CRA / cardio
WarszawaWarszawa
NR REF.: 1019647
Clinical Research Associate /cardio
My client, one of the biggest CROs in Poland which carries out clinical research in Central & Western Europe is currently looking for an office-based Clinical Research Associate in Warsaw.
ONLY EXPERIENCED CANDIDATES WILL BE CONSIDERED
Summary of Job Specification:
Conducts site monitoring of clinical research studies according to Standard Operating Procedures and GCP Guidelines
Travel Required:
Available for travel from 50% to 80% of the time, including overnight stays as necessary, consistent with project needs and office location
Ability to drive and have a valid driver’s license
Education / Qualifications Required:
University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology)
Knowledge of GCP, monitoring procedures, basic understanding of regulatory requirements
Experience / Skills Required:
Minimum of two (2) years of clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits)
Ability to monitor study sites independently according to protocol monitoring guidelines, SOP, GCP
Good planning, organization and problem solving abilities
Job Description
Warszawa
NR REF.: 1019647
Clinical Research Associate /cardio
My client, one of the biggest CROs in Poland which carries out clinical research in Central & Western Europe is currently looking for an office-based Clinical Research Associate in Warsaw.
ONLY EXPERIENCED CANDIDATES WILL BE CONSIDERED
Summary of Job Specification:
Conducts site monitoring of clinical research studies according to Standard Operating Procedures and GCP Guidelines
Travel Required:
Available for travel from 50% to 80% of the time, including overnight stays as necessary, consistent with project needs and office location
Ability to drive and have a valid driver’s license
Education / Qualifications Required:
University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology)
Knowledge of GCP, monitoring procedures, basic understanding of regulatory requirements
Experience / Skills Required:
Minimum of two (2) years of clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits)
Ability to monitor study sites independently according to protocol monitoring guidelines, SOP, GCP
Good planning, organization and problem solving abilities
Additional Information
- Last updated
- Employment type
- Full time
- Contract type
- Permanent
- Number of vacancies
- 1
- Min. experience
- One year
- Min. education
- Associate degree
- Industry / category
- Jobs in Laboratory / Pharmacy / Biotech