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GCP Auditor

ClinForce

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Job Snapshot

Location:

Wilmington, DE ( map it!

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Employee Type:

Contractor

Industry:

Pharmaceutical
Biotechnology

Manages Others:

Job Type:

Biotech
Pharmaceutical
Research

Education:

4 Year Degree

Experience:

At least 3 year(s)

Travel:

None

Post Date:

10/30/2009

Contact Information

Phone:

800-964-2877

Ref ID:

CB1385

Fax:

866-941-1400 instantly fax your resume >>

Description ClinForce is currently seeking a GCP Auditor for Wilmington, DE.

Successful candidate will be responsible for the following:

Plan, conduct and report audits of Clinical Investigator Sites, Vendors, Clinical Study Reports, Clinical Databases, Trial Master Files, and High Level Clinical Documents (e.g., CTD).
Maintenance of appropriate GCP audit documentation.
Follow-up on audit findings and corrective actions to closure.
Assist with development and revisions of departmental SOPs.

Requirements 3-5 years experience in monitoring/clinical trial auditing in the Pharmaceutical or Biopharmaceutical industry required.
Minimum 3 years experience in a quality related function required.
Minimum 3 years performing GCP audits of clinical investigator sites.
BS/MS

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