Jubilant Pharma Limited is a global integrated pharmaceutical company offering a wide range of products and services to its customers across geographies. We organise our business into two segments, namely, Specialty Pharmaceuticals, comprising Radiopharmaceuticals (including Radio pharmacies),Contract Manufacturing of Sterile Injectable, Non-sterile & Allergy Therapy Products, and Generics & APIs, comprising Solid Dosage Formulations & Active Pharmaceutical Ingredients.
All BA/BE studies are done In house at our 80 Bed facility which is inspected and having approvals /certifications from
The Drugs Controller General (India) and has global regulatory accreditations including USFDA, EMEA, ANVISA (Brazil),INFRAMED (Portugal Authority),NPRA(Malaysia),AGES MEA (Austria) for GCP and NABL, CAP accreditations for Path lab services. JGLs full-fledged Regulatory Affairs & IPR professionals ensures unique portfolio of patents and product filings in regulatory and non-regulatory market.
Designation- Research Associate- Clinical Research BA/BE
Qualification- M. Pharmacy Experience- 2-4 Yrs Protocols submission to Ethics committee.
Coordination with the EC members and arrangement of EC meeting for the protocol approval. Submitting of protocols for the IEC meeting submission copy as well as the member copy. Submitting the all types of related documents to the ethics committee for their approval. Maintaining the documentation records for the Regulatory Authoritarian. Preparation of compensation of volunteers. Submission of protocol to the DCGI. Monitor applicable regulatory requirements; assure compliance with the companys and external standards preparing the all DCGI documents after the Ethics approval which is required to the DCGI approval