Klinik Araştırma Saha Görevlisi Comac Medical Ltd Bulgaristan İstanbul Merkez Şubesi

Adana, Afyon, Ankara, Antalya, Bursa, Erzurum, Eskişehir, Gaziantep, Mersin, İstanbul(Avr.), İzmir, Kayseri, Kocaeli, Konya, Malatya, Kahramanmaraş, Samsun, İstanbul(Asya)

Nasıl hesaplanır?
Bu iş sana uygun olmayabilir

Seçili özgeçmişindeki bilgilerle bu ilanın kriterlerleri sadece %30 uyumlu.

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Son iş deneyimin, geçmiş deneyimlerin ve toplam deneyimin uygunluk puanını etkileyen kriterler arasındadır.
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Seçili özgeçmişindeki bilgilerle bu ilanın kriterlerleri sadece %30 uyumlu.

Uygunluğunu nasıl hesapladık?
Mesleki Yeterlilikler
Şirketlerin ilanda belirlediği kriterlerle özgeçmişindeki bilgilerin ne kadar uyumlu olduğu içerik karşılaştırılmasıyla bulunur.
Bu iş sana uygun olmayabilir

Seçili özgeçmişindeki bilgilerle bu ilanın kriterlerleri sadece %30 uyumlu.

Uygunluğunu nasıl hesapladık?
Diğer Bilgiler

QUALIFICATIONS AND JOB DESCRIPTION

COMAC MEDICAL is a Full Service CRO/ SMO providing a broad network of clinical research sites in the best healthcare institutions across Central and Eastern Europe. Due to our successful development we are looking for our new projects in Turkey for highly motivated and responsible candidates for the position of: Clinical Site Coordinator

The Profile:
- Supporting Principal Investigator in equipment and staff needs planning;
- Collection and transfer of site-related documents for initial submission package and ongoing submission package;
- Regular updates of essential documents;
- Assisting in preparation of any study related documents;
- Assisting in CRF completion, when applicable;
- Logistic support related to transfer of information and materials;
- Collaborate with the site team concerning patients pre-screening and recruitment
- Activities related to drug storage, total reconciliation and documents completion;
- Collaborate and facilitate monitor on-site or remote visit;
- Report the trial progress by writing reports and collecting trial-specific data, keeping correspondence, participating in project meetings and teleconferences;
- Financial accountability for patients’ travel expenses;
- First point of contact with CRA/ CRO.

The Person:
- University degree in Medical or Life Sciences is preferable;
- Experience in Clinical Trials activities is preferable;
- Excellent command of English – both written and spoken;
- Excellent computer literacy;
- Active driver;
- Very good attention to details, excellent analytical capabilities;
- Responsible, pro-active, well-organized and committed person, team player;
- Ability to work under pressure and to keep tight deadlines.

The Company Offer:
- Job-specific training;
- Work for a successful international company, excellent career development opportunity in a perspective professional field;
- Competitive and result orientated remuneration;
- Additional benefits related to work performance.

PREFERRED CANDIDATE

POSITION INFORMATION