Senior Clinical Research Associate – Estonia

Coordinating and monitoring clinical trials in Estonia.

- At least three years experience in coordinating and monitoring clinical trials
- Experience in EC and CA submissions
- Good command of Estonian and English language
- Suitable education for the work
- Good communication skills
- Correctness and responsibility
- Good Computer skills
- Willing to travel

- Work in international company
- Friendly and enthusiastic team
- Compensation package
- Flexible working conditions
- Possibility to work at home


For more information please contact us:
birute.zilaitiene(at)medfiles.eu
Tel. +370 618 22500 or www.medfiles.eu