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Clinical Data Programming Scientist

5.00 to 8.00 Years   Bangalore   05 May, 2022
Accenture
Job LocationBangalore
EducationNot Mentioned
SalaryNot Disclosed
IndustryIT - Software
Functional AreaGeneral / Other Software
EmploymentTypeFull-time

Job Description

    Skill required: Clinical - Clinical EDC Design Designation: Clinical Data Programming Scientist Job Location: Bengaluru Qualifications: BSc/MSc/P G Diploma In Clinical Research Years of Experience: 5-8 years About Accenture Operations 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, Interactive, Technology and Operations services all powered by the world s largest network of Advanced Technology and Intelligent Operations centers. Our 674,000 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.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 and Investigator Management
    Roles and Responsibilities
      • In this role, you need to analyze and solve increasingly complex problems
      • Your day to day interactions is with peers within Accenture
      • You are likely to have some interaction with clients and/or Accenture management
      • You will be given minimal instruction on daily work/tasks and a moderate level of instructions on new assignments
      • You will need to consistently seek and provide meaningful and actionable feedback in all interactions
      • You will be expected to be constantly on the lookout for ways to enhance value for your respective stakeholders/clients
      • Decisions that are made by you will impact your work and may impact the work of others
      • You would be an individual contributor and/or oversee a small work effort and/or team.
    Please note this role may require you to work in rotational shifts.,

Keyskills :
life sciencesclinical trialsdata validationsite initiationbusiness processproject initiationprofessional servicesresearchbusinessstrategy

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