Senior Clinical Data Specialist

IQVIA

Ernakulam

On-site

INR 700,000 - 900,000

Full time

14 days+
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Job summary

IQVIA is seeking a Clinical Data Specalist / Senior Clinical Data Coordinator in India to provide data management expertise within the CDM team and may undertake leadership activities under supervision. The role involves supporting data operations, data reviews, clarifications, and potentially leading database audits and testing.

Candidate should have a clinical/biological/scientific degree and strong attention to detail, with ability to work independently and communicate effectively with

Qualifications

  • Medical terminology exposure.
  • Excellent organizational, communication, leadership and computer skills.
  • Ability to exercise excellent attention to detail. Ability to act independently and with initiative required to resolving problems.

Responsibilities

  • Serve as a Data Operations Coordinator (DOC) for one protocol with less then 5 operations staff (excludes DE) or 15+ easy to moderately complex central laboratory studies, or lead a data management task with guidance.
  • May serve as back-up to a DOC or DTL.
  • May conduct data review.
  • May write and resolve data clarifications.
  • May lead database audit team.
  • May develop and test databases and edit specifications.
  • May perform testing of programming.
  • May perform clinical data coding.

Skills

Medical terminology exposure
Leadership
Communication
Attention to detail

Education

Bachelor's Degree in Clinical, biological or mathematical sciences or related field

Job description

Clinical Data Specalist / Senior clinical Data Coordinator
Job Overview

Provide basic and some comprehensive data management expertise to the Clinical Data Management (CDM) team to provide efficient, quality data management products that meet customer needs. May also undertake team leadership activities under the supervision of the Data Operations Coordinator (DOC), Data Team Lead (DTL), or Functional Manager.

Essential Functions
  • Serve as a Data Operations Coordinator (DOC) for one protocol with less then 5 operations staff (excludes DE) or 15+ easy to moderately complex central laboratory studies, or serve in a leadership role in a specific data management task (e.g., coder, tester or database designer for technologies that don't require extensive programming expertise) with guidance.
  • May serve in the role of back-up to a DOC or DTL.
  • May conduct data review.
  • May write and resolve data clarifications.
  • May lead database audit team.
  • May develop and test databases and edit specifications.
  • May perform testing of programming.
  • May perform clinical data coding.
Qualifications
  • Bachelor's Degree Clinical, biological or mathematical sciences, or related field Req
  • Equivalent combination of education, training and experience in lieu of degree.
  • Medical terminology exposure. Excellent organizational, communication, leadership and computer skills. Ability to exercise excellent attention to detail. Ability to act independently and with initiative required to resolving problems. Ability to establish and maintain effective working relationships with coworkers, managers and clients. Medical terminology exposure. Excellent organizational, communication, leadership and computer skills. Ability to exercise excellent attention to detail. Ability to act independently and with initiative required to resolving problems. Ability to establish and maintain effective working relationships with coworkers, managers and clients.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Experience Level

Senior Level

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