IQVIA Job Openings for Multiple Positions – Apply Now!
Are you looking for an exciting career opportunity in the life sciences industry? IQVIA, a global leader in healthcare data, analytics, and technology, is hiring for multiple positions across India. This is your chance to be part of a dynamic team that is transforming healthcare. Below, you will find detailed information about each job opening and how to apply.
Senior Statistical Programmer – Hyderabad, Telangana, India
Job Description
We are seeking a highly skilled Senior Statistical Programmer to join our team in Hyderabad. In this role, you will be responsible for developing and validating SAS programs for data analysis, report generation, and data submission. You will work closely with statisticians, data managers, and other programmers to ensure the quality and accuracy of our data.
Key Responsibilities
- Develop and validate SAS programs for clinical trials data analysis
- Generate tables, listings, and figures for clinical study reports
- Ensure compliance with regulatory requirements and guidelines
- Collaborate with cross-functional teams to meet project deadlines
- Provide technical support and training to junior programmers
Qualifications
- Bachelor’s degree in Statistics, Computer Science, or a related field
- Minimum of 5 years of experience in statistical programming
- Proficiency in SAS programming and data management
- Strong understanding of clinical trials and regulatory requirements
- Excellent problem-solving and communication skills
How to Apply
click here to apply for above postion
Senior Analyst, Regulatory Intelligence – Bengaluru, Karnataka, India
Job Description
IQVIA is looking for a Senior Analyst, Regulatory Intelligence to join our team in Bengaluru. This position involves monitoring and analyzing global regulatory developments and providing insights to support our clients’ regulatory strategies. You will be a key contributor to our regulatory intelligence team, helping to shape the future of healthcare compliance.
Key Responsibilities
- Monitor and analyze global regulatory developments and trends
- Provide strategic insights and recommendations to clients
- Prepare detailed regulatory intelligence reports and presentations
- Collaborate with internal teams to support regulatory compliance efforts
- Stay up-to-date with changes in regulatory guidelines and standards
Qualifications
- Bachelor’s degree in Life Sciences, Pharmacy, or a related field
- Minimum of 4 years of experience in regulatory affairs or regulatory intelligence
- Strong analytical and research skills
- Excellent written and verbal communication skills
- Ability to work independently and as part of a team
How to Apply
click here to apply for above postion
Senior Dataware Developer – Kochi, Kerala, India
Job Description
We are looking for an experienced Senior Dataware Developer to join our team in Kochi. In this role, you will design, develop, and maintain data warehouses to support our business intelligence and analytics initiatives. You will work with large datasets and create efficient data models to facilitate data-driven decision-making.
Key Responsibilities
- Design and develop data warehouses and ETL processes
- Create and maintain data models and schemas
- Optimize data storage and retrieval for performance
- Collaborate with business analysts and data scientists to understand data needs
- Ensure data quality and integrity across all systems
Qualifications
- Bachelor’s degree in Computer Science, Information Technology, or a related field
- Minimum of 5 years of experience in data warehousing and ETL development
- Proficiency in SQL, Python, and data modeling tools
- Strong understanding of data warehousing concepts and best practices
- Excellent problem-solving and analytical skills
How to Apply
click here to apply for above postion
Associate Project Manager – Kochi, Kerala, India
Job Description
IQVIA is seeking an Associate Project Manager to join our team in Kochi. This role involves managing and coordinating projects related to clinical trials, data management, and regulatory compliance. You will ensure that projects are completed on time, within scope, and within budget while meeting high-quality standards.
Key Responsibilities
- Manage and coordinate clinical trial and data management projects
- Develop project plans, timelines, and budgets
- Monitor project progress and address any issues that arise
- Communicate with clients and stakeholders to ensure project alignment
- Ensure compliance with regulatory requirements and company standards
Qualifications
- Bachelor’s degree in Life Sciences, Project Management, or a related field
- Minimum of 3 years of experience in project management
- Strong organizational and multitasking skills
- Excellent communication and leadership abilities
- Knowledge of clinical trials and regulatory processes
How to Apply
click here to apply for above postion
Join IQVIA and be part of a team that is driving innovation in healthcare. Apply now and take the next step in your career!
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