Clinical Research

Developing Precision Immunotheraphy for Value –Based Treatment of Lung Cancer in India. Graduate, Post Graduate in Life Science with a Diploma in clinical Research. MSC in Clinical Research. 1 - 2 years of experience in Project Management is Mandatory. Experience in drafting of study progress and fund utilization reports is Desirable.

First-class in Masters in Clinical Research, Clinical Trials including an integrated masters degree, or Second class in Masters in Clinical Research, Clinical Trials including an integrated Masters degree with a PhD in Clinical Research, Clinical Trials, Epidemiology.

An open–label phase II trial evaluating the activity and safety of JDQ443 single agent as first-line treatment for patients with locally advanced or metastatic KRAS G12Cmutated non-small cell lung cancer

Applications are invited for the post of Clinical Research Coordinator in different drug trials. The following are the educational qualifications/salary for this post.

Improving Survival in Childhood Acute Lymphoblastic Leukemia in India ISCALL ICICLE IMPLEMENTATION STUDY. Graduation in Science B.Pharm, Life Science, B.Sc. Biotech, Zoology, Botany, etc with PG Diploma in Clinical Research with three years experience or PG in the relevant subject, field.

To support the teaching needs of the M.Sc. in Clinical Research program with a specialization in Clinical Trials at THSTI.  Contribute ongoing and future clinical trials, epidemiological studies, and other health- related research projects by providing robust statistical expertise.

Post Graduation in Science M.Pharm, Life Sciences, Biotech, Zoology, Botany, etc. With PG Diploma in Clinical Research is mandatory. Candidates should have at least one-year experience as Clinical Trial / Research Coordinator is mandatory.

Bachelor’s in science, Pharmacy B.Pharm with degree, diploma in Clinical Research Methodology. The candidate with a minimum 1 year experience in conducting clinical trial will be given preference.

The Clinical Research Lead will oversee and manage clinical research activities within the organization. This role involves designing, implementing, and monitoring clinical trials to ensure they meet regulatory requirements and organizational goals.