Recruitment for Master Professional as Scientist at National Institute of Medical Statistics - PG or Ph.D in Pharmacology

The Clinical Trials Registry - India (CTRI) is an online system for registration of all clinical trials being conducted in the country. This web based system (ctri.nic.in) has its headquarters at the National Institute of Medical Statistics (NIMS), Indian Council of Medical Research (ICMR). It serves as a platform for registering all clinical trials on health products including drugs, devices, vaccines, herbal drugs etc. The registration of trials in CTRI is free of cost and crucial information of these registered clinical trials is freely searchable from the CTRI site. The CTRI currently registers interventional trials as well as BA/BE and observational studies. While the mandate is to register trials prospectively, the CTRI also registers ongoing and completed trials. The primary objective of the registry is to enhance transparency, accountability and accessibility of clinical trials and their results. However, there are several other benefits as well.

Post : Scientist C (One)

Qualification (Essential)
Post graduate degree (MD/MS/DNB) after MBBS with one year experience
OR Postgraduate diploma in medical subjects after MBBS with two years’ experience
OR MBBS Degree with four years’ experience in medical subjects after MBBS Degree
OR Ist Class Post Graduate degree and Ph.D in Pharmacology/Toxicology/Biological /Life Sciences/ Biotechnology from a recognized University
OR Ist Class Post Graduate degree in Pharmacology/Toxicology/Biological /Life Sciences/ Biotechnology from a recognized University along with 4 years R&D experience in the required subject.
OR Second class Master’s Degree in any of the above subjects along with Ph.D. degree from a recognized university or equivalent.
OR BDS degree recognized by DCI with five years’ experience in relevant subject after BDS degree.

 

Desirable
Experience in Clinical Research. Good English writing skills, knowledge of clinical trials and drug regulatory procedures.

Job Description : To review, compile data on clinical trials, report writing and handling tasks as assigned in the Clinical Trials Registry – India.

Emoluments (pm) : Rs.64000/-plus HRA (Medical) Rs. 51000/- plus HRA (Non-medical)

Age :  Not exceeding 40 years. Relaxable up to 5 years for Government servants and SC/ST/OBC candidates.

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