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

Bachelors degree in life sciences, pharmacy, or a related field. An advanced degree is preferred. Extensive experience in pharmacovigilance or drug safety reporting, with a strong understanding of relevant regulations and guidelines.

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.

B.Pharma or Bachelors degree in Engineering or Technology or Medicine or from a recognized University of equivalent. 

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.

Liaison Officer will maintain database of all projects, update project changes, act as link between the SRC and the project personnel to facilitate smooth function of ISRC-I & II, NIEC l & ll meetings.

First Class Post Graduate Degree in relevant subjects Public Health, Life Sciences, Biostatistics, Epidemiology, Biotechnology.

Applicants having postgraduate degree and holding a valid Junior Research Fellowship from CSIR, UGC, DBT, ICMR, BINC can apply.

Post Graduate Degree in Life Sciences/ Post Graduate degree in the professional course selected through a process described through National Eligibility Test- CSIR-UGC NET including lectureship and GATE.

1st class Post Graduate Degree, Including the integrated PG Degree in Life Sciences Or 2nd Class Post Graduate Degree, Including the integrated PG Degree with PhD in Life Sciences

BS degree in Pharmacy or Life Sciences or relevant education. Minimum 1 year of relevant experience in regulatory affairs, quality or product development in the pharmaceutical, medical devices or similar FMCG industries.

Identify and execute appropriate workup and purification technique to produce an intermediary / final compound of desired quality

The objective of the role is to perform chemical synthesis of molecules, the role involves process development, process validation and transfer to production units.

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.