Freelance Clinical Research Associate
- Company
- RBW Consulting
- Location
- Poland
- Salary
- On application
- Posted
- 23 Feb 2021
- Closes
- 25 Mar 2021
- Discipline
- Clinical Research
- Hours
- Full Time
- Contract Type
- Contract
- Experience Level
- Entry level
I am partnered with a small, niche CRO which is looking for a Freelance Clinical Research Associate based in Poland for 1 FTE over a 6 or 12 month contract.
Responsibilities:
- Perform on-site monitoring visits as well as site identification, feasibility and selection as required
- Assist in the preparation and management of regulatory and ethics applications for clinical research studies as required
- Prepare project-specific support materials and templates in accordance with protocol and other specifications
- Manage the content of project site-level Trial Master Files and ensure accuracy and completeness
Requirements:
- Background in multiple therapeutic areas
- Driving Licence with ability to travel to sites when needed
- Fluent in Polish and English
- Independent monitoring experience of a minimum of 2 years needed
- Experience with regulatory and ethics submissions across clinical trials
If you’re interested in this role, please get in touch and I will be happy to discuss this in further detail: Roxanna.keshavarz@rbwconsulting.com or +44 1273 952187
Apply for Freelance Clinical Research Associate
Already uploaded your CV? Sign in to apply instantly