M.Pharm

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.

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.

Alkem Laboratories Limited established in 1973, is amongst the top five leading Indian Pharmaceutical Companies with global operations.

I.T.I, Diploma, B.Sc.,With Relevant Experience in Production B. Pharm, M.Sc, M.Pharm with relevant experience in QC.

Exercising excellent interpersonal communication skills to effectively and professionally liaise with the internal teams, healthcare professionals, and other key stakeholders

Masters Degree in Sciences or related field with 3-5 years exp in Pharmaceutical / Biotechnology / Clinical research

Professionals having proven competency and success in their area of specialization, with at least 10 years of post- qualification experience and should possess minimum M.Sc / B.Tech / BE /МСА / MPH / B.Pharm / BAMS / BSMS / MD in AYUSH or equivalent qualifications in relevant subject.

Candidates having M.Sc. / M. Tech / M. Pharm. / M.V.Sc. or equivalent qualification in Life Sciences or allied subjects Botany /Zoology /Biochemistry / Biotechnology / Virology / Bioinformatics / Computational Biology / Microbiology, etc.