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.
- The position is office based in Budapest, with opportunity for remote workday after completion of 1st year of the training program.
Requirements
- College/University degree in a health or life science related field (preferably medical doctor or pharmacist);
- Excellent verbal and written communication skills in English and Hungarian
- Advanced skills and experience using Microsoft Office (Word, Excel, Power Point, Outlook);
- Valid driving license;
- Demonstrated flexibility in schedule and willingness to travel (60-80% on a regular basis);
- Ability to respond quickly to changing demands and opportunities;
- Detail-oriented and efficient in time management.
Nice-to-have
What we offer
No clinical experience is needed as BiTrial provides comprehensive training including:
- High focus on field-based training;
- Platform to confidently carry out your duties and enhance your professional development to become a high-functioning independent CRA;
- Ongoing support throughout our mentorship program.
Workplace extras
- Bicycle storage
- Parking
- Free coffee, soft drinks
- Free lunch