Associate Clinical Data coordinator

IQVIA; Bengaluru; On-site; INR 300,000 - 450,000; Full time

Job summary

IQVIA is looking for an Associate Clinical Data Coordinator in Bengaluru. The ideal candidate will assist the Data Manager in various data management projects, ensuring clean data quality and timely deliverables. Responsibilities include project management and regular interaction with team leaders for quality assurance.

Applicants should possess a Bachelor's Degree in Science or Pharmacy, fluency in English, and basic computer skills. The position is office-based, promoting collaboration with teams for effective data management.

Qualifications

• Bachelor’s Degree in Science or Bachelor of Pharmacy or equivalent.
• Fluency in spoken and written English is essential.
• Basic proficiency in Microsoft Office applications.

Responsibilities

• Assist the Data Manager in managing data management projects.
• Perform regular data cleaning to ensure data quality.
• Interact with the Data Management team leaders.

Skills

English fluency (spoken and written)

Basic computer applications (Excel, Word, Outlook)

Understanding of drug development lifecycle

Education

Bachelor’s Degree in Science or Bachelor of Pharmacy or equivalent

Job description

Overview

Job title: Associate Clinical Data Coordinator

Experience: 1.5 to 3 years

Location: Kochi and Bangalore

Mode of work: Office based

Job Overview: Support Data Manager in managing data management projects as per sponsor requirements and coordinate with other departments, sites and sponsors as necessary.

Responsibilities

• Perform/Assist the Data Manager in managing various data management projects as per sponsor requirements and to provide efficient, quality management products. Support coordinate with other departments, sites and sponsors as necessary.
• Perform/Assist regular data cleaning activities to ensure clean data with quality and timely deliverables to sponsors.
• Serve in the role of back-up to a Sr. Data Coordinator or Data Team Lead.
• Manage the allocated tasks with minimum oversight.
• Ensure that all the deliverables are of expected quality standards and meet customer expectations with support of Senior Data Manager.
• Interact with Data Management team leaders to report on the quality of data collection and tasks done.
• Attend internal study meetings and internal/sponsor audits.
• Assist in tracking and managing the projects, oversee project progress, identify risks and take corrective action to rectify any errors as recommended by DT.
• Be compliant with trainings and eSOP reading.
• Communication with Data Team Lead and other team members across functions should be collaborative.

Qualifications

• Bachelor’s Degree in Science or Bachelor of Pharmacy or equivalent.
• English fluency (spoken and written).
• Basic computer applications such as Microsoft Excel, Word, and Outlook.
• Basic understanding of the drug development lifecycle and overall clinical research process.