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Hays Poland

CRA / cardio

Warszawa, mazowieckie Full time

Hays Poland

CRA / cardio

Warszawa
CRA / cardio
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
Prosimy o aplikowanie poprzez przycisk znajdujący się po prawej stronie ogłoszenia.
Hays Poland

Job Description

CRA / cardio
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