IQVIA Hiring Site Report Specialist

Be at the Forefront of Healthcare Innovation: Join IQVIA

Are you passionate about clinical research and healthcare advancements? IQVIA, a global leader in healthcare technology and innovation, is seeking skilled professionals for the role of Site Report Specialist. This is your chance to contribute to groundbreaking clinical trials and work with industry experts in a dynamic, supportive environment.

Job Overview

Position: Site Report Specialist

• Location: Mumbai, Bangalore
• Experience Required: Minimum 4+ years in clinical research
• Education Qualification: Relevant qualifications in life sciences, clinical research, or a related field

Key Responsibilities

• Onsite Monitoring: Manage and oversee onsite clinical trial activities to ensure compliance with protocols and regulations.
• Clinical Trial Oversight: Work on clinical trials, primarily in Phases 2 and 3, ensuring accurate data collection and reporting.
• Collaboration: Collaborate with Clinical Research Associates (CRAs), Clinical Trial Assistants (CTAs), and Clinical Research Coordinators (CRCs) to streamline processes.
• Reporting: Create detailed site reports to track trial progress, identify challenges, and propose solutions.

Skills and Qualifications

Essential Skills

• Minimum 4+ years of experience in a clinical research role.
• At least 3+ years of onsite monitoring experience.
• Background in CRA, CTA, or CRC roles.
• Expertise in managing clinical trials during Phases 2 and 3.

Additional Skills

• Excellent communication and organizational abilities.
• Strong knowledge of clinical trial regulations and protocols.
• Problem-solving skills to address trial-related challenges effectively.

How to Apply

Interested candidates are invited to share their resumes at:
📧 Email: priyanka.tyagi2@iqvia.com

Tagged as: Good Clinical Practice (GCP)