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Opportunity to open for DM QC Specialist @ inVentiv Health


Clinical courses


Clinical research courses

inVentiv Health Clinical, a leader in drug development services, has a global infrastructure, therapeutic expertise, and commitment to quality that is unmatched in the industry. For pharmaceutical, biotechnology, generic drug, and medical device companies of all sizes around the world, inVentiv Health Clinical can help you transform promising ideas into commercial reality.

Post: DM QC Specialist

Job Description:

  • Perform QC of the following:
  • Study-specific documentation, e.g., Data Management Plans, Guidelines,
  • approval forms
  • Database design and associated set-up activities
  • Data entry and verification
  • Laboratory normal ranges
  • Data validation
  • Perform rolling, interim and final QC Inspections of the Clinical Study Database
  • Coordinate the work of Quality Control Associates I for assigned projects
  • Train QC and additional DM personnel on project-specific QC requirements
  • Coordinate QC activities conducted by others in the department
  • Prepare documentation of QC findings
  • Assist in preparation for sponsor or regulatory audits
  • May participate in corrective action plans
  • May assist in performing QC of Computer System Validation (CSV) documentation
  • Assist in collecting and maintaining project metrics

Candidate Profile:
•1+years of experience in DM activities
•Preferred to have candidates with Q.C knowledge.
•Candidates with 2 years of Pharma experience will be considered
•Clinical Research diploma freshers with D.M knowledge are also eligible.
•Should possess good communication skills

Additional Information:
Experience: 1-2 Years

Industry Type: Clinical Research
Functional Area: QC
Last Date: 24th Nov, 2013


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