Full-Time
Salary: 25k to 30k
Positions: 10

Pharmacovigilance Services Associate

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Job Description

 Location: Bangalore, Bengaluru
Job ID: JR137250
Category: Clinical Trial Support | ICON Full Service & Corporate Support

Work Type: Office Based

About the Role

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment that drives innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

We are currently seeking a Clinical Trial Associate (CTA) to join our diverse and dynamic team. As a CTA at ICON, you will play a pivotal role in coordinating and supporting the operational aspects of clinical trials  ensuring compliance, accuracy, and efficiency throughout the study lifecycle.

Role & Responsibilities

  • Assist in the coordination and administration of clinical trials in accordance with protocols and regulatory requirements.
  • Maintain and organize essential clinical trial documentation, including study files and regulatory submissions.
  • Support the preparation of study-related materials such as informed consent forms and case report forms.
  • Collaborate with cross-functional teams to ensure effective communication and smooth trial execution.
  • Contribute to the tracking and reporting of clinical trial progress, timelines, and milestones.

Educational Qualification

  • Bachelor’s degree in a scientific or healthcare-related field.
  • Prior experience or strong interest in clinical research.
  • Good understanding of clinical trial processes, ICH-GCP guidelines, and regulatory practices.
  • Strong organizational, analytical, and communication skills.
  • Ability to work collaboratively in a fast-paced and dynamic environment.
  • Attention to detail and accuracy in documentation and data handling.

Location

Bangalore, Bengaluru

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