Sr Clin Data Coordinator

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

Job summary

IQVIA LLC is seeking a Senior Data Coordinator in India to lead data management activities across allocated complex studies. The role involves acting as the main DM contact, ensuring data quality, and coordinating with sponsor audits and study timelines.

You will mentor teammates and contribute to new technology implementations. Qualifications include a Bachelor's in clinical/biological sciences and strong MS Office/Excel skills, with 4.8+ years in CDM.

Qualifications

• Bachelor's degree in clinical, biological or mathematical sciences, or related field.
• Clinical Data Management experience or equivalent combination of education, training and experience.
• Excellent organizational, communication and computer skills.
• Ability to act independently and with initiative to resolve problems.
• Knowledge of MS Office, Word and Excel; internet usage; macro knowledge helpful.

Responsibilities

• Lead DM and main contact for projects managed by the team.
• Ensure deliverables meet quality standards and customer expectations.
• Attend study kick-off meetings and sponsor audits for assigned studies.
• Report data quality and site issues to Data Management Team Leaders and update on project status.
• Mentor team members and ensure required trainings are completed.
• Assist in developing and implementing new technology/database revisions.

Skills

Lead DM

Project coordination

Attention to detail

MS Office

Excel

Communication

Audits

Mentoring

Data cleaning

Education

Bachelor's in clinical/biological sciences

Job description

## Sr Clin Data CoordinatorApply: Kolkata, West Bengal, India: Bangalore, India: Full time: Posted Today: End Date: October 6, 2026 (5 days left to apply): R1562663Job OverviewServe 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 clientsIQVIA 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.comIQVIA 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.