Clinical Research Associate

Job Overview

Join Sun Pharmaceutical Industries Ltd as a Clinical Research Associate based in Mumbai, India. This role involves monitoring clinical trial sites to ensure adherence to regulatory standards, study protocols, and company expectations.

Primary Responsibilities

• Perform site monitoring visits to verify compliance with applicable regulations, study protocols, and corporate policies.
• Work closely with investigators, sponsors, and contract research organizations (CROs) to address and resolve issues encountered during clinical trials.
• Compile detailed study reports covering findings such as adverse events (AEs) and serious adverse events (SAEs), alongside other pertinent clinical data.
• Manage timely submission of essential documentation including case report forms (CRFs) and responses to queries.

Qualifications and Requirements

• Between three to five years of professional experience in clinical research or allied disciplines.
• Comprehensive knowledge of International Council for Harmonisation Good Clinical Practice (ICH-GCP) guidelines and regulatory requirements pertinent to clinical studies.
• Strong communication skills facilitating collaboration with multidisciplinary teams.

Eligibility

Candidates holding degrees such as B.Sc or other graduate qualifications are eligible to apply.