Clinical Data Programming Associate

  Pharmacovigilance

Job title: Clinical Data Programming Associate

Company: Accenture

Job description: Skill required: Clinical – Clinical Database Programming Designation: Clinical Data Programming Associate About Accenture Accenture is a global professional services company with leading capabilities in digital, cloud and security. Combining unmatch

Skill required: Clinical – Clinical Database Programming Designation: Clinical Data Programming Associate 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 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. You will be working as a part of the Study Startup team which is responsible for Project Initiation, Planning, Implementation, Control & Evaluation and Close-Out activities which includes initiation of trial capacity, trial setup activities, etc. You will be expected to develop and review complex edit checks, patient profile listings, reports, preprocessing checks & map datasets for validation based on study requirements using different tools/techs such as Cognos / SAS, J-Review, or any other applicable systems. What are we looking for We are looking for individuals who have the following skillset: Clinical Data Management Clinical EDC Build Adaptable and flexible Ability to perform under pressure Ability to work well in a team Ability to manage multiple stakeholders Ability to meet deadlines Roles and Responsibilities In this role, you are required to solve routine problems, largely through precedent and referral to general guidelines Your expected interactions are within your team and direct supervisor You will be provided detailed to a moderate level of instruction on daily work tasks and detailed instruction on new assignments and the decisions that you make that would impact your work You will need to be well versed with basic statistics and terms involved in the day to day business and use it while discussing with stakeholders You will be required to help in the overall team’s workload by managing your deliverables and help the team when required You will be an individual contributor as a part of a team, with a predetermined focused scope of work. Please note this role may require you to work in rotational shifts.

Expected salary:

Location: Bangalore, Karnataka

Job date: Thu, 14 Jul 2022 22:47:26 GMT

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