Job Description
This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Central Report Reviewer based in India.
In this role, you will play a critical part in ensuring the quality, consistency, and compliance of clinical trial reporting activities across global studies. You will review central monitoring documentation and site-level reports to ensure accuracy, completeness, and alignment with GCP, protocol requirements, and patient safety standards. The position is highly detail-oriented and contributes directly to safeguarding data integrity and regulatory compliance in clinical research. You will collaborate closely with clinical operations teams, including CRAs, Clinical Trial Managers, and project stakeholders, to identify risks and escalate issues when necessary. This role operates in a fast-paced, global environment where precision, scientific rigor, and communication are essential. You will also contribute to continuous improvement by identifying trends, reporting quality gaps, and supporting monitoring strategy execution across studies. The work directly supports the advancement of clinical trials and ultimately the delivery of new therapies to patients worldwide.
This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Central Report Reviewer based in India.
In this role, you will play a critical part in ensuring the quality, consistency, and compliance of clinical trial reporting activities across global studies. You will review central monitoring documentation and site-level reports to ensure accuracy, completeness, and alignment with GCP, protocol requirements, and patient safety standards. The position is highly detail-oriented and contributes directly to safeguarding data integrity and regulatory compliance in clinical research. You will collaborate closely with clinical operations teams, including CRAs, Clinical Trial Managers, and project stakeholders, to identify risks and escalate issues when necessary. This role operates in a fast-paced, global environment where precision, scientific rigor, and communication are essential. You will also contribute to continuous improvement by identifying trends, reporting quality gaps, and supporting monitoring strategy execution across studies. The work directly supports the advancement of clinical trials and ultimately the delivery of new therapies to patients worldwide.