Clinical Data Svs Sr Analyst

Skill required: Clinical Data Services - Medical Monitoring
Designation: Clinical Data Svs Sr Analyst
Qualifications:BE/MSc/Bachelor of Pharmacy
Years of Experience:4 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 world s leading biopharma companies bring their vision to life s 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? •Written and verbal communication •Ability to work well in a team •Agility for quick learning •Problem-solving skills
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 •Review approved Protocol and Study Setup documents Develop SAS programs/run standard macros for generating SDTM Like Datasets, SDTM Datasets Tables, Listings, Figures and Trial Specific Outputs Perform and document developer testing Responsible for validation of the SDTM Like Datasets, SDTM datasets, Tables Listings Figures and Trial Specific Outputs Extract 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 applicable Enhance technical skills relevant to statistics and programming Complete all required and adequate trainings Mentor new hires associates in their new roles, assist with questions, and provide guidance for successful delivery. To carry out other responsibilities as and when assigned by the India Service Delivery Lead/Statistical Programmer Manager/Senior Statistical Programmer.