Clinical Research Associate

Pracovní nabídka

As a Clinical Research Associate you will have the unique opportunity to have an exciting career in the field of drug and medical device development as part of an expanding team.

Responsibilities:

· Conduct different types of monitoring visits (pre-study visits, site initiation visits, interim monitoring visits & close out visits)

· Develop and maintain site and investigator relationships to ensure clinical trials are managed efficiently

· Perform source document verification and prepare monitoring visit reports, including confirmation and follow-up letter

· Manage the study documentation and other essential trial related documents

· Support regulatory submissions to the Competent Authority

· Participate in Investigator selection/feasibility process

Your profile:

· University degree in a health or life science related field (preferably medical doctor or pharmacist)

· at least 3-year experience as a CRA

· Experience both drug and medical device studies is a plus

· Knowledge of clinical trial protocol and research methodologies

· Skills in clinical operation and monitoring site performance

· Excellent verbal and written communication skills in Czech and English, Slovak is an advantage

· Valid driving license

· Demonstrated flexibility in schedule and willingness to travel on a regular basis

(occasionally 3-4 monitoring visits per week & monthly meeting in the Hungarian Headquarter)

· Ability to respond quickly to changing demands and opportunities

· Detail-oriented and efficient in time management

· Advanced skills and experience using Microsoft Office (Word, Excel, Power Point, Outlook)

We are looking forward to receiving your application with your professional CV in English indicating your salary expectation (monthly, net) via email.