Q

Quanticate

Clinical data management and analysis services

Clinical Data Coordinator 2

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeBengaluru, Karnataka, IndiaNo salary listedIn-person

About the Job

Requirements

  • Strong understanding of Clinical Data Management processes.
  • Solid knowledge of ICH-GCP guidelines and regulatory requirements related to data handling.
  • Familiarity with CRO and sponsor-driven study standards.
  • Prior experience in Clinical Data Management or a similar role.
  • Hands-on experience with at least one Clinical Data Management system, such as Oracle Clinical, Medidata Rave, or Inform.
  • Excellent attention to detail and strong analytical thinking.
  • Good written and verbal communication skills.
  • Strong organizational and time-management abilities.
  • Ability to work effectively in a fast-changing, deadline-driven environment.
  • Comfortable working with offshore or remote teams.
  • Proficient in Microsoft Word and Excel.
  • Team-oriented mindset with the ability to motivate and collaborate effectively.

Responsibilities

  • Support end-to-end Clinical Data Management activities across multiple studies.
  • Assist with database testing and validation prior to study activation.
  • Prepare and maintain study-specific Data Management documentation.
  • Review CRFs critically, identifying data inconsistencies, errors, or missing information.
  • Raise, track, and resolve data queries and Data Clarification Forms (DCFs).
  • Manage self-evident queries and allowable data changes within the database.
  • Perform quality control checks on data entry and database outputs.
  • Support study close-out activities, including preparation of archival documentation.
  • Ensure compliance with SOPs, ICH-GCP, regulatory requirements, and client standards.
  • Contribute to process improvement initiatives and data management best practices.
  • Perform medical coding activities when assigned.
  • Collaborate with offshore data processing and programming teams.
  • Provide project updates and support progress tracking using reports and metrics.
  • Take on ad-hoc tasks as required to support project and team objectives.

Desired Qualifications

  • Experience supporting multiple studies or managing competing priorities.

About the Company

Quanticate

Clinical data management and analysis services

Quanticate is a global data-focused clinical research organization that supports pharmaceutical, biotechnology, and medical device companies with the data side of clinical trials, including Clinical Data Management, Biostatistics, SAS Programming, data quality oversight, Medical Writing, and Pharmacovigilance. It works by deploying staff to manage trial data—cleaning and organizing it, running statistical analyses, writing reports, and monitoring quality—delivered through flexible models like study-level support, functional service provision, strategic full data-services, or technical consulting. The company differentiates itself with a data-first approach, deep specialization across the data lifecycle, global reach, and adaptable engagement options tailored to each trial. Its goal is to be the supplier of choice for data-driven clinical research by delivering accurate, timely, and compliant data solutions that speed up and improve decision-making in trials.

Company size
201-500
Company stage
Not listed
Total funding
Not listed
Headquarters
Hitchin, United Kingdom
Founded
1994

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