Job Description

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

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. CDISC SDTM Knowledge. SAS programming skills. Clinical Domain Knowledge (Trial Designs). Represent Accenture Services at all times in client interactions by maintaining professional demeanor and conduct consistent with Accenture Values and Code of Ethics. They help identify and raise protocol deviations in the database, perform edit check validation by creating test cases, write test scripts, and carry out database validation (UAT) against the specified CRF/ECRF. The team also managing clinical data management projects. 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?

oAbility to work well in a team oAdaptable and flexible oCommitment to quality oWritten and verbal communication

Roles and Responsibilities:

oIn this role you are required to solve routine problems, largely through precedent and referral to general guidelines o Your expected interactions are within your own team and direct supervisor o You will be provided detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments o The decisions that you make would impact your own work o You will be an individual contributor as a part of a team, with a predetermined, focused scope of work o Please note that this role may require you to work in rotational shifts




BE,MSc,Bachelor of Pharmacy