Descrierea firmei

Avand sediul central in Basel, Elvetia, Roche este una dintre cele mai importante companii farmaceutice bazate pe cercetare si dezvoltare si unul dintre liderii mondiali in domeniul farmaceuticelor si diagnosticelor.

Fiind cea mai mare companie de biotehnologie la nivel mondial, ce ofera produse si servicii inovatoare destinate detectiei precoce, preventiei, diagnosticului si tratamentului bolilor, Grupul Roche contibuie pe o scara larga la imbunatatirea sanatatii si calitatii vietii oamenilor.

Roche este lider mondial in oncologie, transplant si diagnosticare in vitro, lider de piata in virologie si este activ in alte arii terapeutice majore cum ar fi bolile autoimune, bolile inflamatorii, problemele metabolice si bolile sistemului nervos central.

La nivel global Grupul are aproximativ 75.000 de angajati si se mandreste cu faptul ca a creat un mediu de lucru in care fiecare angajat isi poate dezvolta abilitatile, poate contribui pe termen lung la succesul companiei si este real apreciat in conformitate cu activitatea depusa.

Pentru informatii suplimentare, va rugam sa accesati www.roche.com .

Descrierea postului

The position
As a Clinical Research Associate you are responsible for initiating and monitoring local clinical trials and for implementing global clinical studies locally. Part of your work is also to organize investigators meeting and to ensure that the clinical trial facilities and laboratories are adequate for properly conducting the trial in accordance with Roche standards.
The Clinical Research Associate works in close cooperation with Medical Managers and with the Clinical Trials Manager to ensure that the clinical studies are conducted in accordance with the ICH GCP and local regulations. The position reports to the Clinical Trials Manager.

Cerinte

Who are you
You can consider yourself the ideal candidate if you are a medical doctor, you are computer literate, posses very good English language abilities and you are interested for a limited period contract (8 months). You are able to work on numerous and diverse tasks in a simultaneous fashion to meet tight regulatory time frames with a highly variable workload. You are also able to write and communicate complicated matters in a concise and clear way also to non-experts in the field. Other needed abilities for the job are to be able to establish and maintain a network of contacts in the regulatory area, to see signals at an early stage and be pro-active in preventing possible issues. Clean driving licence, B, is a must. Experience in Clinical Research activities is required.

Oferta (bonusuri, beneficii)

What we offer
Roche offers you the possibility to gain experience in a multinational environment. Roche also offers you an attractive compensation package (salary + benefits), high qualitative working tool and the possibility to grow in a competitive and professional environment.

Interested candidates should send their application no later than June 27th, 2008.

Adauga experienta

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