ICON is seeking experienced Clinical Research Associates (CRAs) to join our team in Mumbai and Delhi. As a CRA, you will play a key role in monitoring clinical trials and ensuring compliance with regulatory requirements.

Job Overview

Job Summary: ICON is hiring a Clinical Research Associate to support global biopharma studies in Mumbai and Delhi.

Company Profile: ICON is a global provider of outsourced development and commercialization services to pharmaceutical, biotechnology, medical device, and government and public health organizations. With offices in 40 countries, ICON has extensive experience in managing Phase I-IV clinical trials across a broad range of therapeutic areas.

Detailed Job Description

Responsibilities:

• Conduct on-site monitoring of clinical trials to ensure compliance with protocols, regulatory requirements, and good clinical practice (GCP).
• Manage clinical trial sites, including initiation, routine monitoring, and close-out visits.
• Submit documents to Institutional Review Boards (IRB) and ensure regulatory compliance throughout the trial.
• Communicate effectively with clinical trial investigators, coordinators, and other site staff.
• Maintain accurate and timely documentation of clinical trial activities.
• Review and verify case report forms and source documentation for accuracy and completeness.
• Ensure timely reporting of adverse events and protocol deviations.

Location

This role is based in Mumbai and Delhi, India. Travel to clinical trial sites within these regions will be required.

Basic Qualifications

• Minimum of a bachelor's degree in Pharmacy, Medicine, or related field (B.Pharm, M.Pharm, Pharm D, BDS, MBBS).
• At least 1 year of on-site monitoring experience in respiratory, cardiology, or nephrology studies.
• Strong understanding of clinical trial methodologies, GCP, and regulatory requirements.
• Excellent communication, organizational, and time-management skills.
• Ability to work independently and as part of a team.
• Proficient in Microsoft Office and clinical trial management software.

Preferred Qualifications

• Advanced degree (M.Pharm, MBBS) is preferred.
• Experience with electronic data capture (EDC) systems.
• Previous experience in a similar role within the biopharma industry.
• Strong analytical and problem-solving skills.
• Ability to travel frequently and manage multiple clinical trial sites.

How to Apply

Interested candidates are invited to apply by submitting their resume and cover letter.

Apply Online

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