Clinical Research

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.

Bachelors degree in Life Sciences, Pharmacy, Medicine, or related field, with a keen interest in medical writing, clinical research, and drug development processes. Excellent written and verbal communication skills, with the ability to translate complex medical and scientific information into clear, concise, and engaging content tailored to diverse audiences.

Responsible to monitors activities at clinical study sites to assure adherence to Good Clinical Practices GCPs, Standard Operating Procedures, and study protocols under supervision of Clinical Operations Manager, Clinical Research Specialist.

Post Graduate Diploma in Clinical Trials or equivalent with at least 60% marks. At least one-year experience in clinical research. Experience in recruiting patients in clinical trials, familiarity with good documentation practices and good clinical practices.

Ensures that direct reports have development and training plans, according to IDP process. Coaches the direct reports on a regular basis, and plans, organizes coaching with external providers if needed.