Skill required: Clinical Data Services - SAS Clinical

Designation: Clinical Data Svs Sr Analyst

Qualifications:BE

Years of Experience:5 to 8 years

Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Songall powered by the worlds largest network of Advanced Technology and
What would you do You will be aligned with our Life Sciences RD 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 worlds 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 Ability to establish strong client relationship
Ability to handle disputes
Ability to manage multiple stakeholders
Ability to meet deadlines
Ability to perform under pressure

Roles and Responsibilities: Overall experience of 4+ years in Clinical review and reporting programming,
business analytics and/or clinical trial setup, gained in the pharmaceutical
industry, CRO or Life Science related industry preferred.
o Participate in the lifecycle of producing key data and/or reports in support of
data review reporting development including evaluation of requirements, design
specifications, interface to programmers, report programming, coordinate
validation and rollout activities along with providing quantitative
analytical support.
o Provide understandable and actionable reports on clinical data and monitoring
of clinical data for key stakeholders.
o Facilitate interaction with end user on creating specifications and working with
programmers or performing the programming activities for successful delivery.
o Program reports of various complexity from documented requirements, within
the clinical reporting systems using SQL, PL/SQL, SAS, and JReview etc.
preferred.
o Valuable analytical and communication skills.

Qualification BE

📌 Clinical Data Svs Sr Analyst (Bengaluru)
🏢 Accenture
📍 Bengaluru