Clinical Data Svs Analyst

Skill required: Clinical Data Operations - Clinical Data Management

Designation: Clinical Data Svs Analyst

**Qualifications:**MSc/Bachelor Degree in Life Sciences/Master Degree in Life Sciences

**Years of Experience:**2 to 5 years

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 world 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 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.
A critical phase in clinical research that assures collection, integration and availability of data at appropriate quality and cost. It also supports the conduct, management and analysis of studies across the spectrum of clinical research as defined by the National Institutes of Health (NIH).

What are we looking for Proficiency in Medical Coding
Experience in Data management activities

Roles and Responsibilities:- In this role you are required to do analysis and solving of lower-complexity problems

• Your day to day interaction is with peers within Accenture before updating supervisors

• In this role you may have limited exposure with clients and/or Accenture management

• You will be given moderate level instruction on daily work tasks and detailed instructions on new assignments

• The decisions you make impact your own work and may impact the work of others

• You will be an individual contributor as a part of a team, with a focused scope of work

• Please note that this role may require you to work in rotational shifts

• Perform medication coding of medications and adverse events using relevant coding dictionaries.

• Any other data management activities as assigned or necessary

  Qualification MSc,Bachelor Degree in Life Sciences,Master Degree in Life Sciences