Clinical Data Specalist / Senior clinical Data Coordinator

IQVIA; Ernakulam; On-site; INR 800,000 - 1,200,000; Full time

Job summary

IQVIA is a leading global provider of clinical research services and healthcare intelligence. The Data Operations Coordinator role supports the Clinical Data Management team by delivering data management expertise, leading tasks, and ensuring quality outcomes for studies.

The position interacts with DOC, DTL, and the CDM team to meet client needs and project objectives. Based in India, the role may involve leadership activities under supervision and requires strong organizational and

Qualifications

• Bachelors degree in clinical, biological or mathematical sciences or related field.
• Equivalent education, training and experience considered.
• Excellent organizational, communication, leadership and computer skills.

Responsibilities

• Serve as a DOC for one protocol with fewer than 5 operations staff or 15+ easy to moderately complex central laboratory studies, or leadership role in 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.
• Understand and comply with SOPs and working instructions. Meet objectives and maintain good communications with the CDM team.

Education

Bachelors Degree in Clinical, Biological or Mathematical Sciences, or related field

Job description

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. Understand and comply with core operating procedures and working instructions. Meet objectives as assigned. Develop and maintain good communications and working relationships with CDM team."

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.