QA Specialist/ SOP Writer- CRO

By: Pharma Jobs | Views: 2548 | Date: 24-May-2011

Tech Observer is a client-centric global Clinical Research Organization (CRO) providing innovative solutions and analytical support for all clinical research needs. We works closely with global Pharmaceutical and Biotechnology companies worldwide.

TECH OBSERVER

Summary
 

Experience:

1 - 3 Years

Location:

Delhi

Compensation:

Negotiable

Education:

UG - Any Graduate - Any Specialization PG - Any PG Course - Any Specialization

Industry Type:

Pharma/ Biotech/Clinical Research

Role:

Documentation/Medical Writing

Functional Area:

Healthcare, Medical, R&D

Posted Date:

24 May

Desired Candidate Profile

Documents audit observations; evaluates impact, and makes recommendations for corrective actions.

Bachelor’s degree with 1-3 years relevant experience in CRO industry;

Excellent documentation skills.

Job Description

Write & Manage & Compose SOPs for DM, Biostats and Clinical Research as per 21CFRPart11

Create and Modify existing Quality Systems

Serves as clinical QA representative on clinical project teams, conducts internal and external CQA audits

Keywords: QA, Quality Systems, SOPs, CRO, Clinical Writer

Company Profile

Tech Observer is a client-centric global Clinical Research Organization (CRO) providing innovative solutions and analytical support for all clinical research needs. We works closely with global Pharmaceutical and Biotechnology companies worldwide.
Contact Details
Company Name:

TECH OBSERVER

Address:

Not Mentioned

Email Address:

hire@tech-observer.com

Telephone:

Not Mentioned

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