department of health research announced job notification for the positions of consultant in the department of and in section of clinical trials training guidelines, . This job position consultant located in and in state delhi. This job position is categorized as '' jobs.

The educational qualifications for this job position consultant specified as A person having M.D. /M.S. Degree in medical subjects or 1st class Master Degree in Life science. Eligibility conditions for job position consultant mentioned as and required experience levels for this job position consultant are as follows minimum 10 years of experience. Adequate experience in handling research projects and formulating policy/Strategy documents.

The salary or payscale for consultant is Rs.80,000 - 1,00,000.

The total number of vacancies or positions are 1. Out of which for General/Un-Reserved/OC (Other Castes) vacancies are 0. For OBC (Other Backward Classes) total positions reserved are 0. For SC (Scheduled Castes) category job positions reserved are 0 and for ST (Scheduled Tribes) category job positions reserved are 0. For all other categories of reservations total positions alloted are .

The minimum and maximum age limits to apply for job consultant is minimum age limit is 0 and maximum age limit is 65.

The more and other important information related to this job specified as Period of contract – 11 months. Responsibilities: 1. To identify training requirements and guidelines regarding clinical trials implementation in India. 2. To develop policies and principles of good clinical practices (GCPs), including adequate human subject protection (HSP) as a critical requirement to the conduct of research involving human subjects. 3. To prepare documents on similar frames of the Food and Drug Administration’s (FDA’s) regulations for the conduct of clinical trials. 4. To undertake visits to institutions for proper monitoring of research grant, 5. To interact with the concerned officers of the institutes for the process of clinical trial

Important dates to be remembered related to this notification are as follows.
Date of Issue of Notificaition : . Applications will be issued from date and last date to submit applications is . The admit cards will be issued from to . The Priliminary Examinations will start from and will lasts upto date of . The Preliminary Examinations Results will be announced on date . The Main Examinations will start from date and will ends on . The answer keys for mains examinations will be announced on . The results for Main Examinations will be declared or announced on date . Job Interviews for this job positions consultant will be held from date and will ends on date . The final results or shortlisted persons for this job consultant will be announced on .

This notification issued by which is located in city and in state .

For More Details related to this Notificaition, for Complete Job Details and for complete Notificaition, Please visit the official website of organization .

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Job Organization / Department

• department of health research
• clinical trials training guidelines

Job Positions

• consultant

Job Educational Qualifications

• a person having m.d. /m.s.
• degree in medical subjects or 1st class master degree in life science

Job Eligibility Details

Job Experience Requirements

• minimum 10 years of experience.
• adequate experience in handling research projects and formulating policy/strategy documents

Job City, State

• delhi

Job Total Vacancies

• 1

Job Reservation Details

• General / Un-Reserved : 0
• OBC : 0
• SC : 0
• ST : 0
• Others :

Job Payscale / Salary

• Rs.80,000 - 1,00,000

Job Age Details

• Minimum Age : 0
• Maximum Age : 65

Job More Information

• period of contract – 11 months. responsibilities: 1.
• to identify training requirements and guidelines regarding clinical trials implementation in india. 2.
• to develop policies and principles of good clinical practices (gcps), including adequate human subject protection (hsp) as a critical requirement to the conduct of research involving human subjects. 3.
• to prepare documents on similar frames of the food and drug administration’s (fda’s) regulations for the conduct of clinical trials. 4.
• to undertake visits to institutions for proper monitoring of research grant, 5.
• to interact with the concerned officers of the institutes for the process of clinical trial

• Organization :
• Organization City, State :
• Organization Website :