GCP SOP Development for mid-size Pharma Client
See more projectsIntensity
20hr/week
Est. Duration
6weeks
Work Remotely
Work from your own location. No travel is required to apply to this project.
Schedule Expectations
Expert can manage their own schedule
Communication Expectations
(None Provided)
Project Overview
8 to 15 years professional experience
Operations - Compliance and risk
Our firm is a life science focused consulting firm that supports biopharma clients from strategy development through implementation.
We are engaging with a mid-size pharma company looking to do an assessment of the R&D SOPs and other procedural documents to identify any gaps in regulations as well as any critical misses they have in their documentation. In particular, we would want a candidate who has GCP documentation (i.e. SOP) experience.
This project would range between 20-30 hours a week and last through the end of the year.
We are engaging with a mid-size pharma company looking to do an assessment of the R&D SOPs and other procedural documents to identify any gaps in regulations as well as any critical misses they have in their documentation. In particular, we would want a candidate who has GCP documentation (i.e. SOP) experience.
This project would range between 20-30 hours a week and last through the end of the year.
Additional Notes
Must have extensive SOP/GCP experience Preferred Background
Sector Experience
Life Sciences & Pharma
Preferred Skills and Certifications
Functional
Compliance and risk
About The Client
Top Skills Hiring For
Project Management
Compliance and risk
Program Management
Business Analysis
Clinical Development
$3.1M
Total Spent
8 years
Time On Graphite
10
Hiring Managers