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Pregledavate arhivu oglasa objavljenih na www.posao.hr.
Ovaj oglas je istekao 25.05.2012. i više nije aktivan.
Sadržaj oglasa prikazan je isključivo u informativne svrhe.
Trenutno aktivne oglase pogledajte na www.posao.hr.
Ovaj oglas je istekao 25.05.2012. i više nije aktivan.
Sadržaj oglasa prikazan je isključivo u informativne svrhe.
Trenutno aktivne oglase pogledajte na www.posao.hr.
Clinical Research Associate - Level II (m/f)
Oglas je istekao
Poslodavac:
Kategorija:
Mjesto rada:
Croatia
Rok prijave:
25.05.2012.
O poslu
Opis radnog mjesta:
PPD was named the best Contract Research Organization at the 2011 Scrip Awards.
PPD is a leading global contract research organization providing drug discovery, development and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. With offices in 45 countries and more than 11 500 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a commitment to quality to help clients and partners accelerate the delivery of safe and effective therapeutics and maximize the returns on their R&D investments.
An exciting opportunity is now available to advance your career as a:
Clinical Research Associate -Level II
The successful candidate will be primarily tasked to set up and monitor clinical trials conducted as part of international projects.
PPD is a leading global contract research organization providing drug discovery, development and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. With offices in 45 countries and more than 11 500 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a commitment to quality to help clients and partners accelerate the delivery of safe and effective therapeutics and maximize the returns on their R&D investments.
An exciting opportunity is now available to advance your career as a:
Clinical Research Associate -Level II
The successful candidate will be primarily tasked to set up and monitor clinical trials conducted as part of international projects.
Posebne pogodnosti:
PPD Offers:
As an equal opportunity employer, PPD believes that employees are the key to its success, and is committed to your professional growth. We offer an attractive salary, comprehensive benefits package as well as bespoke personal development and training programs.
As an equal opportunity employer, PPD believes that employees are the key to its success, and is committed to your professional growth. We offer an attractive salary, comprehensive benefits package as well as bespoke personal development and training programs.
Vrsta posla:
stalni radni odnos
Županija:
Sve županije
O zaposleniku
Znanja i kvalifikacije:
This opportunity is suitable for an experienced in such a position professional with proven experience
Main accountabilities to include but not be limited to:
• Determine protocol and regulatory compliance on the sites.
• You will perform and coordinate all aspects of the clinical monitoring process from "start up" to "close out".
• You should thrive in multi-national project teams and be focused on delivering exemplary levels of customer service.
• You shall be qualified to conduct monitoring activities independently.
Education and Experience:
• Degree in pharmacy, life science or related field.
• At least 2 years of monitoring experience
in interventional studies with a CRO, pharmaceutical or biotech company;
Additional Requirements:
• Demonstrated clinical trial monitoring skills.
• In-depth understanding of ICH/GCP guidelines.
• Excellent standard of verbal and written communication skills in English and Croatian languages.
• Highly organized with strong attention to detail and deadlines.
• Advanced skills across all of the Microsoft packages.
• Willingness to travel;
How to apply:
Please, follow this link in order to submit your application.
Main accountabilities to include but not be limited to:
• Determine protocol and regulatory compliance on the sites.
• You will perform and coordinate all aspects of the clinical monitoring process from "start up" to "close out".
• You should thrive in multi-national project teams and be focused on delivering exemplary levels of customer service.
• You shall be qualified to conduct monitoring activities independently.
Education and Experience:
• Degree in pharmacy, life science or related field.
• At least 2 years of monitoring experience
in interventional studies with a CRO, pharmaceutical or biotech company;
Additional Requirements:
• Demonstrated clinical trial monitoring skills.
• In-depth understanding of ICH/GCP guidelines.
• Excellent standard of verbal and written communication skills in English and Croatian languages.
• Highly organized with strong attention to detail and deadlines.
• Advanced skills across all of the Microsoft packages.
• Willingness to travel;
How to apply:
Please, follow this link in order to submit your application.
Minimalna stručna sprema:
Fakultet
Strani jezik:
engleski
Poznavanje rada na računalu:
napredno
Potrebno radno iskustvo:
dvije godine
