Work as Clinical Data Svs Associate at 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 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries.

Post : Clinical Data Svs Associate

Job Description
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.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.A critical phase in clinical research that assures collection, integration and availability of data at appropriate quality and cost. It also supports the conduct, management and analysis of studies across the spectrum of clinical research as defined by the National Institutes of Health (NIH)

Candidate Profile : Overall 2-5 years of experience with exposure to Medidata RAVE EDC platform preferred.
• Comprehensive data management expertise - deliver efficient, quality data management products focused on meeting customer needs.
• Strong understanding of clinical trial processes, data management principles and regulatory guidelines.
• Attention to detail and accuracy in work.
• Excellent organizational, communication, and data management skills (detail oriented).

Additional Information
Experience : 2-5 years
Qualification : Any Graduation
Location : Bengaluru
Industry Type : Pharma/ Healthcare/ Clinical research
Skill required : Clinical Data Services
End Date : 20th August 2026