Clinical Data Svs Associate

 About The Role  

Skill required: Clinical Data Services - SAS Clinical

Designation: Clinical Data Svs Associate

Qualifications:BE/MSc/Bachelor of Pharmacy

Years of Experience:1 to 3 years
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. 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 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.Data Integration tool which organizes, standardizes and manages clinical research data and metadata. It provides the foundation to define analysis data sets and support strategic analyses such as cross study and advanced safety analysis.

What are we looking for?

Adaptable and flexible

Ability to work well in a team

Written and verbal communication

Roles and Responsibilities: Review approved Protocol and Study Setup documentsDevelop SAS programs/run standard macros for generating SDTM Like Datasets, SDTM Datasets Tables, Listings, Figures and Trial Specific OutputsPerform and document developer testingResponsible for validation of the SDTM Like Datasets, SDTM datasetsTables Listings Figures and Trial Specific OutputsExtract data from available databases and place data into SAS or other types of data files.Create and review Submissions Documents, Specifications for safety/standard outputs.Adhere to all client and Accenture SOPs as applicableEnhance technical skills relevant to statistics and programmingComplete all required and adequate trainings
 Qualification BE,MSc,Bachelor of Pharmacy