Date Posted: 2019-05-25 | Date Modified: 2019-04-25 | Expires: 2019-06-24

GCP Technical Writer

Job Description

The resource should have a strong Clinical background to create the clinical SOPs for the client. Good writer. Good communicator. Will need to facilitate working and review sessions. Track progress and ensure deliverables are on time.

Partner with business area leaders and stakeholders to write/rewrite a complete set of GCP procedures

Work with leadership and a project coordinator to define a roadmap to deliver all procedures within the time allowed

Thorough knowledge of current good clinical practices (GCP) and the complete regulatory context

Good communicator

Technical writing (Clinical SOPs)

Requirements

The resource should have a strong Clinical background to create the clinical SOPs for the client. Good writer. Good communicator. Will need to facilitate working and review sessions. Track progress and ensure deliverables are on time.

Skills

Good Clinical Practice (GCP) Standard Operating Procedure (SOP)

Language Requirements

English

Visa Support

No

Accepting only candidates from:

United States
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Job Criteria

Job Type

Contract

Industries

#Medical Devices #Pharmaceuticals

Job Location

United States - Lexington

Functions

Writing/Editing

Salary

Negotiable

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