Join ICON as a Clinical Research Associate in Delhi

Join ICON as a Clinical Research Associate in Delhi!
  • Full Time
  • delhi

Icon Hiring Clinical Research Associate – Onsite Monitoring: Unlock Your Career in Clinical Research with ICON

About the Company (ICON plc)

Welcome to ICON plc, a global healthcare intelligence and clinical research organization dedicated to advancing clinical research from molecule to medicine. With a focus on providing outsourced services to pharmaceutical, biotechnology, medical device, and government organizations, ICON is at the forefront of accelerating the development of drugs and devices that save lives and enhance the quality of life. Our commitment to patients, coupled with the passion and expertise of our people, makes ICON a leader in the industry.

Company Vacancies List

Position: Clinical Research Associate (CRA II)

  • Location: Delhi
  • Experience: 3+ years of onsite monitoring experience
  • Therapeutic Area: Oncology

If you are an experienced CRA looking for new opportunities or considering a move to Delhi, this is your chance to join our team. We are seeking dedicated professionals to contribute to our mission of advancing clinical research.

 Join ICON as a Clinical Research Associate in Delhi!
Join ICON as a Clinical Research Associate in Delhi!

Job Description

As a Clinical Research Associate at ICON, you will play a pivotal role in the successful management of investigator sites throughout the trial lifecycle. Key responsibilities include:

Full Ownership of Investigator Sites

  • Successfully manage investigator sites from initiation to close-out.

Site Visits

  • Plan and conduct various site visits, including feasibility, site selection, interim, and close-out, following the clinical monitoring plan.

Relationship Building

  • Develop effective relationships with investigator site staff to ensure key clinical metrics are met.

Investigator Meetings

  • Prepare for and attend investigator meetings, coordinate the timely shipment and proper storage of clinical supplies, and follow up on drug safety issues.

Clinical Data Integrity

  • Ensure the integrity of clinical data through the maintenance of site tracking records in accordance with relevant guidelines.

Trial Agreements

  • Negotiate and manage clinical trial agreements with investigative sites.

About the Department & Responsibilities

Our Clinical Operations team is unparalleled in its dedication to success. As a Clinical Research Associate, you will receive the support needed to develop both personally and professionally. Operating as a key part of a global study team, you will play a fundamental role in our clients’ drug development processes.

How to Apply

If you meet the requirements and are ready to take the next step in your clinical research career, follow these steps:

  1. Update your CV, highlighting your relevant experience.
  2. Email your CV to Abhisikta Mishra at
  3. Use the subject line “Clinical Research Associate Application.

Apply via Linkedin

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