Ensure submission and approval of high-quality regulatory applications within planned timelines and Facilitate interactions with regulatory bodies on a regular basis for approvals.
Assist in management of Biotechnology laboratories. Maintain and coordinate use of scientific equipment and infrastructure. Preparation of scientific reports. Maintenance of data-bases. Preparation of technology related policies, IPR and legal issues. Perform any other duties assigned to him, her by the Executive Director from time to time.
Project Research Scientist conducts monitoring visits for assigned trial protocol and trial sites. Overall responsibilities are to ensure that the trial is being conducted in accordance with the protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements.
Masters degree in any branch of Life Sciences from a recognized University with four years post qualification research experience. OR Ph.D. in Life Sciences from a recognized University. Candidates who have submitted Ph.D. thesis may also apply for this position
Women researchers who have completed Ph.D. in any discipline of Biotechnology, Life Sciences or allied areas, interdisciplinary sciences, MD, MDS, M.V.Sc.
Post-Graduate degree in any branch of life sciences from a recognized University with atleast three years of post- qualification research experience in the field of biochemical and molecular biology.
Post-graduate Masters degree in Life Sciences, Chemistry with minimum 60% marks or PhD in Life Sciences, Chemistry. Should have a minimum of three years post qualifying with Masters degree of hands on experience and demonstrated productivity in one
PhD in any branch of Life Sciences from a recognized university or equivalent with a minimum of three years of post- qualification research experience in the relevant field. At least one publication as first author in a scientific journal.
Ph.D. in clinical sciences, life sciences, pharmacy, public health, healthcare, or other related disciplines with at least 2 years of work experience in Clinical Project Management and, or Clinical trial, Study monitoring