Sr Clin Data Coordinator

IQVIA Inc; Bengaluru; On-site; INR 1,800,000 - 3,000,000; Full time

Job summary

IQVIA is seeking a Senior Data Coordinator to oversee allocated complex studies within the Clinical Data Management (CDM) domain. The role acts as a DM lead and primary contact for multiple projects, ensuring timely, accurate data delivery and adherence to sponsor specifications.

The ideal candidate will manage study start-up to close-out activities, participate in kick-offs and audits, and mentor junior staff while implementing new database revisions and technologies.

Qualifications

• Bachelor's degree in clinical, biological or mathematical sciences is required
• Clinical Data Management or equivalent combination of education, training and experience is required
• Excellent organizational, communication and computer skills with strong attention to detail
• Ability to act independently and with initiative to resolve problems
• Knowledge of MS Office, Word and Excel
• Internet usage and clinical application programming/macro knowledge is helpful
• Ability to establish and maintain effective working relationships with coworkers, managers and clients

Responsibilities

• Serve as Senior Data Coordinator for allocated complex studies and lead a DM task
• Lead DM projects and be the main point of contact for team
• Ensure all deliverables meet quality standards and client expectations
• Attend study kick-off meetings and sponsor audits for assigned studies
• Report on data quality and site issues to Data Management Team Leaders and update status
• Interact with CDM personnel for timelines and data delivery
• Ensure data cleaning, data transfer to sponsor per specs, and proper archiving at study end
• Mentor team members and ensure trainings are completed
• Assist in developing and implementing new technology/database revisions

Skills

Attention to detail

Organizational skills

Communication skills

Initiative

Independent work

Education

Bachelor's degree in Clinical, biological or mathematical sciences

Tools

MS Office

Word

Excel

Job description

Job Description:

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.

Requirements: