teams, offshore teams, and onshore/client stakeholders 7. Perform Quality Control (QC) checks for standard and non-standard safety and efficacy deliverables 8. Collaborate with Senior Statistical Programmers, study leads, and programmers to ensure smooth study execution 9. Review approved protocols, study setup documents, and submission specifications 10. Develop SAS programs and execute standard macros to generate SDTM-like datasets, SDTM datasets, Tables, Listings, Figures, and trial-specific outputs 11. Perform developer testing and validate datasets and outputs in compliance with standards 12. Maintain project, validation, and programming documentation as per SOP requirements 13. Adhere to all client and Accenture SOPs 14. Mentor and guide new hires; assist with queries and ensure successful onboarding 15. Conduct and evaluate Service Readiness Assessments for new resources 16. Support resource management for ongoing and upcoming studies 17. Assist Statistical Programming Managers / Service Delivery Leads with operational reporting and daily activities 18. Leverage standards to improve efficiency and consistency across projects 19. Complete assigned trainings within defined timelines and continuously enhance technical skills 20. Support non-clinical and organizational initiatives, task forces, and Business Excellence activities

BE,Bachelor of Pharmacy,Master of Pharmacy

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