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Clinical Data Associate I/II @ InVentiv

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 Clinical Data Associate I/II

Desired Candidate Profile


Roles and responsibilities 

The position is responsible for assisting in carrying out basic clinical data management activities required for clinical trials .

.Assist in basic database and edit check testing activities.

.Perform data review and query generation.

.Update the database to correct errors.

.Assist in the completion of all activities necessary for the finalization and
transfer the clinical database and related project documents to the sponsor.

.May be required to participate in client, internal or agency audits and inspections

.Responsible for performing activities that are in compliance with applicable
.Corporate and Divisional Policies, Standard Operating Procedures and
.Operating Guidelines and performing other duties as assigned by
management.


Note: This job description describes the principal and main elements of the job. It is a guide to the nature and main duties of the job as they currently exist, but is not intended as a wholly comprehensive or permanent representation.

Required Candidate profile

  • Minimum 2 years of experience in CDM (Clinical Data Management)
  • Minimum 2-4 years of experience in Lab Data Management
  • Good Communication Skills

Education:

UG:   Graduation Not Required,

PG:  Post Graduation Not Required,

Doctorate:  Any Doctorate - Any Specialization,

Contact Details:

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Keyskills:   clinical data management query management

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InVentiv

inVentiv International Pharma Services Pvt. Ltd. Join an industry-changing company that is reinventing the way we develop and commercialize drugs. At INC Research/inVentiv Health our 22,000 employees have one purpose: shortening the distance from lab to life. You will work alongside the bright...