vacancies

B.Pharm / M. Pharm with experience in R&D or a related role. Strong Analytical, Problem-solving, and Critical thinking skills., Excellent Communication and Coordination skills.

Regualtory Specialist II supports a team in the preparation and maintenance of complete and accurate regulatory documents in support of clinical research studies

Principal Clinical Data Standards Specialist is responsible for the development, maintenance and implementation of Industry CDISC and regulatory compliant Clinical Data Standards, providing expert support to business users and teams on their use in line with the Clinical Data Standards strategy.

Professionals having proven competency and success in conducting Quality Assurance and / or managing studies under GLP (Good Laboratory Practice environment, with at least 10 years of post- qualification experience, and should possess M.Sc./ M.V.Sc. / M.Pharm / M. Tech qualification.

Diploma in Pharmacy OR Bachelor Degree in Pharmacy (B. Pharm) from a recognized institution and registered as Pharmacist under the Pharmacy act 1948

M.Sc. degree in Zoology / Biochemistry / Biotechnology / Life Science with first class in graduation and post-graduation. 

Post Graduation in Science M.Pharm, Life Sciences, Biotech, Zoology, Botany, etc. PG Diploma in Clinical Research is mandatory with one year experience is desirable.

Post-Graduate degree in any branch of Life Sciences, including the integrated PG degree, from the recognized university.

Ph.D. holder full-time Ph.D. project shall be related to Clinical Embryology or assisted reproductive technology or fertility from a recognised university with an additional one year of human ART laboratory experience.