IQVIA Hiring Pharma Graduates | Assoc Clinical Data Coord Role – Apply Now
Looking for a CDM Job in the clinical research industry? IQVIA Careers is hiring an Associate Clinical Data Coordinator in Bengaluru. This opportunity is ideal for Science and B.Pharm graduates who want to build a career in clinical data management, data cleaning, and clinical research while working with one of the world’s leading healthcare intelligence companies.
- Job Title: Assoc Clinical Data Coord
- Job Reference: R1560211
- Location: Bengaluru, India
About The Company
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. The organization is dedicated to creating intelligent connections that accelerate the development and commercialization of innovative medical treatments, ultimately improving patient outcomes and population health worldwide. The company is headquartered in Durham, North Carolina, USA, and operates in numerous countries, including India.
Job Description
IQVIA Careers is hiring an Associate Clinical Data Coordinator to support clinical data management projects. The Assoc Clinical Data Coord role involves assisting in regular data cleaning activities to ensure clean data with quality and timely deliverables to sponsors. The candidate will serve as a back-up to a Senior Data Coordinator or Data Team Lead and manage allocated tasks with minimal oversight. Ensuring that all deliverables meet expected quality standards and customer expectations is crucial, with support from the Senior Data Manager. The role also includes interacting with Data Management team leaders to report on data quality, attending internal study meetings, and assisting in tracking and managing projects.
Key Responsibilities
- Perform/Assist regular data cleaning activities to ensure clean data with quality and timely deliverables to sponsors.
- Serve as a back-up to a Senior Data Coordinator or Data Team Lead.
- Manage allocated tasks with minimal oversight.
- Ensure deliverables meet expected quality standards and customer expectations.
- Interact with Data Management team leaders regarding data collection quality.
- Attend internal study meetings and internal/sponsor audits.
- Assist in tracking and managing projects, overseeing progress, and identifying risks.
- Maintain compliance with training and eSOP reading.
Eligibility Criteria
- Education: Bachelor’s Degree in Science/Bachelor of Pharmacy or equivalent preferred.
- Experience: Basic proficiency in computer applications such as Microsoft Excel and Word. Understanding of the drug development lifecycle and overall clinical research process.
Required Skills
- Clinical Data Management (CDM)
- Data Cleaning
- Clinical Research Knowledge
- Drug Development Lifecycle
- Microsoft Excel & Word
- Data Quality Management
- Project Coordination
- Risk Identification
- Communication Skills
- Team Collaboration
Why Join IQVIA?
Joining IQVIA Careers offers an excellent opportunity to gain hands-on experience in clinical data management, research operations, and global clinical trials. This CDM Job provides exposure to international projects, structured learning, and career growth in one of the world’s leading clinical research organizations.
Pharmanika is a career information portal. Please verify all details from the original notification before applying.
