Candidate with Diploma / B.Sc in Pharmacy. Candidate should have passed Intermediate / 10+2 / Equivalent Examination with Physics, Chemistry, Biology and English
ECHS invites application to engage following Medical, Para Medical & Non Para Med Staff on contractual basis in respect of ECHS Polyclinic Bareilly, Badaun, Rampur & Moradabad under ECHS Cell Bareilly. BPharma and approved DPharma
Post Graduate degree in basic science or Graduate / Post Graduate Degree in Professional Course selected through a process described through National Level examinations conducted by CentraI Government Departments and their Agencies and institutions such as DST, DBT, DAE, DOs, DRDO, MHRD, ICAR, ICMR, IISc, IISCR etc
Indian Council of Medical Research (ICMR) provides financial assistance to Indian scientists working outside ICMR institutes to conduct research in the fields of medicine, public health, and allied disciplines aimed at improving the health of Indians under its Extramural Research Programme.
M.Sc/ B.Pharm / M.Pharm. To plan, prepare and review of high quality dossier with support and guidance, assuring technical concurrency and regulatory compliance, meeting agreed upon timeline.
Doctor of Philosophy (Ph. D) Degree in the relevant field from a recognized University / Institution and first class or equivalent at either Bachelors or Masters level in the relevant branch.
1st class Masters degree in Life Sciences from a recognized University with 2 years experience in the related field or 2nd class Masters Degree with Ph.D in relevant subject from a recognized University.
Postgraduate in Genetics & Plant Breeding/Plant Pathology/Agricultural Botany/Plant Biotechnology/ or any other branch of Life Science with at least 55% marks. Candidates who have qualified National Eligibility Tests ICAR, CSIR, UGC-NET and GATE
Applicants must be nationals of Djibouti, Ethiopia, Kenya or Uganda in order to apply. Displaced researchers currently working in any of the four countries are considered nationals of these countries.
The overall objectives of the BIO-GRID network should be to create a robust ecosystem where bioinformatics serves as the catalyst for transformative discoveries, bridging the gap between data
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
Works in close collaboration with the external service provider and Investigators to ensure quality and quantity commitments are achieved in a timely and efficient manner.
Managing initial clinical trial application submissions in the EU according to the Clinical Trial Regulation and all changes during the life cycle of clinical trials.