Job description

Requirements

  • Entry level
  • No Education
  • Salary to negotiate
  • INDIA, IN

Description

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QA AUDITORS-Part Time / Project Basis – All Major Cities

CRQA – www.crqa.in is an upcoming clinical regulatory quality assurance firm, established by the senior professionals from the clinical research and pharmaceutical industry.

CRQA is looking for QA and Auditing professionals on part time or assignment basis at various locations in India with auditing experience in the following areas

GCP Audits

Clinical Operations

CRO Audits

Central Lab and Bio analytical Lab Audits

Clinical Trial Supply Audits

IRB Audits

System Audits

Data Management Audits

Essential Document Audits

Pharmacovigilance Audits

GLP / GMP Audits

SOP Development

Regulatory Inspections Preparations

KEY RESPONSIBILITIES

Perform QA audits of clinical trial data and records in order to assure compliance with client SOPs, study protocols, GCP guidelines, relevant regulations and ISO 9000 requirements.

Plan and conduct regular and random QA audits.

Perform quality system audits and contract audits for Sponsors.

Ensure that audit results are formally recorded and reported and that corrective/preventive actions are documented.

As an auditor, perform the duties assigned in an efficient and effective manner. This includes liaison with the sponsors on all QA issues, including audit planning and review of audit results.

QA Training.

QUALIFICATION & EXPERIENCE

Qualification in medicine, science and/or other relevant discipline and appropriate experience.

Previous experience in Quality Assurance auditing – 2 – 5 years.

Detailed knowledge of GCP guidelines and relevant regulations for the conduct of clinical trials.

Ability to review and evaluate clinical data / records.

Excellent communication and interpersonal skills.

These are part time / project assignment based positions. Only apply if you are interested in working on part time / project basis. Kindly apply in confidence with your detailed CV detailing your QA / Audit experience to bd@crqa.in – www.crqa.in.

What's New

CRQA is looking for

qualified and Independent

Pharmacvovigilance Auditor


- experience essential in

Pharmacovigilance Audits.

Interested Professionals

may apply to bd@crqa.in

CRQA is looking for

qualified and Independent

Pharmacvovigilance Auditor


- experience essential in

Pharmacovigilance Audits.

Interested Professionals

may apply to bd@crqa.in


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