M.Pharm, MSc Job in multiple departments at Cadila Pharmaceuticals Ltd | Virtual Interview

Cadila Pharmaceuticals Ltd. is one of the largest privately-held pharmaceutical companies in India. Over the past six decades, we have been developing and manufacturing affordable medicines for patients around the world. Our innovation-led drug discovery processes ensure the health and well-being of people around the world. Our enhanced investment in innovation and a strong track record in research and development have produced medical miracles that have changed lives and made a profound impact on real life.

Clinical Data Management
Qualification : M.Pharm/M.Sc/Computer science graduate
Experience : 2 to 5 yrs
Job Description
• 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
Qualification : MSc (Stat )/ M. Pharm (with certificate course of biostatistics)
Experience : 2 to 5 yrs
Job Description
• Providing statistical inputs to BE protocol
• Clinical trial design
• Sample size calculation
• Generation of randomization schedule, tables and listing
• Pharmacokinetic and statistical analysis for BA/BE, clinical trials and pre-clinical studies

Data Programmer
Qualification : M.Pharm/M.Sc/Post graduate in computer science
Experience : 2 to 5 yrs
Job Description
• Preparation of data management plan
• Preparation of annotated CRF
• Database design and edit check programming
• Preparation of data validation documents for EDC and paper based studies
• Generate data extract views
• Perform critical and final data QC activities

Study Coordinator
Qualification : M.Pharma /M.sc
Experience : 1 to 4 years
Job Description
• Reviewing of protocoland informed consent for BA/BE study
• Managing and submission of study documents to independent ethics committee (I EC)
• Registration and screening of the volunteers
• Monitoring BE study
• Review of clinical study report
• Also to work as deputy pharmacist

CRA
Qualification : M.Pharma /M.sc
Experience : 2 to 6 years
Job Description
• Coordinate 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
• Coordinate with the ethics committees (USFDA trial experience preferable)

VIRTUAL WALKIN INTERVIEW
Date : 20 December, 2020
Time: 10.00 AM To 4.00 PM