Trial Coordinator

This role is ideal for highly specialized candidates holding a Post-Graduation in Science (Life Science, Biotech, etc.) combined with a P.G. Diploma in Clinical Research. Individuals with a keen interest in contributing to critical cancer research projects and those who possess a desirable 6 months of clinical research experience will find this role a good fit. The project-based, contractual nature suits those looking for focused, short-term engagements with potential for extension within a prestigious government institution.

Candidates lacking the mandatory Post-Graduation in Science and a P.G. Diploma in Clinical Research should not apply. Those seeking permanent government employment or higher-level administrative roles will find this specific contractual, project-based position unsuitable. Individuals requiring a guaranteed long-term tenure or a fixed pay scale beyond the consolidated amount may also find this role restrictive.

Working at ACTREC, a part of the Tata Memorial Centre and a Grant-in-aid Institution under the Dept. of Atomic Energy, offers significant prestige and exposure to advanced cancer research. While the role is contractual and for a single post, it provides invaluable experience in a leading research environment, enhancing a candidate's profile for future specialized roles in clinical research. The project focuses on a 'Phase 2 study to evaluate efficacy and safety of Lutetium-177 Rituximab', indicating involvement in cutting-edge medical trials.