Are you looking for exciting career opportunities in the healthcare and analytics domain? IQVIA, a global leader in healthcare data and analytics, is hiring for Data Analyst, Clinical SAS Programmer, and Clinical Trial Coordinator roles in Bangalore and Kolkata, India. These full-time positions offer a chance to work on cutting-edge projects, collaborate with global teams, and make a meaningful impact in the healthcare industry.
If you have a passion for data analytics, programming, or clinical research, this is your chance to join a world-class organization. Read on to learn more about the roles, responsibilities, and how to apply before the deadline on February 27, 2025.
1. Data Analyst Role at IQVIA
Location: Bangalore, India
Job Requisition ID: R1451949
Job Overview
As a Data Analyst at IQVIA, you will:
- Support recurring deliverables using PL/SQL, PySpark, SAS, Python, and BDF technologies.
- Contribute to ad-hoc projects and proof-of-concepts (POCs) as part of the US AA support team.
- Enhance your expertise in APLD (Anonymous Patient-Level Data) and the healthcare domain.
- Work on projects involving healthcare, retail, or banking analytics.
Key Responsibilities
- Manage 1-2 projects independently or as part of a team.
- Deliver projects related to healthcare analytics.
- Use tools like Excel, SAS, and PowerPoint for data analysis and presentation.
- Mentor junior team members and ensure quality checks.
- Develop domain knowledge in disease indications and market dynamics.
Essential Skills and Qualifications
- Proficiency in PL/SQL and experience with large databases.
- Strong analytical and problem-solving skills.
- Excellent communication skills (written and verbal).
- Knowledge of Python and basic understanding of UI development (HTML, CSS).
- Experience in healthcare, retail, or banking analytics is a plus.
2. Clinical SAS Programmer Role at IQVIA
Location: Kolkata and Bangalore, India
Job Requisition ID: R1466905
Job Overview
As a Clinical SAS Programmer, you will:
- Lead database design, development, and maintenance for clinical systems.
- Program, test, and document databases using Oracle, SAS, Python, and R.
- Mentor team members and collaborate with global teams.
- Drive process innovations and improvements.
Key Responsibilities
- Plan and coordinate database activities for clinical systems.
- Program database manipulations and data transfers.
- Collaborate with IT teams to implement new technologies.
- Ensure compliance with programming standards and validation procedures.
Qualifications
- Bachelor’s degree in Computer Science, Life Sciences, or related fields.
- 8+ years of experience in clinical data programming.
- Advanced knowledge of Oracle, SAS, Python, and R.
- Strong understanding of the clinical drug development process.
3. Clin Process Spec 2 Role at IQVIA
Location: Bangalore, India
Job Requisition ID: R1465714
Job Overview
Role: An exciting opportunity to contribute to the development of first-in-class specialty medicines for patients in need within our healthcare division. You will be part of an established team that supports study teams across Phase I to Phase IV (both interventional and non-interventional) and Investigator Sponsored Studies, with or without CRO involvement. As a Clinical Trial Coordinator, you will oversee activities within a dedicated Center of Excellence, ensuring the operational success of clinical studies while collaborating with multiple cross-functional teams and CROs.
Key Responsibilities
Responsibilities:
- Collaborate closely with clinical teams, offering support and specialized knowledge to ensure the successful and timely execution of clinical studies, while leveraging insights from senior leadership.
- Oversee and perform updates to the Clinical Trial Management System (CTMS) and associated databases, ensuring data integrity and compliance.
- Generate comprehensive reports, graphs, dashboards, newsletters, and data models to facilitate team meetings and enhance the decision-making process.
- Analyze diverse data sets, identify emerging data types, and synthesize information into actionable metrics and insights.
- Monitor data quality, proactively identify inconsistencies and risks, and implement corrective actions.
- Manage system access and ensure appropriate oversight of study resources, optimizing resource allocation and usage.
- Assisting and mentoring junior staff
Qualifications:
- Graduate background (e.g. Bachelor’s degree) in scientific field plus substantial relevant professional experience (5 years or more in Clinical Development or equivalent) and very good knowledge and experience in own discipline and beyond
- Exceptional oral and written communication skills in English.
- Proven ability to thrive in an international, multicultural, and cross-functional matrix environment.
- Strong understanding of Clinical Operations policies and procedures, as well as ICH-GCP guidelines.
- Proficient in utilizing CTMS across all functionalities, ideally as a CTMS Super User.
- Highly experienced in generating reports from various IT systems, such as CTMS and Spotfire.
- Capable of effectively collecting and analyzing large-scale data sets from various sources for reporting purposes.
- Excellent qualitative and quantitative analytical skills.
- Ability to streamline and automate processes for increased efficiency.
- Proficient in computer skills, including advanced knowledge of MS Office™ (Word™, PowerPoint™), Outlook, and TEAMS.
- Highly experienced in Excel™, including Text, Date & Time, Lookup & Reference, Statistical Functions, and Pivot Tables.
- Strong administrative, coordination, and problem-solving abilities.
- Excellent time management and prioritization skills, with the capacity to work independently and efficiently under pressure.
Why Join IQVIA?
- Work on innovative projects in the healthcare and analytics domain.
- Collaborate with global teams and gain exposure to cutting-edge technologies.
- Enjoy a supportive work environment with opportunities for professional growth.
- Contribute to the development of first-in-class specialty medicines for patients in need.
How to Apply
Don’t miss this opportunity to join IQVIA! Apply before the deadline on February 27, 2025.
- Data Analyst Role: Apply Here
- Clinical SAS Programmer Role: Apply Here
- Clin Process Spec 2 Role: Apply Here
