Clinical Research Trainer

Key Skills

Handling Technical Assets Laptop Ms Office Outlook IWRS RMP ECRF

Job Description

Expert knowledge of ICH-GCP, Schedule Y and applicable regulatory requirements

Delivering lectures for Clinical Operations, Medical Writing, Clinical Data

Management, Pharmacovigilance and any other Clinical Research topic that may be

assigned.

Scheduling, planning and coordinating of lectures, exams, results for PT / FT / Distance

/ Online for CR and Regulatory Affairs courses

Ensure smooth completion of all batches and program structure of each course is

followed completely.

Placement tie ups with appropriate companies, generating placements to all CR & RA

students. Developing strong placement file.

Required Education:

Life Science Graduate PG / Masters in Clinical Research.

Required Experience:

2 to 3 yrs of Clinical Research Experience
  • Experience2 - 3 Years
  • No. of Openings1
  • EducationAdvanced/Higher Diploma, B.Pharma, Post Graduate Diploma, M.B.A/PGDM, M.Pharma
  • RoleClinical Research Trainer
  • Industry TypeHospitals / Medical / Healthcare Equipments
  • Gender[ Male / Female ]
  • Job CountryIndia
  • Job TypeWork from Office

About Prorelix Education

ProRelix Research (ProRelix Services LLP) is offering several professional services and resources for drug development and analysis on the industry to support clinical research. We specialize in a wide range of tools and resources to aid patient and investigator recruitment, remain current with industry trends and business practices, and strengthen organizational procedures. Our strong database and a fine assortment of industry resources make us an adept organization. In a highly fragmented industry, we are one of a group of organizations with the capability and expertise to conduct clinical research. We have the operational flexibility to provide drug development services on a stand-alone basis or as part of an integrated full service solution.
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