Dane pracodawcy
HAYS Poland
ul. Złota 59
00-803 Warszawa
tel. 48 22 584 5650
fax: 48 22 584 5651
e-mail:
strona WWW: http://hays.pl
więcej
ul. Złota 59
00-803 Warszawa
tel. 48 22 584 5650
fax: 48 22 584 5651
e-mail:
strona WWW: http://hays.pl
więcej
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Ogłoszenie z dnia 2012-01-28
HAYS Poland
HAYS Poland jest firmą doradztwa personalnego, należącą do międzynarodowej, notowanej na giełdzie w Londynie, grupy HAYS plc i największej na świecie firmy zajmującej się rekrutacją specjalistyczną.
Opis:
APLIKUJ TERAZ Dane pracodawcy:
HAYS PolandHAYS Poland jest firmą doradztwa personalnego, należącą do międzynarodowej, notowanej na giełdzie w Londynie, grupy HAYS plc i największej na świecie firmy zajmującej się rekrutacją specjalistyczną.
CRA /oncology
mazowieckie WarszawaOpis:
My client is a big R&D company which carries out clinical research in Central Europe. The company's clients include global pharmaceutical companies which outsource clinical research to contract research organizations.
Currently they are looking for experienced candidates for the position of:
Clinical Research Associate /oncology – Warsaw
CRA – office-based
Summary of Job Specification:
Conducts site monitoring of clinical research studies according to Standard Operating Procedures and GCP Guidelines
Job Duties and Responsibilities:
Responsible for all aspects of study site monitoring including: routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaising with vendors;
Conducts feasibility work;
Monitors Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs;
Independently performs CRF review; query generation and resolution against data review 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 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, S.O.P.s, GCP;
Good planning, organization and problem solving abilities;
Ability to work with minimal supervision;
Good communication and interpersonal skills;
Good analytical and negotiation skills;
Computer competency;
Fluent in local office language and in English, both written and verbal;
Inne: Currently they are looking for experienced candidates for the position of:
Clinical Research Associate /oncology – Warsaw
CRA – office-based
Summary of Job Specification:
Conducts site monitoring of clinical research studies according to Standard Operating Procedures and GCP Guidelines
Job Duties and Responsibilities:
Responsible for all aspects of study site monitoring including: routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaising with vendors;
Conducts feasibility work;
Monitors Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs;
Independently performs CRF review; query generation and resolution against data review 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 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, S.O.P.s, GCP;
Good planning, organization and problem solving abilities;
Ability to work with minimal supervision;
Good communication and interpersonal skills;
Good analytical and negotiation skills;
Computer competency;
Fluent in local office language and in English, both written and verbal;
Typ pracy: Permanent
Prosimy o dopisanie następującej klauzuli "Wyrażam zgodę na przetwarzanie moich danych osobowych zawartych w ofercie dla potrzeb procesu rekrutacji zgodnie z Ustawą o ochronie danych osobowych z dnia 29.08.1997r., Dz. U. Nr 101, poz. 926 ze zm." Numer w rejestrze agencji zatrudnienia: 361
Prosimy o dopisanie następującej klauzuli "Wyrażam zgodę na przetwarzanie moich danych osobowych zawartych w ofercie dla potrzeb procesu rekrutacji zgodnie z Ustawą o ochronie danych osobowych z dnia 29.08.1997r., Dz. U. Nr 101, poz. 926 ze zm." Numer w rejestrze agencji zatrudnienia: 361
Miasto: Warszawa, 00-120
Ulica: Złota
Numer domu/mieszkania: 59
Numer telefonu: +48 22 584 5650
Numer faxu: +48 22 584 5651
Adres e-mail: warsaw@hays.pl
Adres strony WWW: http://hays.pl
Ulica: Złota
Numer domu/mieszkania: 59
Numer telefonu: +48 22 584 5650
Numer faxu: +48 22 584 5651
Adres e-mail: warsaw@hays.pl
Adres strony WWW: http://hays.pl

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