Cadila Pharmaceuticals Ltd - Walk-In Drive for Multiple Positions on 22nd December 2018

Dear Candidate,
Greetings of the day!! 
Cadila Pharmaceuticals Ltd. is conducting a Walk-In Drive to fulfill the technical requirements at Plant based at Dholka (Gujarat).
Walk-In Detail for 22.12.18 (Saturday) at Dholka Location. 

·         Address : Survey No 1389, Trasad Road, Dholka, Gujarat 382225

·         Time : 9 AM to 4 PM

·         Contact : Plant HR

Position Details :  

·         Clinical Data Management:- M.Pharm / M.Sc / Computer science graduate with 2 to 5 yrs working experience in Clinical data management, Query resolution, Discrepancy Management in EDC, Paper based studies , Preparing of data entry guidelines, self Evident correction convention (SECC), final QC report, DMP (Data Management Plan).

·         Biostatistician:- M.sc (Stat) / M. Pharm (with certificate course of biostatistics) having 2 to 5 yrs of experience in Providing Statistical inputs to BE protocol, Clinical trial Design, Sample size calculation. Generation of Randomization schedule, tables and listing. Responsible for Pharmacokinetic and statistical analysis for BA/BE, clinical trials and pre-clinical studies. 

·         Data Programmer:- M.Pharm / M.Sc / Post graduate in computer science with 2 to 5 years working experience in Preparation of data management plan, Preparation of annotated CRF, Database design, Edit Check programming. Preparation data validation documents for EDC and paper based studies, Generate data extract views. Perform critical and final data QC activities.

·         Doctor :- MBBS / MD, Experience with 2 to 4 years. Responsible for adherence to ICH GCP and conduct of the studies as per ICMR guidelines for ethical conduct of biomedical research involving human subjects. To work as clinical/ principal investigator for BA/BE, clinical trials and PK studies. 

·         Study Coordinator:- M.Pharma / M.sc, Experience:- 1 to 4 years. Reviewing of protocol and informed consent from for BA/BE study. Managing and submission of study documents to independent ethics committee(IEC). Registration and screening of the volunteers. Monitoring BE study. Review of Clinical study report. Also to work as deputy pharmacist.

·         CRA:- M.Pharma / M.sc with 2 to 6 years of experience Co ordinate to sites for IEC regarding study related required approval and notifications. Charting of site initiation, monitoring plan. Drafting of budget and plan for whole projects in tentative amount of laboratories, sites, printing of documents, submissions etc. Periodic monitoring to various sites. Co ordinate with the ethics committees.

·         QA:- M.Pharma / M.sc, Experience:- 2 to 6 years. Experience of Issuing controlled / documents, and approved uncontrolled / usage copies of SOPs, forms / formats / logbooks, study documents of CRO. Issuing controlled / documents, and approved uncontrolled / usage copies of SOPs, forms / formats / logbooks, study documents of CRO.