PHARMAFull-time
Centralized Site Assistant
THANE (IN)ONSITEPOSTED: 7/17/2026
PHARMAFull-time
HIRING ORGANIZATIONIQVIAHealthcare Technology & Contract Research
ROLE DEFINITION & RESPONSIBILITIES
Key Responsibilities
Support Clinical Study Management teams with administrative activities
Prepare study reports and trackers
Maintain project databases and compliance systems
Generate study status reports
Prepare i-site packs
Support access management requests
Assist Technical Solution Specialists using Microsoft Excel
Review Key Risk Indicators (KRIs)
Identify potential site risks
Recommend corrective actions
Participate in project meetings
Support Central Monitoring activities
Eligibility
Graduate or Postgraduate degree in Life Sciences
Minimum 2 years overall experience
At least 6 months of relevant Clinical Research experience
Knowledge of: ICH-GCP, Clinical Research regulations, Microsoft Excel, Word, PowerPoint
Good communication skills
Strong attention to detail
REQUIRED VERIFIED SKILLS
ICH-GCP
Clinical Research regulations
Microsoft Excel
Word
PowerPoint
COMPENSATION & REWARDS
₹4.0L - 6.5L per annum
The estimated annual salary for this role ranges from ₹4 to ₹6.5 LPA. The actual compensation package is competitive and depends significantly on the candidate's total experience, technical skills, and performance during the interview process.
ORGANIZATION CONTEXT & CULTURE
IQVIA is a leading global provider of advanced analytics, technology solutions, and contract research services (CRO) to the life sciences industry. The company helps pharmaceutical, biotech, and medical device clients accelerate the development and commercialization of new medical treatments through its extensive data, technology, and human expertise. Their offerings span from clinical trial design and execution to real-world evidence and commercial effectiveness.
TEAM SIZE: 87,000+ employees
INDUSTRY: Healthcare Technology & Contract Research
EXPECTED CAREER ROADMAP
IQVIA offers exceptional career progression opportunities within centralized clinical operations. Professionals gain exposure to international projects, advanced clinical technologies, and global clinical research standards, paving the way for advanced roles in clinical trial management.
APPLICATION ADVISORY
Candidates should emphasize their 6+ months of clinical research experience and demonstrate strong proficiency in Microsoft Excel and ICH-GCP guidelines. Highlighting attention to detail and strong administrative support capabilities will help stand out.
RECOMMENDED TRAINING
1/5
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