Docs Global (Continental Europe)

Clinical Research Associate I / Clinical Research Associate II

Warsaw area, Poland
23 Apr 2021
23 May 2021
Full Time
Contract Type
Experience Level
Experienced (non-manager)
The Clinical Research Associate (CRA) acts as a liaison between site staff and Pharmaceutical Company, working within Polish Affiliate supporting one or more clinical trial(s) in a development programme. CRA is responsible for clinical trial operational targets (KPIs) and ensuring the highest possible data quality in clinical trial(s).

You will work home- or office-based (Warsaw area only) and report to Clinical Team Manager, Poland and will require travelling up to 60% of the time.

- The primary point of contact between site staff and Client
- Leadership of site management for the selection and initiation of sites as well as conduct and closing activities of the appointed studies in compliance with local regulations, ICH-GCP, Client procedures and protocol requirements to ensure data quality and study subject protection
- Managing the site to meet patient recruitment rate and target
- Delivery of results that have direct impact on the successful completion of the clinical programme
- Communication about progress and critical issues that may impair trial progress to Trial Manager (TM)

What is required:
- Experience as CRA in the pharmaceutical industry or CRO, preferably with a minimum of 1 year of independent on-site monitoring experience is a must
- Ability to build and maintain relationships with sites
- Excellent communication and negotiation skills
- Adequate English verbal and writing skills, e.g. enabling understanding of the protocol and study documents as well as writing monitoring reports
- Ability to manage multiple priorities
- Team oriented personality with high degree of flexibility

To Apply:
Please contact Dagmara Drozdowska Recruitment Consultant at DOCS , email your up-to-date CV to:

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