Eurofins: Data Configuration Specialist — Bengaluru, KA, India

Eurofins lists a Data Configuration Specialist opening in Bengaluru, KA, India. The position is listed as full-time. The job description covers clinical trials, laboratory testing, project management, key-account planning.

Recruitment overview

OrganisationEurofins
Post / roleData Configuration Specialist
DepartmentTesting & Laboratory
Employment typeFull-time
Notification / job IDREF35062I
Job locationBengaluru, KA, India
Work arrangementOn-site
Educational qualificationDegree / qualification: Bachelor degree in a related field
Experience requiredMinimum 2 years work experience
Salary / stipendSee employer notice for pay details
Last date to applySee official notice

About Eurofins

Eurofins provides analytical testing and laboratory services across life sciences and other industries. Its work includes assessing food, water, pharmaceutical and cosmetic products for qualities such as safety, authenticity, composition and accurate labelling. The employer also describes activities in genomics, clinical-study support, biopharmaceutical development and manufacturing, and diagnostic testing. Scientific methods and dependable information are central to this business, supported by the technology and operational functions used to deliver laboratory services.

The position and its setting

Eurofins lists Data Configuration Specialist in Bengaluru, KA, India, under reference REF35062I. The details below separate the work described by the employer from essential conditions, preferred experience and practical preparation advice.

  • Department: Testing & Laboratory
  • Employment type: Full-time
  • Employer listing date: 18 July 2022
  • Legal Entity: Others
  • Contract Type: Permanent
  • Business Lines: Other Business Line
  • Brands: Eurofins India Biopharma Services

Responsibilities and work described

  • Purpose of the Job and Expected outcome
  • Configure the Laboratory Information Management System LIMS dbase throughout the duration of the study inline with the Clinical Protocol, performing appropriate QC controls according to global procedures and agreed specifications
  • Quality / delivery: that the electronic data generated is transferred to the customer as per the Data Specifications
  • Key Accountabilities Data Configuration Specialist supports activities for studies during all stages in such a way that:
  • Tasks have been carried out independently, and the status or result is communicated back to all relevant parties
  • Database to be set up as per client protocol
  • Configure the study-specific requirements in the (LIMS) for central laboratory testing in clinical trials
  • (e.g. visit schedule, testing panels and flagging)
  • Collaboration: with project management, laboratory, IT and clients
  • Is aware of key study milestones and prioritizes study activities to achieve the timelines
  • Format the Database as per desired type of data
  • Quality / delivery: that LIMS and other systems are correctly configured in line with study Priming Document
  • Maintenance: complete and current version controlled Data Study Files

Essential requirements and candidate background

  • Minimum 2 years work experience
  • Education:
  • Bachelor degree in a related field

Location, schedule and contract conditions

  • Work arrangement: On-site
  • Advertised location: Bengaluru, KA, India

Pay and application dates

A verified salary figure is not established in this article. An online estimate for another Data Configuration Specialist vacancy is not an offer for reference REF35062I; use the employer’s own pay disclosure and recruitment communication.

A closing date is not confirmed in this article. Check the current employer page before submitting: an undated posting can change or be withdrawn.

How to apply to Eurofins

Applications follow the official employer page linked below.

Open the official Eurofins posting below and match the title and reference REF35062I.

Compare your qualifications and experience with the essential conditions for the Bengaluru, KA, India position, then read the preferred criteria separately.

Prepare an accurate CV and the supporting items requested in that employer’s application. Provide only information and documents you are authorised to share.

Use the employer’s application option, complete the required fields and review the submission. Retain the acknowledgement when one is provided. Job Alerts World does not receive the application.

Practical preparation: clinical trials

For clinical-trial work, describe the study function and responsibilities you were authorised to perform. Useful context can include coordination, documentation, data or site work, depending on the post.

Relevant skills

  • clinical trials
  • laboratory testing
  • project management
  • key-account planning

Important links

Official notification / job descriptionOpen official page
Online application portalOpen official page

Read the complete official notice before applying. Availability and requirements can change.

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