January 2025

He, She will be expected to participate in project planning, recording and interpretation, evaluation of data, and communication of results. He, She will also be expected to acquire technical, lab management, and manuscript, grant writing skills; and participate in seminars, lectures, poster sessions and presentations at national meetings.

Pharmacology, Pharmacy Practice, Pharmaceutics, Biotechnology, Pharmacognosy, Pharmceutical Chemistry, Analysis. Norms as per the Pharmacy Council of India & The Tamil nadu Dr. MGR Medical University, Chennai.

Develop study protocols, standard operating procedures, and other essential documents in line with regulatory guidelines. Oversee the implementation of study activities, ensuring adherence to timelines, quality standards, and Good Clinical Practice guidelines. 

M.Pharm, B.Pharm, Diploma in Pharmacy with Kerala Pharmacy Registration.

B.Sc, MSc in Life Science, Pharma, Nursing, Master of Public Health MPH Should have adequate experience with clinical research projects. Proficiency in Hindi, English and Odia language. Proficiency in MS Word, Excel, Power Point & statistical Software.

M.Sc, M.S, M.Pharm in Chemistry, Organic Chemistry, Natural Products Chemistry from a recognized university or equivalent. Research experience, knowledge in Organic Synthesis, Natural Products Chemistry will be preferred.

Validating PIWIL mRNAs and their protein signatures as a predictive marker for fertilizing competence of the sperm in assisted reproductive technology- a multicentric cohort study.

To assist Director in all Academic, R&D, intellectual property & technology related matters, and faculty related activities of the institute. Proven track record of contribution to higher education, research projects and publications. Candidate must have strong research communication skill with analytical thinking. Past record of serving as administrative head/ intellectual property related work will be of added benefit. 

Preparation of SOPs, BMRs, Protocols, Interim and Summary Reports for products, and Qualification, Re-qualification documents.