Clinical Data Svs Associate

Full-Time @Accenture in IT
  • Post Date : July 3, 2024
  • Apply Before : September 30, 2024
  • 0 Application(s)
  • View(s) 59
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Job Detail

  • Job ID 10638

Job Description

Job description


Skill required:
 Clinical Data Operations – Clinical Database Testing

Designation:
 Clinical Data Svs Associate

Qualifications:
BE/MSc

Years of Experience:
1 to 3 years

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.The Clinical Data Management team focuses on the collection, integration, and availability of data at appropriate quality and cost. The team is responsible for performing data management activities including discrepancy review, query generation, and resolution. The team is also responsible for creating CRF Completion Guidelines (CCG) and SAE reconciliation guidelines. 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.You will be expected to design and test EDC databases, create and maintain User Acceptance Testing (UAT) procedures for EDC systems, including the creation of test plans, verification of requirements for databases, eCRFs, edit checks, extractions, and reports.

What are we looking for?

  • Clinical Database Testing
  • Performance Testing Strategy
  • Automated Testing
  • Ability to manage multiple stakeholders
  • Ability to perform under pressure
  • Agility for quick learning 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 own team and direct supervisor
  • You will be provided detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments
  • The decisions that you make would impact your own work
  • You will be an individual contributor as a part of a team, with a predetermined, focused scope of work
  • Please note that this role may require you to work in rotational shiftsQualificationBE,MSc

Role: Clinical research Scientist
Industry Type: IT Services & Consulting
Department: Research & Development
Employment Type: Full Time, Permanent
Role Category: Pharmaceutical & Biotechnology
Education
UG: Any Graduate
PG: Any Postgraduate

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