IQVIA, a global leader in clinical research and healthcare intelligence, is hiring a Clinical Research Associate (CRA 2) for its Thane, Maharashtra location. This is an excellent opportunity for professionals with at least 1 year of on-site monitoring experience to advance their careers in clinical research.
Key Responsibilities
As a Clinical Research Associate (CRA), you will be responsible for:
- ConductingΒ site monitoring visitsΒ (selection, initiation, monitoring, and close-out) in compliance withΒ GCP, ICH guidelines, and sponsor requirements.
- Training site staff onΒ study protocolsΒ and ensuring adherence to regulatory standards.
- Tracking study progress, including regulatory approvals, patient recruitment, and data reporting.
- Ensuring properΒ documentationΒ in theΒ Trial Master File (TMF)Β andΒ Investigatorβs Site File (ISF).
- ManagingΒ site relationshipsΒ and resolving study-related issues efficiently.
- SupportingΒ subject recruitment strategiesΒ to meet project timelines.
- HandlingΒ site financial managementΒ as per clinical trial agreements (if applicable).
Qualifications & Skills Required
- Bachelorβs degreeΒ in a scientific or healthcare-related field (preferred).
- Minimum 1 year of on-site monitoring experienceΒ in clinical research.
- Strong knowledge ofΒ GCP, ICH guidelines, and regulatory requirements.
- Proficiency inΒ Microsoft Office (Word, Excel, PowerPoint)Β and electronic data capture systems.
- ExcellentΒ communication, organizational, and problem-solving skills.
- Ability to manageΒ time and site budgetsΒ effectively.
About IQVIA
IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. With a focus on improving patient outcomes, IQVIA delivers intelligent healthcare solutions that accelerate drug development and commercialization.
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How to Apply
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