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Hays Poland

CRA / cardio

Warszawa, mazowieckie Pełny etat

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

Opis stanowiska

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

Dodatkowe informacje

Ostatnia aktualizacja
Wymiar etatu
Pełny etat
Rodzaj umowy
Na czas nieokreślony
Liczba wakatów
1
Min. doświadczenie
1 rok
Min. wykształcenie
Policealne
Branża / kategoria
Praca Laboratorium / Farmacja / Biotechnologia