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  • Applicants Less than 5 Applicants
  • 2017-09-17

Job Description

Hiring Life Science Graduates with experience and TRAINED in CRA/CRO/CDM/PV/Regulatory

Any Life Science graduate with an exposure to Clinical research domain

Having a prior exposure/experience in Clinical document management/ Clinical data management/ Clinical research co coordinator /Clinical research associate

Medical coding / QA QC in clinical research / Regulatory affairs/ Regulatory publishing / PV

Any intern in clinical research and clinical data management with 3 months of experience

Knowledge of ICH GCP principles and Clinical drug development process

Minimum 3 months to 1 year of experience in the clinical research field

Location : Hyderabad/ Chennai/Pune Locations

Job Type: Full-time


IT-Hardware & Networking / IT-Software / Software Services

Functional Area

IT Software - Others

Number of Vacancy



B.Pharma, B.Sc, MBBS, MS/Master of Surgery, M.Pharma, M.Sc, Any Doctorate Degree

About Ancla Consultancy services India pvt Ltd

Ancla is a global IT and knowledge based service provider for the Pharmaceutical and Biopharmaceutical industry. We partner with you through the entire drug development cycle, to provide a full range of services from study design to post marketing services. Our expertise lies in helping you stream line your drug safety operations to consistently regulatory compliance and standards. Our processes leverage technology and capability of our people to deliver efficiency.

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