Sr Clin Data Coordinator

IQVIA; Kolkata District; On-site; INR 900,000 - 1,300,000; Full time

Job summary

IQVIA is seeking a Senior Data Coordinator to lead data management for allocated complex studies in India (Kolkata/Bangalore). You will act as the main DM contact, ensure timely, high-quality data deliverables, and support audits and study kick-offs.

The role requires strong organizational skills, independence, and mentoring junior staff. The ideal candidate has 4.8+ years in CDM, excellent communication, and proficiency with MS Office and clinical data systems.

Qualifications

• Bachelor's Degree in clinical, biological or mathematical sciences or related field.
• 4.8+ years in end-to-end CDM processes.
• Strong organizational and communication skills.
• Able to work independently and proactively resolve problems.
• MS Office proficiency; data management tools familiarity.

Responsibilities

• Lead data management activities for allocated complex studies.
• Be main contact for projects; ensure deliverables meet quality standards.
• Attend study kick-off meetings and audits.
• Report data quality and site issues to team leaders.
• Coordinate timelines and provide project updates.
• Ensure data is cleaned and archived at study end.
• Mentor team members and support trainings.
• Assist in implementing new tech/database revisions.

Skills

Clinical Data Management

Lead DM

Data quality

Project coordination

MS Office

Communication

Education

Bachelor's Degree in Clinical/ Biological/ Mathematical Sciences

Tools

MS Word

MS Excel

Clinical data systems

Job description

Kolkata, West Bengal, India

Bangalore, India

Full time

R1562663

Job Overview

Serve as Senior Data Coordinator for allocated complex studies and serve in a leadership role to a specific DM Task.

Essential Functions

• Minimum of 4.8 years of relevant industry experience in end-to-end Clinical Data Management (CDM) processes is required, including study start-up, study conduct, and study close-out activities.
• Serve as a lead DM and the main point of contact for various projects managed by the team.
• Ensure that all the deliverables are of expected quality standards and meet customer expectations
• Attend study kick off meetings and internal/sponsor audits for assigned studies.
• Report on the quality of data collection and site issues to Data Management Team Leaders and apprise them of the status of each project.
• Interact with the Clinical Data Management personnel for project timelines, delivery of quality data and frequent project update teleconferences.
• Ensure that at the end of the study, all the Data Clarification forms are resolved, all data is “cleaned”, the data transfer is sent to the sponsor as per the agreed specifications, the data and the study files are completed and archived appropriately.
• Mentor other team members and ensure the completion of all required trainings .
• Assist in developing and implementing new technology / database revisions.

Qualifications

• Bachelor's Degree Clinical, biological or mathematical sciences, or related field Req
• Clinical Data Management or Equivalent combination of education, training and experience in lieu of degree. Req
• Excellent organizational, communication and computer skills. Ability to exercise excellent attention to detail
• Ability to act independently and with initiative required to resolving problems.
• Knowledge of Computer application- MS Office, Word and Excel
• Internet usage, Clinical application Programming /Macro knowledge will be helpful
• 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.

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

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

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