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Accenture | Hiring | Sr. Clinical Data Management Associate | Bengaluru | BigDataKB.com | 6 Oct 2022

Job Location: Bengaluru

Skill required: Clinical – Clinical EDC Design

Designation: Sr. Clinical Data Management Associate

Job Location: Bengaluru

Qualifications: BSc/MSc/P G Diploma In Clinical Research

Years of Experience: 3-5 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?

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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 design Electronic Case Report Form specifications in the EDC environment, Data Validation Specification, and time & events by reviewing the protocol concept sheet.

What are we looking for?


We are looking for individuals who have the following skillset:

  • Ability to establish strong client relationship
  • Ability to handle disputes
  • Ability to manage multiple stakeholders
  • Ability to meet deadlines

It would be a value add if you are proficient in:

  • Clinical Trial Setup Admin
  • Clinical Trial Site & Investigator Mgmt

Roles and Responsibilities

  • In this role, you are required to analyze and solve lower-complexity problems
  • Your day to day interaction is with peers within Accenture before updating supervisors
  • You may have limited exposure with clients and/or Accenture management
  • You will be given moderate level instructions on daily work tasks and detailed instructions on new assignments
  • 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 expected to constantly be on the lookout for ways to enhance value for your respective stakeholders/clients
  • The decisions you make impact your 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 this role may require you to work in rotational shifts.

BSc/MSc/P G Diploma In Clinical Research




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