Prijava
Traži
Pregledavate arhivu oglasa objavljenih na www.posao.hr.
Ovaj oglas je istekao 21.03.2012. i više nije aktivan.
Sadržaj oglasa prikazan je isključivo u informativne svrhe.
Trenutno aktivne oglase pogledajte na www.posao.hr.
Ovaj oglas je istekao 21.03.2012. i više nije aktivan.
Sadržaj oglasa prikazan je isključivo u informativne svrhe.
Trenutno aktivne oglase pogledajte na www.posao.hr.
Regional Manager (m/ž)
Oglas je istekao
Poslodavac:
Kategorija:
Mjesto rada:
Zagreb
Rok prijave:
21.03.2012.
O poslu
Opis radnog mjesta:
Sermon CRO is an independent, private company conducting and monitoring clinical trials in South Eastern Europe. Our company has been offering top quality services for foreign pharmaceutical companies for years, and considers the personal effort and creativity of its employees its greatest asset. Sermon CRO has its offices in Zagreb and Belgrade and is currently looking to expand its team. If you like challenges, working in an international environment, travelling and learning, you are an excellent candidate for working in Sermon CRO.
Sermon CRO is currently seeking:
Regional Manager
As a Regional Manager you will be providing input on country and site selection for clinical studies in the region of South East Europe.
You will be responsible for supporting and assisting different CROs in their work on clinical trials, from regulatory, set up and co-ordination of clinical studies (including monitoring and quality control), to assisting CROs and sites with adverse events management and reporting.
Your main focus will be monitoring and reporting the study progress within all ongoing projects, as well as defining the project's objectives and overseeing quality control throughout the project life cycle.
Furthermore, you will be responsible for development of complete CRO oversight Regional Management Plan and ensuring the highest performance and quality in your region through constant cooperation and strong interpersonal relations.
Sermon CRO is currently seeking:
Regional Manager
As a Regional Manager you will be providing input on country and site selection for clinical studies in the region of South East Europe.
You will be responsible for supporting and assisting different CROs in their work on clinical trials, from regulatory, set up and co-ordination of clinical studies (including monitoring and quality control), to assisting CROs and sites with adverse events management and reporting.
Your main focus will be monitoring and reporting the study progress within all ongoing projects, as well as defining the project's objectives and overseeing quality control throughout the project life cycle.
Furthermore, you will be responsible for development of complete CRO oversight Regional Management Plan and ensuring the highest performance and quality in your region through constant cooperation and strong interpersonal relations.
Posebne pogodnosti:
Working environment:
- We offer the possibility of continuous training and professional upgrade through our training system developed with the purpose of exchanging knowledge and experience.
- We maintain good communication with all personnel and on all levels, thus creating a pleasant office environment.
- We conduct regular appraisals and offer attractive remuneration package.
- We offer the possibility of continuous training and professional upgrade through our training system developed with the purpose of exchanging knowledge and experience.
- We maintain good communication with all personnel and on all levels, thus creating a pleasant office environment.
- We conduct regular appraisals and offer attractive remuneration package.
Vrsta posla:
stalni radni odnos
Županija:
O zaposleniku
Znanja i kvalifikacije:
- University degree in medicine, dentistry or pharmacy
- At least three years of experience in working on clinical trials as a monitor and at least two years of experience having a project leadership/management/quality control role
- Active use of English, both spoken and written
- PC literac
- Driving license (category B)
- Excellent interpersonal and communication skills
- Being independent and proactive, systematic and thorough
- Excellent organizational and problem solving skills, goal oriented
- In-depth knowledge of applicable clinical research regulatory requirements
- Willingness to travel
If you believe you are the right person for the above mentioned position, please send your application and CV in English.
- At least three years of experience in working on clinical trials as a monitor and at least two years of experience having a project leadership/management/quality control role
- Active use of English, both spoken and written
- PC literac
- Driving license (category B)
- Excellent interpersonal and communication skills
- Being independent and proactive, systematic and thorough
- Excellent organizational and problem solving skills, goal oriented
- In-depth knowledge of applicable clinical research regulatory requirements
- Willingness to travel
If you believe you are the right person for the above mentioned position, please send your application and CV in English.
Minimalna stručna sprema:
Fakultet
Strani jezik:
engleski
Poznavanje rada na računalu:
dobro
Potrebno radno iskustvo:
tri godine
