MBBS

Master degree in Pharmacy, Clinical Pharmacology, Pharmacy Practice, and Clinical Research preferably with diploma in clinical research from the recognised institute.

Conduct site monitoring visits from initiation through closeout, ensuring trials are conducted in compliance with the study protocol, GCP guidelines, SOPs, and applicable regulatory requirements. Set up trial sites, ensuring that investigational products and essential trial supplies are delivered, stored, and documented appropriately.

Aspiring interns should be in the pre-final or final year of their Masters M.E, M.Tech, M.Sc or Bachelors degree course B.E, B.Tech, B.Sc in India in Life Sciences, Biotechnology, that are relevant to the research projects at CBR.

Online Applications are invited for various posts as under NATIONAL CANCER GRID - NCG. Candidates who would be called for Interview are required to carry original documents in support of the details furnished in the online application form regarding date of birth, qualifications, experience, etc., failing which such applicants will not be allowed to appear for Interview. 

Act as an interface with identified scientific leaders, building regional relationships to contribute to understanding diseases, research trends, clinical practice guidelines, and treatment patterns. Educate healthcare professionals about specific drugs or medical devices, answering their scientific questions and ensuring products are used effectively.

Provide medical and scientific training to internal stakeholders, including the sales and marketing teams, ensuring accuracy and alignment with scientific evidence. Collaborate with cross-functional teams to support the development of strategic initiatives in line with medical and commercial objectives.

Professional having B.Pharm, BAMS, B-Tech, MPH. Preference will be given to professionals having experience in Digital Health. Foster partnerships with academia, industry, and international organization to accelerate digital health adoption.

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.

BPharm, BSc, MPharm, MSc, MBBS, BAMS; Experience in PV/ Clinical Research drug safety preferred. Ability to understand and analyses the complex data and performs the activities including accessing the case in Argus, code and enter data.