Hyderabad

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.

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

Support DRL sponsored or investigator initiated studies, real-world evidence generation, and post-marketing surveillance, as and when required

Cohance Lifesciences is not just a brand it’s a culmination of vision, scientific ambition, and purposeful integration.

Bachelor of Science in a science-related field such as Pharmacy, Chemistry, Biological Sciences or related Life Sciences.

Bachelors degree required advanced degree preferred, scientific discipline preferred with at least 2 years of operational experience in pharmaceutical production, Supply Chain, Quality and/or clinical trials.

Team spirit and cross-functional collaboration. Excellent analytical skills and learning agility; able to quickly grasp new concepts and absorb large amounts of information under pressure.