Clinical Data Svs Specialist

Skill required: Clinical Data Operations - SAS Clinical
Designation: Clinical Data Svs Specialist
Qualifications:MSc/Bachelor of Pharmacy/P G Diploma In Clinical Research
Years of Experience:7 to 11 years
Language - Ability:English(Domestic) - Expert
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 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. we majorly works on statistical programming for ADAM and TFLS Clinical Data Operations involves the management and oversight of data collected during clinical trials. This includes data collection, validation, storage, and analysis to ensure accuracy and compliance with regulatory standards. 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. 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? we are looking for candidate with 7 to 11 years of experience . proficient in ADAM and TLF we are looking for candidate with 7 to 11 years of experience . proficient in ADAM and TLF
Certifications: SAS Certified Base Programmer for SAS 9 - SAS; SAS Certified Clinical Trials Programmer Using SAS 9 - SAS
Roles and Responsibilities: •In this role you are required to do analysis and solving of moderately complex problems • May create new solutions, leveraging and, where needed, adapting existing methods and procedures • The person would require understanding of the strategic direction set by senior management as it relates to team goals • Primary upward interaction is with direct supervisor • May interact with peers and/or management levels at a client and/or within Accenture • Guidance would be provided when determining methods and procedures on new assignments • Decisions made by you will often impact the team in which they reside • Individual would manage small teams and/or work efforts (if in an individual contributor role) at a client or within Accenture • Please note that this role may require you to work in rotational shifts

MSc,Bachelor of Pharmacy,P G Diploma In Clinical Research