Covance is one of the world’s largest and most comprehensive drug development services companies with more than 11,000 employees in 60 countries. Through its nonclinical, clinical and commercialization services, Covance has helped pharmaceutical and biotech companies develop one-third of all prescription medicines in the market today.
Post : Clinical Trials Administrator I
Job Description
• Assist in preparation of Clinical Trial Application (CTA) dossier(s) to be submitted to the Health Authority (HA), along with the other administrative aspects (e.g. maintaining files, trackers, coordinating with the monitoring team, scanning and uploading documents in eTMF appropriately in a timely manner ).
• Assist in preparation and submission of any queries / amendments to HA, as well to notify about the other study updates (e.g. start- end of studies, any DMC recommendations, updated Investigator undertakings, ).
• Participate / follow-up in Regulatory meetings with Health authorities at local level
• Collaborate with the affiliate regulatory team in order to follow-up on all submitted CTAs and obtain its
• Manage and update the database that includes information related to all CSU trials.
• Assist in registration of the clinical trials on the CTRI
• Acts as a back-up, in absence of CTARM.
Candidate profile
• Bachelor of Science degree preferred or an equivalent scientific or commercial education with preferably experience in the healthcare field, pharmaceutical industry or clinical research.
• Minimum one (I) year administrative experience or equivalent training. Good oral and written communication skills.
Additional Information
Experience : 1 years
Qualification : B.Sc
Location : Delhi
Industry Type : Pharma / Healthcare / Clinical research
End Date : 25th April, 2020
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