M.Pharm

Assist in the preparation of response packages to Health Canada requests in a timely manner to minimize delays in the submission review process. 

Designs and coordinates the overall direction of clinical development projects. Coordinates activities of associates and investigators to ensure compliance with protocol and overall pre-clinical objectives. Maintains a high level of professional expertise through familiarity with clinical literature and participates in project team meetings

B. Pharmacy/D.Pharmacy/ Pharma-D/M.Pharmacy course after intermediate recognized by the Govt, of A.P.  Any other eligible equivalent Qualification must be registered With AP Pharmacy council with Updated renewal. 

B.Pharm / M.Pharm ; Preference will be given to candidates who have experience working in clinical trials.

Ph.D in Bioengineering, Biomedical engineering, Mechanical Engineering with First class or equivalent grade at the preceding degree M.Sc, M.Pharm, M.S.Pharm, B.Tech, M. Tech in relevant field with a very good academic record.

Support business partners in assessing brief submitted by project sponsors for each new project. Identify any gaps and missing information to be collected with the sponsor.

M.Pharm with 3 years of post PG experience in research/projects and at least one research paper in SCIE journal

M.Tech / M.S (Pharm) / M. Pharm / MSc in Pharmacy / Nanotechnology from a recognized University with sound knowledge in the application of nano formulations in drug delivery plus GPAT/GATE/NET/ any national- level entrance test, qualified

Preparation and characterization of Phytopharmaceutical, in-vitro and in-vivo behavioral and neuropathic pain models, network pharmacology.